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@Article{ajina.EA:15motion,
author = {Sara Ajina and Christopher Kennard and Geraint Rees
and Holly Bridge},
title = {Motion area {V5/MT+} response to global motion in
the absence of {V1} resembles early visual cortex},
journal = {Brain},
year = 2015,
volume = 138,
pages = {164--178},
note = {dx.doi.org/10.1093/brain/awu328},
abstract = {Motion area V5/MT+ shows a variety of characteristic
visual responses, often linked to perception, which
are heavily influenced by its rich connectivity with
the primary visual cortex (V1). This human motion
area also receives a number of inputs from other
visual regions, including direct subcortical
connections and callosal connections with the
contralateral hemisphere. Little is currently known
about such alternative inputs to V5/MT+ and how they
may drive and influence its activity. Using
functional magnetic resonance imaging, the response
of human V5/MT+ to increasing the proportion of
coherent motion was measured in seven patients with
unilateral V1 damage acquired during adulthood, and
a group of healthy age-matched controls. When V1 was
damaged, the typical V5/MT+ response to increasing
coherence was lost. Rather, V5/MT+ in patients
showed a negative trend with coherence that was
similar to coherence-related activity in V1 of
healthy control subjects. This shift to a
response-pattern more typical of early visual cortex
suggests that in the absence of V1, V5/MT+ activity
may be shaped by similar direct subcortical
input. This is likely to reflect intact residual
pathways rather than a change in connectivity, and
has important implications for blindsight
function. It also confirms predictions that V1 is
critically involved in normal V5/MT+ global motion
processing, consistent with a convergent model of V1
input to V5/MT+. Historically, most attempts to
model cortical visual responses do not consider the
contribution of direct subcortical inputs that may
bypass striate cortex, such as input to V5/MT+. We
have shown that the signal change driven by these
non-striate pathways can be measured, and suggest
that models of the intact visual system may benefit
from considering their contribution.}
}
@Article{ajina.EA:15contr,
author = {Sara Ajina and Geraint Rees and Christopher Kennard
and Holly Bridge},
title = {Abnormal Contrast Responses in the Extrastriate
Cortex of Blindsight Patients},
journal = JoN,
year = 2015,
volume = 35,
number = 21,
pages = {8201--8213},
abstract = {When the human primary visual cortex (V1) is
damaged, the dominant geniculo-striate pathway can
no longer convey visual information to the occipital
cortex. However, many patients with such damage
retain some residual visual function that must rely
on an alternative pathway directly to extrastriate
occipital regions. This residual vision is most
robust for moving stimuli, suggesting a role for
motion area hMT . However, residual vision also
requires high-contrast stimuli, which is
inconsistent with hMT sensitivity to contrast in
which even low-contrast levels elicit near-maximal
neural activation. We sought to investigate this
discrepancy by measuring behavioral and neural
responses to increasing contrast in patients with V1
damage. Eight patients underwent behavioral testing
and functional magnetic resonance imaging to record
contrast sensitivity in hMT of their damaged
hemisphere, using Gabor stimuli with a spatial
frequency of 1 cycle/°. The responses from hMT of
the blind hemisphere were compared with hMT and V1
responses in the sighted hemisphere of patients and
a group of age-matched controls. Unlike hMT , neural
responses in V1 tend to increase linearly with
increasing contrast, likely reflecting a dominant
parvocellular channel input. Across all patients,
the responses in hMT of the blind hemisphere no
longer showed early saturation but increased
linearly with contrast. Given the spatiotemporal
parameters used in this study and the known direct
subcortical projections from the koniocellular
layers of the lateral geniculate nucleus to hMT , we
propose that this altered contrast sensitivity in
hMT could be consistent with input from the
koniocellular pathway.}
}
@Article{ajina.EA:15dMRI,
author = {Sara Ajina and Franco Pestilli and Ariel Rokem and
Christopher Kennard and Holly Bridge},
title = {Human blindsight is mediated by an intact
geniculo-extrastriate pathway},
journal = {eLIFE},
year = 2015,
volume = 4,
pages = {e08935},
note = {10.7554/eLife.08935},
abstract = {Although damage to the primary visual cortex (V1)
causes hemianopia, many patients retain some
residual vision; known as blindsight. We show that
blindsight may be facilitated by an intact
white-matter pathway between the lateral geniculate
nucleus and motion area hMT+. Visual psychophysics,
diffusion-weighted magnetic resonance imaging and
fibre tractography were applied in 17 patients with
V1 damage acquired during adulthood and 9
age-matched controls. Individuals with V1 damage
were subdivided into blindsight positive (preserved
residual vision) and negative (no residual vision)
according to psychophysical performance. All
blindsight positive individuals showed intact
geniculo-hMT+ pathways, while this pathway was
significantly impaired or not measurable in
blindsight negative individuals. Two white matter
pathways previously implicated in blindsight: (i)
superior colliculus to hMT+ and (ii) between hMT+ in
each hemisphere were not consistently present in
blindsight positive cases. Understanding the visual
pathways crucial for residual vision may direct
future rehabilitation strategies for hemianopia
patients. }
}
@Article{anwar.EA:09,
author = {Muhammad Nabeel Anwar and Laura Bonzano and Davide
Rossi Sebastiano and Luca Roccatagliata and Giovanni
Gualniera and Paolo Vitali and Carla Ogliastro and
Luciano Spadavecchia and Guido Rodriguez and
Vittorio Sanguineti and Pietro Morasso and Fabio
Bandini},
title = { Real-time artifact filtering in continuous
{VEPs/fMRI} recording},
journal = JNMeth,
year = 2009,
volume = 184,
pages = 184,
abstract = {Continuous recording of Visual Evoked Potentials
(VEPs) and functional Magnetic Resonance Imaging
(fMRI) exploits the VEPs high temporal resolution
and the fMRI high spatial resolution. In this work,
we present a new method of continuous VEPs/fMRI
recording to study visual function in seven normal
subjects. Our real-time artifact filtering is
characterized by a procedure based on an analytical
study of echo-planar imaging (EPI) sequence
parameters related electro-encephalogram
(EEG)-artifact shapes. The magnetic field artifacts
were minimized by using a dedicated amagnetic device
and by a subtraction algorithm that takes into
account the EPI sequence parameters. No significant
decrease in signal-to-noise ratio was observed in
case of EEG recording simultaneously with MR
acquisition; similarly, transient and steady-state
VEPs parameters were comparable during fMRI
acquisition and in the off-phase of fMRI
recording. We also applied this method to one
patient with optic neuritis, and, compared with
controls, found different results. We suggest that
our technique can be reliably used to investigate
the function of human visual cortex and properly
correlate the electrophysiological and functional
neuroimaging related changes.}
}
@Article{azzopardi.hock:11,
author = {Paul Azzopardi and Howard S. Hock},
title = {Illusory motion perception in blindsight},
journal = PNAS,
year = 2011,
volume = 108,
number = 2,
pages = {876--881},
abstract = {Motion detection is typically spared in blindsight,
which results from damage to the striate cortex
(area V1) of the brain that is sufficient to
eliminate conscious visual awareness and severely
reduce sensitivity to luminance contrast, especially
for high spatial and low temporal frequencies. Here
we show that the discrimina- tion of motion
direction within cortically blind fields is not
attributable to feature tracking (the detection of
changes in position or shape), but is due instead to
the detection of first- order motion energy
(spatiotemporal changes in luminance). The key to
this finding was a version of the line motion
illusion entailing reverse-phi motion in which
opposing motion directions are simultaneously cued
by motion energy and changes in stimulus shape. In
forced-choice tests, a blindsighted test subject
selected the direction cued by shape change when the
stimulus was presented in his intact field, but
reliably selected the direction cued by motion
energy when the same stimulus was presented in his
blind field, where relevant position information was
either inaccessible or invalid. Motion energy has
been characterized as objectless, so reliance on
motion energy detection is consistent with impaired
access to shape information in blindsight. The
dissociation of motion direction by visual field
(cortically blind vs. intact) provides evidence that
two pathways from the retina to MT/V5 (the cortical
area specialized for motion perception) are
functionally distinct: the retinogeniculate pathway
through V1 is specialized for feature-based motion
perception, whereas the retinocollicular pathway,
which bypasses V1, is specialized for detecting
motion energy.}
}
@Article{he.EA:11,
author = {Bin He and Yakang Dai and Laura Astolfi and Fabio
Babiloni and Han Yuan and Lin Yang},
title = {{eConnectome: A MATLAB} toolbox for mapping and
imaging of brain functional connectivity},
journal = JNMeth,
year = 2011,
volume = 195,
number = 2,
pages = {261--269},
abstract = {We have developed a MATLAB-based toolbox,
eConnectome (electrophysiological connectome), for
mapping and imaging functional connectivity at both
the scalp and cortical levels from the
electroencephalogram (EEG), as well as from the
electrocorticogram (ECoG). Graphical user interfaces
were designed for interactive and intuitive use of
the toolbox. Major functions of eConnectome include
EEG/ECoG preprocessing, scalp spatial mapping,
cortical source estimation, connectivity analysis,
and visualization. Granger causality measures such
as directed transfer function and adaptive directed
transfer function were implemented to estimate the
directional interactions of brain functional
networks, over the scalp and cortical sensor
spaces. Cortical current density inverse imaging was
implemented using a generic realistic geometry
brain–head model from scalp EEGs. Granger causality
could be further estimated over the cortical source
domain from the inversely reconstructed cortical
source signals as derived from the scalp EEG. Users
may implement other connectivity estimators in the
framework of eConnectome for various
applications. The toolbox package is open-source and
freely available at http://econnectome.umn.edu under
the GNU general public license for noncommercial and
academic uses.}
}
@Article{hindiattar.EA:10,
author = {Catherine {Hindi Attar} and S{\/o}ren K. Andersen and
Matthias M. M{\"u}ller},
title = {Time course of affective bias in visual attention:
Convergent evidence from steady-state visual evoked
potentials and behavioral data},
journal = NI,
year = 2010,
volume = 53,
pages = {1326--1333},
abstract = {Selective attention to a primary task can be biased
by the occurrence of emotional distractors that
involuntary attract attention due to their intrinsic
stimulus significance. What is largely unknown is
the time course and magnitude of competitive
interactions between a to-be-attended foreground
task and emotional distractors. We used pleasant,
unpleasant and neutral pictures from the
International Affective Picture System (IAPS) that
were either presented in intact or phase-scrambled
form. Pictures were superimposed by a flickering
display of moving random dots, which constituted the
primary task and enabled us to record steady-state
visual evoked potentials (SSVEPs) as a continuous
measure of attentional resource allocation directed
to the task. Subjects were required to attend to the
dots and to detect short intervals of coherent
motion while ignoring the background pictures. We
found that pleasant and unpleasant relative to
neutral pictures more strongly influenced
task-related processing as reflected in a
significant decrease in SSVEP amplitudes and target
detection rates, both covering a time window of
several hundred milliseconds. Strikingly, the effect
of semantic relative to phase-scrambled pictures on
task-related activity was much larger, emerged
earlier and lasted longer in time compared to the
specific effect of emotion. The observed differences
in size and duration of time courses of semantic and
emotional picture processing strengthen the
assumption of separate functional mechanisms for
both processes rather than a general boosting of
neural activity in favor of emotional stimulus
processing.}
}
@Article{bagattini.EA:15,
author = {Chiara Bagattini and Chiara Mazzi and Silvia
Savazzi},
title = {Waves of awareness for occipital and parietal
phosphenes perception},
journal = {Neuropsychologia},
year = 2015,
volume = 70,
pages = {114--125},
abstract = {Transcranial magnetic stimulation (TMS) of the
occipital cortex is known to induce visual
sensations, i.e. phosphenes, which appear as fl
ashes of light in the absence of an external
stimulus. Recent studies have shown that TMS can
produce phosphenes also when the intraparietal
sulcus (IPS) is stimulated. The main question
addressed in this paper is whether parietal
phosphenes are generated directly by local me-
chanisms or emerge through indirect activation of
other visual areas. Electroencephalographic (EEG)
signals were recorded while stimulating left
occipital or parietal cortices inducing phosphene
perception in healthy participants and in a
hemianopic patient who suffered from complete
destruction of the early visual cortex of the left
hemisphere. Results in healthy participants showed
that the onset of phosphene perception induced by
occipital TMS correlated with differential cortical
activity in temporal sites while the onset of
phosphene perception induced by parietal TMS
correlated with differential cortical activity in
the stimulated parietal site. Moreover, IPS-TMS of
the lesioned hemisphere of the hemianopic patient
with a complete lesion to V1 showed again that the
onset of phosphene perception correlated with
differential cortical activity in the stimulated
parietal site. The present data seem thus to suggest
that temporal and parietal cortices can serve as
different local early gatekeepers of perceptual
awareness and that activity in the occipital cortex,
although being relevant for perception in general,
is not part of the neural bases of the perceptual
awareness of phosphenes.}
}
@Article{bandettini.cox:00,
author = {Peter A. Bandettini and Robert W. Cox},
title = {Event-Related {fMRI} Contrast When Using Constant
Interstimulus Interval: Theory and Experiment},
journal = MRM,
year = 2000,
volume = 43,
pages = {540--548},
annote = {Event-related functional magnetic resonance imaging
(ER- fMRI) involves the mapping of averaged
hemodynamic changes resulting from repeated, brief (
< 3 sec) brain activation epi- sodes. In this paper,
two issues regarding constant-interstimu- lus
interval ER-fMRI were addressed. First, the optimal
inter- stimulus interval (ISI), given a stimulus
duration (SD), was de- termined. Second, the
statistical power of ER-fMRI relative to that of a
blocked-design paradigm was determined. Experimen-
tally, it was found that with a 2-sec SD, the
optimal ISI is 12 to 14 sec. Theoretically, the
optimal repetition interval ( T opt 5 ISI 1 SD) is
12 to 14 sec for stimuli of 2 sec or less. For
longer stimuli, T opt is 8+2 * SD. At the optimal
ISI for SD=2 sec, the experimentally determined
functional contrast of ER-fMRI was only 2 35% lower
than that of blocked-design fMRI. Simulations that
assumed a linear system demonstrated an
event-related functional contrast that was 2 65%
lower than that of the blocked design. These
differences between simulated and ex- perimental
contrast suggest that the ER-fMRI amplitude is
greater than that predicted by a linear
shift-invariant system.}
}
@Article{barbur.EA:93,
author = {J. L. Barbur and J. D. G. Watson and R. S. J.
Frackowiak and S. Zeki},
title = {Conscious visual perception without {VI}},
journal = {Brain},
year = 1993,
volume = 116,
pages = {1293--1302},
abstract = {We used the technique of PET to determine whether
visual signals reach visual area V5, specialized for
visual motion, when a human patient, blinded by a
lesion in area VI, discriminates the direction of
motion of visual stimuli and shows, through his
verbal reports, that he is consciously aware of both
the nature of the visual stimulus and its direction
of motion. The results showed that area V5 was
active without a parallel activation of area VI,
implying that the visual input can reach V5 without
passing first through VI and that such an input is
sufficient for both the discrimination and the
conscious awareness of the visual stimulus.}
}
@Article{bayram.EA:11,
author = {Ali Bayram and Zubeyir Bayraktaroglu and Esin
Karahan and Basri Erdogan and Basar Bilgic and Muge
Özker and Itir Kasikci and Adil D. Duru and Ahmet
Ademoglu and Cengizhan {\"O}zt{\"u}rk and Kemal
Arikan and Nevzat Tarhan and Tamer Demiralp},
title = {Simultaneous {EEG/fMRI} Analysis of the Resonance
Phenomena in {Steady-State Visual Evoked Responses}},
journal = CEEGN,
year = 2011,
volume = 42,
number = 2,
pages = {98--106},
annote = {The stability of the steady-state visual evoked
potentials (SSVEPs) across trials and subjects makes
them a suitable tool for the investigation of the
visual system. The reproducible pattern of the
frequency charac- teristics of SSVEPs shows a global
amplitude maximum around 10 Hz and additional local
maxima around 20 and 40 Hz, which have been argued
to represent resonant behavior of damped neuronal
oscillators. Simultaneous
electroencephalogram/functional magnetic reson- ance
imaging (EEG/fMRI) measurement allows testing of the
reson- ance hypothesis about the frequency-selective
increases in SSVEP amplitudes in human subjects,
because the total synaptic activity that is
represented in the fMRI-Blood Oxygen Level Dependent
(fMRI- BOLD) response would not increase but get
synchronized at the resonance frequency. For this
purpose, 40 healthy volunteers were visually
stimulated with flickering light at systematically
varying frequencies between 6 and 46 Hz, and the
correlations between SSVEP amplitudes and the BOLD
responses were computed. The SSVEP frequency
characteristics of all subjects showed 3 frequency
ranges with an amplitude maximum in each of them,
which roughly correspond to alpha, beta and gamma
bands of the EEG. The correlation maps between BOLD
responses and SSVEP amplitude changes across the
different stimulation frequencies within each
frequency band showed no significant correlation in
the alpha range, while significant correlations were
obtained in the primary visual area for the beta and
gamma bands. This non-linear relationship between
the surface recorded SSVEP amplitudes and the BOLD
responses of the visual cortex at stimulation
frequencies around the alpha band supports the view
that a resonance at the tuning frequency of the
thalamo-cortical alpha oscillator in the visual
system is responsible for the global amplitude
maximum of the SSVEP around 10 Hz. Information
gained from the SSVEP/fMRI analyses in the present
study might be extrapolated to the EEG/fMRI analysis
of the transient event-related potentials (ERPs) in
terms of expecting more reliable and consistent
correlations between EEG and fMRI responses, when
the analyses are carried out on evoked or induced
oscillations (spectral perturbations) in separate
frequency bands instead of the time-domain ERP
peaks.}
}
@Article{becker.EA:10,
author = {Stefanie I. Becker and Charles L. Folk and Roger
W. Remington},
title = {The Role of Relational Information in Contingent
Capture},
journal = JEPhpp,
year = 2010,
volume = 36,
number = 6,
pages = {1460--1476},
abstract = {On the contingent capture account, top-down
attentional control settings restrict involuntary
attentional capture to items that match the features
of the search target. Attention capture is
involuntary, but contingent on goals and
intentions. The observation that only target-similar
items can capture attention has usually been taken
to show that the content of the attentional control
settings consists of specific feature values. In
contrast, the present study demonstrates that the
top-down target template can include information
about the relationship between the target and
nontarget features (e.g., redder, darker,
larger). Several spatial cuing experiments show that
a singleton cue that is less similar to the target
but that shares the same relational property that
distinguishes targets from nontargets can capture
attention to the same extent as cues that are
similar to the target. Moreover, less similar cues
can even capture attention more than cues that are
identical to the target when they are relationally
better than identical cues. The implications for
current theories of attentional capture and
attentional guidance are discussed.}
}
@Article{benoni.tsal:10,
author = {Hanna Benoni and Yehoshua Tsal},
title = {Where have we gone wrong? Perceptual load does not
affect selective attention},
journal = VisRes,
year = 2010,
volume = 50,
pages = {1292--1298},
abstract = {The theory of perceptual load (Lavie & Tsal, 1994)
proposes that with low load in relevant processing
left over resources spill over to process irrelevant
distractors. Interference could only be prevented
under High-Load Conditions where relevant processing
exhausts attentional resources. The theory is based
primarily on the finding that distractor
interference obtained in low load displays, when the
target appears alone, is eliminated in high load
displays when it is embedded among neutral
letters. However, a possible alternative
interpretation of this effect is that the distractor
is similarly processed in both displays, yet its
interference in the large displays is diluted by the
presence of the neutral letters. We separated the
possible effects of load and dilution by adding
dilution displays that were high in dilution and low
in perceptual load. In the first experiment these
displays contained as many letters as the high load
displays, but their neutral letters were clearly
distinguished from the target, thereby allowing for
a low load processing mode. In the second experiment
we presented identical multicolor displays in the
Dilution and High-Load Conditions. However, in the
former the target color was known in advance
(thereby preserving a low load processing mode)
whereas in the latter it was not. In both
experiments distractor interference was completely
eliminated under the Dilution Condition. Thus, it is
dilution not perceptual load affecting distractor
processing.}
}
@Article{benson.EA:98,
author = {Philip J. Benson and Kun Guo and Colin Blakemore},
title = {Direction discrimination of moving gratings and
plaids and coherence in dot displays without primary
visual cortex ({V1}).},
journal = EJN,
year = 1998,
volume = 10,
number = 12,
pages = {3767--3772},
abstract = {We present new experimental observations of G.Y., a
well-tested patient with unilateral loss of primary
visual cortex. We stimulated G.Y.'s blind hemifield
using first- and second-order motion stimuli at
velocities around psychophysical threshold. Using a
dual response paradigm (awareness level of visual
motion, motion direction discrimination)
psychophysical performance improved with increasing
velocity and dot coherence. We were also able to
influence directly G.Y.'s performance for the better
and at will, by placing the emphasis solely on
direction discrimination. In the absence of V1,
graduated detection and discrimination of stimuli
known to activate both V1 and extrastriate motion
areas MT/V5 and MST is still possible. These results
are in line with residual visual processing but did
not show evidence of unconscious processing of
motion stimuli characteristic of 'blindsight'.}
}
@Article{bertoldi.EA:15,
author = {F. de Bertoldi and L. Finos and M. Maieron and
L. Weis and M. Campanella and T. Ius and L. Fadiga},
title = {Improving the reliability of single-subject {fMRI}
by weighting intra-run variability},
journal = NI,
year = 2015,
volume = 114,
pages = {287--293},
abstract = {At present, functional magnetic resonance imaging
(fMRI) is one of the most useful methods of studying
cogni- tive processes in the human brain in vivo,
both for basic science and clinical goals. Although
neuroscience studies often rely on group analysis,
clinical applications must investigate single
subjects (patients) only. Particularly for the
latter, issues regarding the reliability of fMRI
readings remain to be resolved. To determine the
ability of intra- run variability (IRV) weighting to
consistently detect active voxels, we first acquired
fMRI data from a sample of healthy subjects, each of
whom performed 4 runs (4 blocks each) of self-paced
finger-tapping. Each subject's data was analyzed
using single-run general linear model (GLM), and
each block was then analyzed separately to calculate
the IRV weighting. Results show that integrating IRV
information into standard single-subject GLM
activation maps significantly improved the
reliability (p = 0.007) of the single-subject fMRI
data. This suggests that taking IRV into account can
help identify the most constant and relevant
neuronal activity at the single- subject level.}
}
@Article{bianciardi.EA:09,
author = {M. Bianciardi and L. Bianchi and G. Garreffa and
M. Abbafati and F. {Di Russo} and M.G. Marciani and
E. Macaluso},
title = {Single-epoch analysis of interleaved evoked
potentials and fMRI responses during steady-state
visual stimulation},
journal = ClinNeurophys,
year = 2009,
volume = 120,
pages = {738--747},
abstract = {Objective: Aim of the study was to record BOLD-fMRI
interleaved with evoked potentials for single-
epochs of visual stimulation and to investigate the
possible relationship between these two
measures. Methods: Sparse recording of fMRI and EEG
allowed us to measure BOLD responses and evoked
potentials on an epoch-by-epoch basis. To obtain
robust estimates of evoked potentials, we used
blocks of contrast- reversing visual stimuli
eliciting steady-state visual evoked potentials
(SSVEPs). For each block we acquired one volume of
fMRI data and we then tested for co-variations
between SSVEPs and fMRI signals. Our analyses tested
for frequency-specific co-variation between the two
measurements that could not be explained by the mere
presence/absence of the visual stimulation.
Results: Condition-specific single-epoch SSVEPs and
fMRI responses were observed at occipital
sites. Combined SSVEPs–fMRI analysis at the
single-epoch level did not reveal any significant
correlation between the two recordings. However,
both signals contained stimulation-specific linear
decreases that may relate to neuronal habituation.
Conclusions: Our findings demonstrate robust
estimation of single-epoch evoked potentials and
fMRI responses during interleaved recording, using
visual steady-state stimulation. Significance:
Single-epochs analysis of evoked potentials and fMRI
signals is feasible for interleaved SSVEPs–fMRI
recordings.}
}
@Article{bittar.EA:99,
author = {R.G. Bittar and M. Ptito and J. Faubert and
S.O. Dumoulin and A. Ptito},
title = {Activation of the Remaining Hemisphere Following
Stimulation of the Blind Hemifield in
Hemispherectomized Subjects},
journal = NI,
year = 1999,
volume = 10,
number = 3,
pages = {339--346},
abstract = {We used functional magnetic resonance imaging (fMRI)
to investigate the neural substrates mediating
residual vision in the “blind” hemifield of
hemispherectomized patients. The visual stimuli were
semicircular gratings moving in opposite directions
on a dynamic random-dot background. They were
specifically constructed to eliminate intra- and
extraocular light scatter and optimize the
activation of extrastriate cortical areas and their
subcortical relays. Multislice T2*-weighted gradient
echo (GE) echoplanar imaging (EPI) images (TR/TE = 4
s/45 ms, flip angle 90°) were acquired during
activation and baseline visual stimulation. An
activation minus baseline subtraction was performed,
and the acquired t statistic map transformed into
the stereotaxic coordinate space of Talairach and
Tournoux. In seven normal control subjects, right
hemifield stimulation produced significant
activation foci in contralateral V1/V2, V3/V3A, VP,
and V5 (MT). Significant activation was also
produced in homologous regions of the right
occipital lobe with left hemifield
stimulation. Stimulation of the intact hemifield in
hemispherectomized patients resulted in activation
of similar areas exclusively within the
contralateral hemisphere. Stimulation of the anopic
hemifield produced statistically significant
activation in the ipsilateral occipital lobe
(putative area V5 or MT) and areas V3/V3A in the
only subject with blindsight. We conclude that the
remaining hemisphere may contribute to residual
visual functions in the blind hemifield of
hemispherectomized patients, possibly through the
collicular–pulvinar route since the activated areas
are known to receive their afferents from these
subcortical nuclei.}
}
@Article{block:11,
author = {Ned Block},
title = {Perceptual consciousness overflows cognitive access},
journal = TIC,
year = 2011,
volume = 15,
number = 12,
pages = {567--575},
abstract = {One of the most important issues concerning the
foun- dations of conscious perception centers on the
question of whether perceptual consciousness is rich
or sparse. The overflow argument uses a form of
‘iconic memory’ to argue that perceptual
consciousness is richer (i.e., has a higher
capacity) than cognitive access: when observ- ing a
complex scene we are conscious of more than we can
report or think about. Recently, the overflow argu-
ment has been challenged both empirically and
concep- tually. This paper reviews the controversy,
arguing that proponents of sparse perception are
committed to the postulation of (i) a peculiar kind
of generic conscious representation that has no
independent rationale and (ii) an unmotivated form
of unconscious representation that in some cases
conflicts with what we know about unconscious
representation. }
}
@Article{bordier.EA:15,
author = {C{\'e}cile Bordier and Jean-MichelHup{\'e} and
Michel Dojat},
title = {Quantitative evaluation of {fMRI} retinotopic maps,
from V1 to V4, for cognitive experiments},
journal = FHN,
year = 2015,
volume = 9,
number = 277,
note = {doi:10.3389/fnhum.2015.00277},
abstract = {FMRI retinotopic mapping is a non-invasive technique
for the delineation of low-level visual areas in
individual subjects. It generally relies upon the
analysis of functional responses to periodic visual
stimuli that encode eccentricity or polar angle in
the visual field. This technique is used in vision
research when the precise assignation of brain
activation to retinotopic areas is an issue. It
involves processing steps computed with different
algorithms and embedded in various software
suites. Manual intervention may be needed for some
steps. Although the diversity of the available
processing suites and manual interventions may
potentially introduce some differences in the final
delineation of visual areas, no documented
comparison between maps obtained with different
procedures has been reported in the literature. To
explore the effect of the processing steps on the
quality of the maps obtained, we used two tools,
BALC, which relies on a fully automated procedure,
and BrainVoyager, where areas are delineated “by
hand” on the brain surface. To focus on the mapping
procedures specifically, we used the same SPM
pipeline for pretreatment and the same tissue
segmentation tool. We document the consistency and
differences of the fMRI retinotopic maps obtained
from “routine retinotopy” experiments on 10
subjects. The maps obtained by skilled users are
never fully identical. However, the agreement
between the maps, around 80% for low-level areas, is
probably sufficient for most applications. Our
results also indicate that assigning cognitive
activations, following a specific experiment (here,
color perception), to individual retinotopic maps is
not free of errors. We provide measurements of this
error, that may help for the cautious interpretation
of cognitive activation projection onto fMRI
retinotopic maps. On average, the magnitude of the
error is about 20%, with much larger differences in
a few subjects. More variability may even be
expected with less trained users or using different
acquisition parameters and preprocessing chains.}
}
@Article{brett.EA:01,
author = {Matthew Brett and Alexander P. Leff and Chris Rorden
and John Ashburner},
title = {Spatial Normalization of Brain Images with Focal
Lesions Using Cost Function Masking},
journal = NI,
year = 2001,
volume = 14,
number = 2,
pages = {486--500},
abstract = {In studies of patients with focal brain lesions, it
is often useful to coregister an image of the
patient's brain to that of another subject or a
standard template. We refer to this process as
spatial normalization. Spatial normalization can
improve the presentation and analysis of lesion
location in neuropsychological studies; it can also
allow other data, for example from functional
imaging, to be compared to data from other patients
or normal controls. In functional imaging, the
standard procedure for spatial normalization is to
use an automated algorithm, which minimizes a
measure of difference between image and template,
based on image intensity values. These algorithms
usually optimize both linear (translations,
rotations, zooms, and shears) and nonlinear
transforms. In the presence of a focal lesion,
automated algorithms attempt to reduce image
mismatch between template and image at the site of
the lesion. This can lead to significant
inappropriate image distortion, especially when
nonlinear transforms are used. One solution is to
use cost-function masking—masking the areas used in
the calculation of image difference—to exclude the
area of the lesion, so that the lesion does not bias
the transformations. We introduce and evaluate this
technique using normalizations of a selection of
brains with focal lesions and normal brains with
simulated lesions. Our results suggest that
cost-function masking is superior to the standard
approach to this problem, which is affine-only
normalization; we propose that cost-function masking
should be used routinely for normalizations of
brains with focal lesions.}
}
@Article{bridge.EA:08,
author = {Holly Bridge and Owen Thomas and Saâd Jbabdi and
Alan Cowey},
title = {Changes in connectivity after visual cortical brain
damage underlie altered visual function},
journal = {Brain},
year = 2008,
volume = 131,
number = 6,
pages = {1433--1444},
abstract = {The full extent of the brain's ability to compensate
for damage or changed experience is yet to be
established. One question particularly important for
evaluating and understanding rehabilitation
following brain damage is whether recovery involves
new and aberrant neural connections or whether any
change in function is due to the functional
recruitment of existing pathways, or
both. Blindsight, a condition in which subjects with
complete destruction of part of striate cortex (V1)
retain extensive visual capacities within the
clinically blind field, is an excellent example of
altered visual function. Since the main pathway to
the visual cortex is destroyed, the spared or
recovered visual ability must arise from either an
existing alternative pathway, or the formation of a
new pathway. Using diffusion-weighted MRI, we show
that both controls and blindsight subject GY, whose
left V1 is destroyed, show an ipsilateral pathway
between LGN (lateral geniculate nucleus) and human
motion area MT+/V5 (bypassing V1). However, in
addition, GY shows two major features absent in
controls: (i) a contralateral pathway from right LGN
to left MT+/V5, (ii) a substantial cortico-cortical
connection between MT+/V5 bilaterally. Both
observations are consistent with previous functional
MRI data from GY showing enhanced ipsilateral
activation in MT+/V5. There is also evidence for a
pathway in GY from left LGN to right MT+/V5,
although the lesion makes its quantification
difficult. This suggests that employing alternative
brain regions for processing of information
following cortical damage in childhood may
strengthen or establish specific connections.}
}
@Article{bridge.EA:10,
author = {Holly Bridge and Stephen L. Hicks and Jingyi Xie and
Thomas W. Okell and Sabira Mannan and Iona Alexander
and Alan Cowey and Christopher Kennard},
title = {Visual activation of extra-striate cortex in the
absence of {V1} activation},
journal = {Neuropsychologia},
year = 2010,
volume = 48,
pages = {4148--4154},
abstract = {When the primary visual cortex (V1) is damaged,
there are a number of alternative pathways that can
carry visual information from the eyes to
extrastriate visual areas. Damage to the visual
cortex from trauma or infarct is often unilateral,
extensive and includes gray matter and white matter
tracts, which can disrupt other routes to residual
visual function. We report an unusual young patient,
SBR, who has bilateral damage to the gray matter of
V1, sparing the adjacent white matter and
surrounding visual areas. Using functional magnetic
resonance imaging (fMRI), we show that area MT+/V5
is activated bilaterally to visual stimulation,
while no significant activity could be measured in
V1. Additionally, the white matter tracts between
the lateral geniculate nucleus (LGN) and V1 appear
to show some degeneration, while the tracts between
LGN and MT+/V5 do not differ from
controls. Furthermore, the bilateral nature of the
damage suggests that residual visual capacity does
not result from strengthened interhemispheric
connections. The very specific lesion in SBR
suggests that the ipsilateral connection between LGN
and MT+/V5 may be important for residual visual
function in the presence of damage to V1.}
}
@Article{brown.roosgilbert:95,
author = {Tracy L. Brown and Linda Roos-Gilbert},
title = {Automaticity and word perception: Evidence from
Stroop and Stroop dilution effects},
journal = JEPlmc,
year = 1995,
volume = 95,
number = 21,
pages = 1395,
annote = {DON'T HAVE PAPER},
abstract = {Examines the theory that word perception is
automatic. Role of the automatic nature of word
perception in theories of reading skill; Stroop and
Stroop dilution effects as a source of support for
the automaticity of word perception; Alternative
explanations of Stroop dilution; Attention capture;
Presentation of neutral words at fixation; Early
visual interference account.}
}
@Article{bullier:01,
author = {Jean Bullier},
title = {Integrated model of visual processing},
journal = BRR,
year = 2001,
volume = 36,
number = {2--3},
pages = {96--107},
abstract = {Cortical processing of visual information requires
that information be exchanged between neurons coding
for distant regions in the visual field. It is
argued that feedback connections are the best
candidates for such rapid long-distance
interconnections. In the integrated model,
information arriving in the cortex from the
magnocellular layers of the lateral geniculate
nucleus is first sent and processed in the parietal
cortex that is very rapidly activated by a visual
stimulus. Results from this first-pass computation
are then sent back by feedback connections to areas
V1 and V2 that act as ‘active black-boards’ for the
rest of the visual cortical areas: information
retroinjected from the parietal cortex is used to
guide further processing of parvocellular and
koniocellular information in the inferotemporal
cortex.}
}
@Article{calderone.EA:13,
author = {Daniel J. Calderone and Antígona Martinez and Vance
Zemon and Matthew J. Hoptman and George Hu and Jade
E. Watkins and Daniel C. Javitt and Pamela
D. Butler},
title = {Comparison of psychophysical, electrophysiological,
and {fMRI} assessment of visual contrast responses
in patients with schizophrenia},
journal = NI,
year = 2013,
volume = 67,
pages = {153--162},
abstract = {Perception has been identified by the NIMH-sponsored
Cognitive Neuroscience Treatment Research to Improve
Cognition in Schizophrenia (CNTRICS) group as a
useful domain for assessing cognitive deficits in
patients with schizophrenia. Specific measures of
contrast gain derived from recordings of
steady-state visual evoked potentials (ssVEP) have
demonstrated neural deficits within the visual
pathways of patients with
schizophrenia. Psychophysical measures of contrast
sensitivity have also shown functional loss in these
pa- tients. In the current study, functional
magnetic resonance imaging (fMRI) was used in
conjunction with ssVEP and contrast sensitivity
testing to elucidate the neural underpinnings of
these deficits. During fMRI scanning, participants
viewed 1) the same low and higher spatial frequency
stimuli used in the psychophys- ical contrast
sensitivity task, at both individual detection
threshold contrast and at a high contrast; and 2)
the same stimuli used in the ssVEP paradigm, which
were designed to be biased toward either the
magnocellular or parvocellular visual
pathway. Patients showed significant impairment in
contrast sensitivity at both spatial frequencies in
the psychophysical task, but showed reduced
occipital activation volume for low, but not higher,
spatial frequency at the low and high contrasts
tested in the magnet. As expected, patients
exhibited selective deficits under the
magnocellular-biased ssVEP condition. However,
occipital lobe fMRI responses demonstrated the same
general pattern for magnocellular- and
parvocellular-biased stimuli across groups. These
results indicate dissociation between the fMRI
measures and the psychophysical/ssVEP
measures. These latter measures appear to have
greater value for the functional assessment of the
contrast deficits ex- plored here.}
}
@Article{celeghin.EA:15RT,
author = {Alessia Celeghin and Marissa Barabas and Francesca
Mancini and Matteo Bendini and Emilio Pedrotti and
Massimo Prior and Anna Cantagallo and Silvia Savazzi
and Carlo A. Marzi},
title = {Speeded manual responses to unseen visual stimuli in
hemianopic patients: What kind of blindsight?},
journal = ConscCog,
year = 2015,
volume = 32,
pages = {6--14},
abstract = {Blindsight, i.e., unconscious visually guided
behaviour triggered by stimuli presented to a
cortically blind hemifield, has been typically found
either by using direct (forced choice) or indirect
(interhemispheric) methods. However, one would
expect to find blindsight also in fast responses to
suddenly appearing visual stimuli, a reminiscence of
evolutionary ancient adaptive behaviour. In this
study we provide preliminary evidence of this form
of blindsight by using a conservative method for
assessing blindsight based on a comparison between
the cumulative probability functions (CPFs) of
simple reaction times to blind and intact field
stimuli. Furthermore, in two patients with
blindsight we provided evidence that their
above-chance unconscious responses were likely to be
triggered by the intact hemisphere.}
}
@Article{celeghin.EA:15,
author = {Alessia Celeghin and Silvia Savazzi and Marissa
Barabas and Matteo Bendini and Carlo A. Marzi},
title = {Blindsight is sensitive to stimulus numerosity and
configuration: evidence from the redundant signal
effect},
journal = EBR,
year = 2015,
volume = 233,
number = 5,
pages = {1617--1623},
annote = {One important, yet relatively unexplored ques- tion
is whether blindsight, i.e., unconscious visually
guided behavior in hemianopic patients, is endowed
with basic perceptual properties such as detecting
stimulus numerosity and overall
configuration. Rather than a forced-choice pro-
cedure in which patients are supposed to guess about
stim- uli presented to the blind hemifield, we used
a redundant signal effect paradigm, i.e., the
speeding of simple reaction time (RT) when
presenting multiple versus single similar
stimuli. The presence of an effect of numerosity for
the (unseen) stimuli presented to the blind field
was indirectly assessed by measuring RT to bilateral
versus unilateral stimuli presented to the intact
hemifield. Chronic hemian- opic patients were tested
with unilateral or bilateral black dots, both of
which could be either single or quadruple. The
latter could either have a fixed spatial
configuration repre- senting a diamond or be
randomly spatially assembled on every trial. Both
configurations covered the same extent of visual
field and had the overall same luminance. We found
that a numerosity effect as a result of increasing
the num- ber of stimuli in the blind field was
indeed present but only with the diamond
configuration. This is a convincing evi- dence that
this form of blindsight does not depend upon
stimulus numerosity per se but is likely to be
related to the presence of structured and memorized
rather than meaning- less changing stimuli.}
}
@Article{chawla.EA:99,
author = {D. Chawla and G. Rees and K. J. Friston},
title = {The physiological basis of attentional modulation in
extrastriate visual areas},
journal = NatNeuro,
year = 1999,
volume = 2,
number = 7,
pages = {671--676},
abstract = {Selective attention to color or motion enhances
activity in specialized areas of extrastriate
cortex, but mechanisms of attentional modulation
remain unclear. By dissociating modulation of
visually evoked transient activity from the baseline
for a particular attentional set, human functional
neuroimaging was used to investigate the
physiological basis of such effects. Baseline
activity in motion- and color-sensitive areas of
extrastriate cortex was enhanced by selective
attention to these attributes, even without moving
or colored stimuli. Further, visually evoked
responses increased along with baseline
activity. These results are consistent with the
hypothesis that attention modulates sensitivity of
neuronal populations to inputs by changing
background activity.}
}
@Article{chen.cave:13,
author = {Zhe Chen and Kyle R. Cave},
title = {Perceptual load vs. dilution: the roles of
attentional focus, stimulus category, and target
predictability},
journal = FP,
year = 2013,
volume = 4,
pages = 327,
abstract = {Many studies have shown that increasing the number
of neutral stimuli in a display decreases distractor
interference. This result has been interpreted
within two different frameworks; a perceptual load
account, based on a reduction in spare resources,
and a dilution account, based on a degradation in
distractor representation and/or an increase in
crosstalk between the distractor and the neutral
stimuli that contain visually similar features. In
four experiments, we systematically manipulated the
extent of attentional focus, stimulus category, and
preknowledge of the target to examine how these
factors would interact with the display set size to
influence the degree of distractor processing.
Display set size did not affect the degree of
distractor processing in all situations. Increasing
the number of neutral items decreased distractor
processing only when a task induced a broad
attentional focus that included the neutral stimuli,
when the neutral stimuli were in the same category
as the target and distractor, and when the
preknowledge of the target was insufficient to guide
attention to the target efficiently. These results
suggest that the effect of neutral stimuli on the
degree of distractor processing is more complex than
previously assumed. They provide new insight into
the competitive interactions between bottom-up and
top-down processes that govern the efficiency of
visual selective attention. }
}
@Article{clapp.gazzaley:12,
author = {Wesley C. Clapp and Adam Gazzaley},
title = {Distinct mechanisms for the impact of distraction
and interruption on working memory in aging},
journal = {Neurobiology of Aging},
year = 2012,
volume = 33,
pages = {134--148},
abstract = {Interference is known to negatively impact the
ability to maintain information in working memory
(WM), an effect that is exacerbated with
aging. Here, we explore how distinct sources of
interference, i.e., distraction (stimuli
to-be-ignored) and interruption (stimuli requiring
attention), differentially influence WM in younger
and older adults. EEG was recorded while
participants engaged in three versions of a delayed-
recognition task: no interference, a distracting
stimulus, and an interrupting stimulus presented
during WM maintenance. Behaviorally, both types of
interference negatively impacted WM accuracy in
older adults significantly more than younger adults
(with a larger deficit for interruptions). N170
latency measures revealed that the degree of
processing both distractors and interruptors
predicted WM accuracy in both populations. However,
while WM impairments could be explained by excessive
attention to distractors by older adults (a
suppression deficit), impairment induced by
interruption were not clearly mediated by
age-related increases in attention to
interruptors. These results suggest that distinct
underlying mechanisms mediate the impact of
different types of external interference on WM in
normal aging.}
}
@Article{cocchi.EA:11,
author = {Luca Cocchi and Ulrike Toepel and Marzia {De Lucia}
and Roberto Martuzzi and Stephen J. Wood and Olivia
Carter and Micah M. Murray},
title = {Working memory load improves early stages of
independent visual processing},
journal = {Neuropsychologia},
year = 2011,
volume = 49,
number = 1,
pages = {92--102},
abstract = {Increasing evidence suggests that working memory and
perceptual processes are dynamically interrelated
due to modulating activity in overlapping brain
networks. However, the direct influence of working
memory on the spatio-temporal brain dynamics of
behaviorally relevant intervening information
remains unclear. To investigate this issue, subjects
performed a visual proximity grid perception task
under three different visual--spatial working memory
(VSWM) load conditions. VSWM load was manipulated by
asking subjects to memorize the spatial locations of
6 or 3 disks. The grid was always presented between
the encoding and recognition of the disk pattern. As
a baseline condition, grid stimuli were presented
without a VSWM context. VSWM load altered both
perceptual performance and neural networks active
during intervening grid encoding. Participants
performed faster and more accurately on a
challenging perceptual task under high VSWM load as
compared to the low load and the baseline
condition. Visual evoked potential (VEP) analyses
identified changes in the configuration of the
underlying sources in one particular period
occurring 160--190 ms post-stimulus onset. Source
analyses further showed an occipito-parietal
down-regulation concurrent to the increased
involvement of temporal and frontal resources in the
high VSWM context. Together, these data suggest that
cognitive control mechanisms supporting working
memory may selectively enhance concurrent visual
processing related to an independent goal. More
broadly, our findings are in line with theoretical
models implicating the engagement of frontal regions
in synchronizing and optimizing mnemonic and
perceptual resources towards multiple goals.}
}
@Article{corballis:09correx,
author = {Michael C. Corballis},
title = {Comparing a single case with a control sample:
Correction and further comment},
journal = {Neuropsychologia},
year = 2009,
volume = 47,
number = 13,
pages = {2696--2697},
abstract = {Crawford, Garthwaite and Howell [Crawford, J. R.,
Garthwaite, P. H., & Howell, D. C. On comparing a
single case with a control sample: An alternative
perspective. Neuropsychologia, in press] correctly
point out that the t-test I suggested for asking
whether a single case belongs in the population from
which a control sample is drawn is incorrect. In
fact, the corrected formula can be interpreted
either as addressing this question, or as asking
whether the single case and the control sample are
drawn from populations with the same mean. Extension
to analysis of variance is recommended for factorial
experiments, where single case and control sample
are tested under different experimental
conditions. It is not recommended for studies in
which different tests are administered and treated
as different levels of the same dependent variable,
as in tests for neuropsychological dissociations.}
}
@Article{corballis:09,
author = {Michael C. Corballis},
title = {Comparing a single case with a control sample:
Correction and further comment},
journal = {Neuropsychologia},
year = 2009,
volume = 47,
number = 13,
pages = {2687--2689},
abstract = {Crawford and Garthwaite [Crawford, J. R. &
Garthwaite, P. H. (2002). Investigation of the
single case in neuropsychology: Confidence limits on
the abnormality and test score
differences. Neuropsychologia, 40, 1196–1208] have
proposed an adjusted t-test, widely used in
experimental neuropsychology, for comparing a single
case with a control sample. This test does not
assess whether the single-case score belongs in the
population from which the control sample is drawn,
but rather whether the mean of the distribution from
which the case was drawn differs significantly from
the mean of the control population. This approach is
readily extended to more complex designs in which
the analysis of variance is appropriate, and the
single case is treated as belonging to a group of
size one. The main qualification in using either
this or Crawford and Howell's approach is that it
makes the untestable assumption of homogeneity of
variance between the two populations, but a simple
adjustment either to the t-test or to the analysis
of variance allows one to draw conclusions about the
relation of the case itself to the control
population.}
}
@Article{cox.savoy:03,
author = {David D Cox and Robert L Savoy},
title = {Functional magnetic resonance imaging ({fMRI})
``brain reading'': detecting and classifying
distributed patterns of fMRI activity in human
visual cortex},
journal = NI,
year = 2003,
volume = 19,
number = 2,
pages = {261--270},
abstract = {Traditional (univariate) analysis of functional MRI
(fMRI) data relies exclusively on the information
contained in the time course of individual
voxels. Multivariate analyses can take advantage of
the information contained in activity patterns
across space, from multiple voxels. Such analyses
have the potential to greatly expand the amount of
information extracted from fMRI data sets. In the
present study, multivariate statistical pattern
recognition methods, including linear discriminant
analysis and support vector machines, were used to
classify patterns of fMRI activation evoked by the
visual presentation of various categories of
objects. Classifiers were trained using data from
voxels in predefined regions of interest during a
subset of trials for each subject
individually. Classification of subsequently
collected fMRI data was attempted according to the
similarity of activation patterns to prior training
examples. Classification was done using only small
amounts of data (20 s worth) at a time, so such a
technique could, in principle, be used to extract
information about a subject’s percept on a near
real-time basis. Classifiers trained on data
acquired during one session were equally accurate in
classifying data collected within the same session
and across sessions separated by more than a week,
in the same subject. Although the highest
classification accuracies were obtained using
patterns of activity including lower visual areas as
input, classification accuracies well above chance
were achieved using regions of interest restricted
to higher-order object-selective visual areas. In
contrast to typical fMRI data analysis, in which
hours of data across many subjects are averaged to
reveal slight differences in activation, the use of
pattern recognition methods allows a subtle 10-way
discrimination to be performed on an essentially
trial-by-trial basis within individuals,
demonstrating that fMRI data contain far more
information than is typically appreciated.}
}
@Article{crawford.EA:03dissoc,
author = {John R. Crawford and Paul H. Garthwaite and Colin
D. Gray},
title = {Wanted: fully operational definitions of
dissociations in single--case studies},
journal = {Cortex},
year = 2003,
volume = 39,
pages = {357--370},
abstract = {In contrast to the careful consideration given to
the issue of what we can infer from dissociations in
single-case studies, the more basic question of how
we decide whether a dissociation is present has been
relatively neglected. Proposals are made for fully
operational definitions of a deficit, classical and
strong dissociations, and double dissociations. In
developing these definitions it was assumed that
they should be based on the use of inferential
rather than descriptive statistical methods. The
scope of these definitions is limited to typical
single-case studies in which patients are compared
to control samples of a modest size. The operational
definition of a classical dissociation incorporates
a requirement that a patient’s performance on Task X
is significantly different from Task Y, in addition
to the “standard” requirement that the patient has a
deficit on Task X and is within normal limits on
Task Y. We ran a simulation to estimate the Type I
error rates when the criteria for dissociations are
applied and found these to be low (Type I errors
were defined as identifying an individual from the
control population as having a dissociation). The
inferential methods for testing whether the various
criteria are met make use of t-distributions. These
methods are contrasted with the widespread use of z
to test for a deficit or a difference between
tasks. In the latter approach the statistics of the
control sample are treated as parameters; this is
not appropriate when, as is normally the case, the
control sample size is modest in size.}
}
@Article{crawford.EA:03,
author = {John R. Crawford and Paul H. Garthwaite and David
C. Howell and Annalena Venneri},
title = {Intra-individual measures of association in
neuropsychology: Inferential methods for comparing a
single case with a control or normative sample},
journal = JINS,
year = 2003,
volume = 9,
pages = {989-1000},
abstract = {Performance on some neuropsychological tests is best
expressed as an intra-individual measure of
association (such as a parametric or non-parametric
correlation coefficient or the slope of a regression
line). Examples of the use of intra-individual
measures of association (IIMAs) include the
quantification of performance on tests designed to
assess temporal order memory or the accuracy of time
estimation. The present paper presents methods for
comparing a patient’s performance with a control or
normative sample when performance is expressed as an
IIMA. The methods test if there is a significant
difference between a patient’s IIMA and those
obtained from controls, yield an estimate of the
abnormality of the patient’s IIMA, and provide
confidence limits on the level of abnormality. The
methods can be used with normative or control
samples of any size and will therefore be of
particular relevance to single-case researchers. A
method for comparing the difference between a
patient’s scores on two measures with the
differences observed in controls is also described
(one or both measures can be IIMAs). All the methods
require only summary statistics (rather than the raw
data from the normative or control sample); it is
hoped that this feature will encourage the
development of norms for tasks that use IIMAs to
quantify performance. Worked examples of the
statistical methods are provided using data from a
clinical case and controls. A computer program (for
PCs) that implements the methods is described and
made available.}
}
@Article{crawford.garthwaite:05,
author = {John R. Crawford and Paul H. Garthwaite},
title = {Testing for Suspected Impairments and Dissociations
in Single-Case Studies in Neuropsychology:
Evaluation of Alternatives Using {Monte Carlo}
Simulations and Revised Tests for Dissociations},
journal = Neuropsychology,
year = 2005,
volume = 19,
number = 3,
pages = {318--331},
abstract = {In neuropsychological single-case studies, a patient
is compared with a small control sample. Methods of
testing for a deficit on Task X, or a significant
difference between Tasks X and Y, either treat the
control sample statistics as parameters (using z and
zD) or use modified t tests. Monte Carlo simulations
demonstrated that if z is used to test for a
deficit, the Type I error rate is high for small
control samples, whereas control of the error rate
is essentially perfect for a modified t
test. Simulations on tests for differences revealed
that error rates were very high for zD. A new method
of testing for a difference (the revised
standardized difference test) achieved good control
of the error rate, even with very small sample
sizes. A computer program that implements this new
test (and applies criteria to test for classical and
strong dissociations) is made available.}
}
@Article{crawford.garthwaite:07,
author = {John R. Crawford and Paul H. Garthwaite},
title = {Comparison of a single case to a control or
normative sample in neuropsychology: Development of
a {Bayesian} approach},
journal = CogNeuropsych,
year = 2007,
volume = 24,
number = 4,
pages = {343--372},
abstract = {Frequentist methods are available for comparison of
a patient’s test score (or score difference) to a
control or normative sample; these methods also
provide a point estimate of the percentage of the
population that would obtain a more extreme score
(or score difference) and, for some problems, an
accompanying interval estimate (i.e., confidence
limits) on this percentage. In the present paper we
develop a Bayesian approach to these
problems. Despite the very different approaches, the
Bayesian and frequentist methods yield equivalent
point and interval estimates when (a) a case’s score
is compared to that of a control sample, and (b)
when the raw (i.e., unstandardized) difference
between a case’s scores on two tasks are compared to
the differences in controls. In contrast, the two
approaches differ with regard to point estimates of
the abnormality of the difference between a case’s
standardized scores. The Bayesian method for
standardized differences has the advantages that (a)
it can directly evaluate the probability that a
control will obtain a more extreme difference score,
(b) it appropriately incorporates error in
estimating the standard deviations of the tasks from
which the patient’s difference score is derived, and
(c) it provides a credible interval for the
abnormality of the difference between an
individual’s standardized scores; this latter
problem has failed to succumb to frequentist
methods. Computer programs that implement the
Bayesian methods are described and made available.}
}
@Article{crawford.EA:09,
author = {John R. Crawford and Paul H. Garthwaite and David
C. Howell},
title = {On comparing a single case with a control sample: An
alternative perspective},
journal = {Neuropsychologia},
year = 2009,
volume = 47,
number = 13,
pages = {2690--2695},
abstract = {Corballis [Corballis, M. C. (2009). Comparing a
single case with a control sample: Refinements and
extensions. Neuropsychologia] offers an interesting
position paper on statistical inference in
single-case studies. The following points arise: (1)
Testing whether we can reject the null hypothesis
that a patient's score is an observation from the
population of control scores can be a legitimate aim
for single-case researchers, not just
clinicians. (2) Counter to the claim made by
Corballis [Corballis, M. C. (2009). Comparing a
single case with a control sample: Refinements and
extensions. Neuropsychologia], Crawford and Howell's
[Crawford, J. R., & Howell, D. C. (1998). Comparing
an individual's test score against norms derived
from small samples. The Clinical Neuropsychologist,
12, 482–486] method does test whether we can reject
the above null hypothesis. (3) In all but the most
unusual of circumstances Crawford and Howell's
method can also safely be used to test whether the
mean of a notional patient population is lower than
that of a control population, should
neuropsychologists wish to construe the test in this
way. (4) In contrast, the method proposed by
Corballis is not legitimate for either of these
purposes because it fails to allow for uncertainty
over the control mean (as a result Type I errors
will not be under control). (5) The use of a mixed
ANOVA design to compare a case to controls (with or
without the adjustment proposed by Corballis) is
beset with problems but these can be overcome using
alternative methods.}
}
@Article{crawford.EA:10,
author = {John R. Crawford and Paul H. Garthwaite and Sara
Porter},
title = {Point and interval estimates of effect sizes for the
case-controls design in neuropsychology: Rationale,
methods, implementations, and proposed reporting
standards},
journal = CogNeuropsych,
year = 2010,
volume = 27,
number = 3,
pages = {245--260},
abstract = {It is increasingly common for group studies in
neuropsychology to report effect sizes. In contrast
this is rarely done in single-case studies (at least
in those studies that employ a case-controls
design). The present paper sets out the advantages
of reporting effect sizes, derives suitable effect
size indexes for use in single-case studies, and
develops methods of supplementing point estimates of
effect sizes with interval estimates. Computer
programs that implement existing classical and
Bayesian inferential methods for the single case (as
developed by Crawford, Garthwaite, Howell, and col-
leagues) are upgraded to provide these point and
interval estimates. The upgraded programs can be
downloaded from
www.abdn.ac.uk/~psy086/dept/Single_Case_Effect_Sizes.htm}
}
@Article{crawford.EA:11,
author = {John R. Crawford and Paul H. Garthwaite and Kevin
Ryan},
title = {Comparing a single case to a control sample: Testing
for neuropsychological deficits and dissociations in
the presence of covariates},
journal = {Cortex},
year = 2011,
volume = 47,
pages = {1166--1178},
abstract = {Existing inferential methods of testing for a
deficit or dissociation in the single case are
extended to allow researchers to control for the
effects of covariates. The new (Bayesian) methods
provide a significance test, point and interval
estimates of the effect size for the difference
between the case and controls, and point and
interval estimates of the abnor- mality of a case’s
score, or standardized score difference. The methods
have a wide range of potential applications, e.g.,
they can provide a means of increasing the
statistical power to detect deficits or
dissociations, or can be used to test whether
differences between a case and controls survive
partialling out the effects of potential confounding
variables. The methods are implemented in a series
of computer programs for PCs (these can be down-
loaded from
www.abdn.ac.uk/wpsy086/dept/Single_Case_Covariates.htm). Illustrative
examples of the methods are provided.}
}
@article{crinion.EA:07,
author = {Jenny Crinion and John Ashburner and Alex Leff and
Matthew Brett and Cathy Price and Karl Friston},
title = {Spatial normalization of lesioned brains:
Performance evaluation and impact on {fMRI}
analyses},
journal = NI,
year = 2007,
volume = 37,
number = 3,
pages = {866--875},
abstract = {A key component of group analyses of neuroimaging
data is precise and valid spatial normalization
(i.e., inter-subject image registration). When
patients have structural brain lesions, such as a
stroke, this process can be confounded by the lack
of correspondence between the subject and
standardized template images. Current procedures for
dealing with this problem include regularizing the
estimate of warping parameters used to match
lesioned brains to the template, or “cost function
masking”; both these solutions have significant
drawbacks. We report three experiments that identify
the best spatial normalization for structurally
damaged brains and establish whether differences
among normalizations have a significant effect on
inferences about functional activations. Our novel
protocols evaluate the effects of different
normalization solutions and can be applied easily to
any neuroimaging study. This has important
implications for users of both structural and
functional imaging techniques in the study of
patients with structural brain damage.}
}
@Article{danckert.EA:03,
author = {James Danckert and Patrice Revol and Laure Pisella
and Pierre Krolak-Salmon and Alain Vighetto and
Melvyn A. Goodale and Yves Rossetti},
title = {Measuring unconscious actions in action-blindsight:
exploring the kinematics of pointing movements to
targets in the blind field of two patients with
cortical hemianopia},
journal = {Neuropsychologia},
year = 2003,
volume = 41,
pages = {1068--1081},
abstract = { We tested two patients with posterior cerebral
lesions on two pointing tasks. In the first task,
the patients pointed to targets presented on a touch
screen monitor and pointing accuracy was
recorded. One patient (JR) demonstrated good
localisation of targets presented to her blind field
while the other patient (YP) did not. Movement
kinematics were measured in the second task to
compare the kinematics of movements made to sighted
field targets with those made to blind field
targets. For this version of the task both patients
demonstrated above chance localisation of blind
field targets although the slope of the relationship
between the end of pointing movements and the target
locations was significantly steeper for JR than for
YP. Furthermore, JR showed a kinematic profile for
movements made to blind field targets that mirrored
the profile of kinematics to sighted field
targets. That is, both peak velocity and time to
peak velocity increased with increasing target
eccentricity for movements made to blind and sighted
field targets alike. Although patient YP now showed
more reliable spatial localisation on this pointing
task when compared with the touch screen task, his
kinematics for movements made to targets in his
blind field were quite different from those made to
targets in his sighted field. Based on the patients’
CT scans, we suggest that the superior performance
of patient JR is a consequence of greater sparing of
her parietal cortex in the damaged hemisphere.}
}
@Article{danckert.rossetti:05,
author = {James Danckert and Yves Rossetti},
title = {Blindsight in action: what can the different
sub-types of blindsight tell us about the control of
visually guided actions?},
journal = NBR,
year = 2005,
volume = 29,
number = 7,
pages = {1035--1046},
abstract = {Blindsight broadly refers to the paradoxical
neurological condition where patients with a visual
field defect due to a cortical lesion nevertheless
demonstrate implicit residual visual sensitivity
within their field cut. The aim of this paper is
twofold. First, through a selective review of the
blindsight literature we propose a new taxonomy for
the subtypes of residual abilities described in
blindsight. Those patients able to accurately act
upon blind field stimuli (e.g. by pointing or
saccading towards them) are classified as having
‘action-blindsight’, those whose residual functions
can be said to rely to some extent upon attentive
processing of blind field stimuli are classified as
demonstrating ‘attention-blindsight’, while finally,
patients who have somewhat accurate perceptual
judgements for blind field stimuli despite a
complete lack of any conscious percept, are
classified as having ‘agnosopsia’—literally meaning
‘not knowing what one sees’. We also address the
possible neurological substrates of these residual
sensory processes. Our second aim was to
investigate the most striking subtype of blindsight,
action-blindsight. We review the data relevant to
this subtype and the hypotheses proposed to account
for it, before speculating on how action-blindsight
may inform our normal models of visuomotor control.}
}
@InCollection{danckert.mirsattarri:12,
author = {James Danckert and Seyed M. Mirsattarri},
title = {Neuroimaging of Single Cases: Benefits and Pitfalls},
booktitle = {Neuroimaging -- Cognitive and Clinical Neuroscience},
publisher = {InTech},
year = 2012,
editor = {Peter Bright},
note = {doi: 10.5772/22983}
}
@InCollection{dirusso.EA:02,
author = {Francesco {Di Russo} and Wolfgang
A. Teder-S{\"a}̈llej{\"a}rvi and Steven A. Hillyard},
title = {{Steady-State VEP} and Attentional Visual
Processing},
booktitle = {The Cognitive Electrophysiology of Mind and Brain},
publisher = {Academic Press},
year = 2002,
editor = {Alberto Zani and Alice Mado Proverbio},
pages = {259--274},
address = {Amsterdam},
abstract = {The vast majority of studies that investi- gated
attentional modulation of the visual evoked
potential (VEP) have been confined to the transient
responses evoked by iso- lated stimuli. This class
of potentials is evoked by stimuli having an
asynchronous and low repetition rate (not faster
than 2 stimuli per second). These potentials are
called “transient” because the slow rate of
stimulation allows the sensory pathways to recover
or “reset” before the next stimulus appears. When
visual stimuli are presented at a constant rate that
is rapid enough to prevent the evoked neural
activity from returning to base line state, the
elicited response becomes continuous and is called
the steady-state visual evoked potential
(SSVEP). With steady-state stimulation the typical
VEP wave form is markedly changed. For instance, the
transient VEP includes three major early components:
the C1 at 60–80 msec, the P1 at 80–120 msec, and the
N1 at 120–180 msec. (see Fig. 1). At more rapid
stimulation rates, the brain response to the same
stimulus becomes sinusoidal and is typically
modulated at the fundamental stimulus frequency in
the case of an unstructured stimulus (e.g. flash) or
at the second harmonic (double the stimulation
frequency) if the stimulus is a pattern-reversal
(Regan, 1989). Like any sinusoidal wave form, the
SSVEP can be measured in terms of its amplitude and
phase. The phase is a joint function of the stimulus
frequency and the time delay between stimulus and
brain response. The amplitude indicates the rela-
tive magnitude of a given harmonic of the response
and, as for transient evoked potentials, is measured
in microvolts. The amplitude and phase of the SSVEP
vary as function of the temporal frequency, spatial
frequency, contrast, luminance, and hue of the
driving stimulus (Regan, 1989).}
}
@Article{dilks.EA:07,
author = {Daniel D. Dilks and John T. Serences and Benjamin
J. Rosenau and Steven Yantis and Michael McCloskey},
title = {Human adult cortical reorganization and consequent
visual distortion},
journal = JoN,
year = 2007,
volume = 27,
number = 36,
pages = {9585--9594},
abstract = {Neural and behavioral evidence for cortical
reorganization in the adult somatosensory system
after loss of sensory input (e.g., amputation) has
been well documented. In contrast, evidence for
reorganization in the adult visual system is far
less clear: neural evidence is the subject of
controversy, behavioral evidence is sparse, and
studies combining neural and behavioral evidence
have not previously been reported. Here, we report
converging behavioral and neuroimaging evidence from
a stroke patient (B.L.) in support of cortical
reorganization in the adult human visual
system. B.L.'s stroke spared the primary visual
cortex (V1), but destroyed fibers that normally
provide input to V1 from the upper left visual field
(LVF). As a consequence, B.L. is blind in the upper
LVF, and exhibits distorted perception in the lower
LVF: stimuli appear vertically elongated, toward and
into the blind upper LVF. For example, a square
presented in the lower LVF is perceived as a
rectangle extending upward. We hypothesized that the
perceptual distortion was a consequence of cortical
reorganization in V1. Extensive behavioral testing
supported our hypothesis, and functional magnetic
resonance imaging (fMRI) confirmed V1
reorganization. Together, the behavioral and fMRI
data show that loss of input to V1 after a stroke
leads to cortical reorganization in the adult human
visual system, and provide the first evidence that
reorganization of the adult visual system affects
visual perception. These findings contribute to our
understanding of the human adult brain's capacity to
change and has implications for topics ranging from
learning to recovery from brain damage.}
}
@Article{dirusso.EA:03,
author = {Francesco {Di Russo} and Antigona Mart{\'i}nez and
Steven A. Hillyard},
title = {Source Analysis of Event-related Cortical Activity
during Visuo-spatial Attention},
journal = CC,
year = 2003,
volume = 13,
pages = {486--499},
abstract = {Recordings of event-related potentials (ERPs) were
combined with structural and functional magnetic
resonance imaging (fMRI) to study the
spatio-temporal patterns of cortical activity that
underlie visual–spatial attention. Small
checkerboard stimuli were flashed in random order to
the four quadrants of the visual field at a rapid
rate while subjects attended to stimuli in one
quadrant at a time. Attended stimuli elicited
enhanced ERP components in the latency range 80–200
ms that were co-localized with fMRI activations in
multiple extrastriate cortical regions. The earliest
ERP component (C1 at 50–90 ms) was unaffected by
attention and was localized by dipole modeling to
calcarine cortex. A longer latency deflection in the
150–225 ms range that was accounted for by this same
calcarine source, however, did show consistent
modulation with attention. This late attention
effect, like the C1, inverted in polarity for upper
versus lower field stimuli, consistent with a neural
generator in primary visual cortex (area V1). These
results provide support to current hypotheses that
spatial attention in humans is associated with
delayed feedback to area V1 from higher extrastriate
areas that may have the function of improving the
salience of stimuli at attended locations.}
}
@Article{dirusso.EA:07,
author = {Francesco {Di Russo} and Sabrina Pitzalis and Teresa
Aprile and Grazia Spitoni and Fabiana Patria and
Alessandra Stella and Donatella Spinelli and Steven
A. Hillyard},
title = {Spatiotemporal analysis of the cortical sources of
the steady-state visual evoked potential},
journal = HBM,
year = 2007,
volume = 28,
number = 4,
pages = {323--334},
abstract = {This study aimed to characterize the neural
generators of the steady-state visual evoked
potential (SSVEP) to repetitive, 6 Hz
pattern-reversal stimulation. Multichannel scalp
recordings of SSVEPs and dipole modeling techniques
were combined with functional magnetic resonance
imaging (fMRI) and retinotopic mapping in order to
estimate the locations of the cortical sources
giving rise to the SSVEP elicited by pattern
reversal. The time-varying SSVEP scalp topography
indicated contributions from two major cortical
sources, which were localized in the medial
occipital and mid-temporal regions of the
contralateral hemisphere. Colocalization of dipole
locations with fMRI activation sites indicated that
these two major sources of the SSVEP were located in
primary visual cortex (V1) and in the motion
sensitive (MT/V5) areas, respectively. Minor
contributions from mid-occipital (V3A) and ventral
occipital (V4/V8) areas were also
considered. Comparison of SSVEP phase information
with timing information collected in a previous
transient VEP study (Di Russo et al. [2005]
Neuroimage 24:874-886) suggested that the sequence
of cortical activation is similar for steady-state
and transient stimulation. These results provide a
detailed spatiotemporal profile of the cortical
origins of the SSVEP, which should enhance its use
as an efficient clinical tool for evaluating
visual-cortical dysfunction as well as an
investigative probe of the cortical mechanisms of
visual-perceptual processing.}
}
@Article{dirusso.EA:12,
author = {Francesco {Di Russo} and Alessandra Stella and
Grazia Spitoni and Francesca Strappini and Stefano
Sdoia and Gaspare Galati and Steven A. Hillyard and
Donatella Spinelli and Sabrina Pitzalis},
title = {Spatiotemporal Brain Mapping of Spatial Attention
Effects on Pattern-Reversal {ERPs}},
journal = HBM,
year = 2012,
volume = 33,
pages = {1334--1351},
abstract = {Recordings of event-related potentials (ERPs) were
combined with structural and functional magnetic
resonance imaging (fMRI) to investigate the timing
and localization of stimulus selection processes
during visual-spatial attention to pattern-reversing
gratings. Pattern reversals were presented in random
order to the left and right visual fields at a rapid
rate, while subjects attended to the rever- sals in
one field at a time. On separate runs, stimuli were
presented in the upper and lower visual
quadrants. The earliest ERP component (C1, peaking
at around 80 ms), which inverted in polarity for
upper versus lower field stimuli and was localized
in or near visual area V1, was not modulated by
attention. In the latency range 80–250 ms, multiple
components were elicited that were increased in
amplitude by attention and were colocalized with
fMRI activations in specific visual cortical
areas. The principal anatomical sources of these
attention-sensitive components were localized by
fMRI-seeded dipole modeling as follows: P1 (ca. 100
ms—source in motion-sensitive area MTþ), C2 (ca. 130
ms— same source as C1), N1a (ca. 145 ms—source in
horizontal intraparietal sulcus), N1b (ca. 165 ms—
source in fusiform gyrus, area V4/V8), N1c (ca. 180
ms—source in posterior intraparietal sulcus, area
V3A), and P2 (ca. 220 ms—multiple sources, including
parieto-occipital sulcus, area V6). These results
support the hypothesis that spatial attention acts
to amplify both feed-forward and feedback signals in
multiple visual areas of both the dorsal and ventral
streams of processing.}
}
@Article{dirusso.EA:16,
author = {Francesco {Di Russo} and Giuliana Lucci and
Valentina Sulpizio and Marika Berchicci and
Donatella Spinelli and Sabrina Pitzalis and Gaspare
Galati},
title = {Spatiotemporal brain mapping during preparation,
perception, and action},
journal = NI,
year = 2016,
volume = 126,
pages = {1--14},
abstract = {Deciding whether to act or not to act is a
fundamental cognitive function. To avoid incorrect
responses, both re- active and proactive modes of
control have been postulated. Little is known,
however, regarding the brain imple- mentation of
proactive mechanisms, which are deployed prior to an
actual need to inhibit a response. Via a combination
of electrophysiological and neuroimaging measures
(recorded in 21 and 16 participants, respective-
ly), we describe the brain localization and timing
of neural activity that underlies the anticipatory
proactive mechanism. From these results, we conclude
that proactive control originates in the inferior
Frontal gyrus, is established well before stimulus
perception, and is released concomitantly with
stimulus appearance. Stimulus perception triggers
early activity in the anterior insula and
intraparietal cortex contralateral to the responding
hand; these areas likely mediate the transition from
perception to action. The neural activities leading
to the de- cision to act or not to act are described
in the framework of a three-stage model that
includes perception, action, and anticipatory
functions taking place well before stimulus onset.}
}
@Article{driver.mattingley:98,
author = {Jon Driver and Jason B. Mattingley},
title = {Parietal neglect and visual awareness},
journal = NatNeuro,
year = 1998,
volume = 1,
pages = {17--22},
abstract = {The last decade has seen a resurgence of interest in
the neural correlates of conscious vision, with most
discussion focused on the 'blindsight' that can
follow damage to primary visual cortex, in the
occipital lobe. We suggest that new insights into
the neural basis of visual awareness may be gleaned
from a different neuropsychological phenomenon,
namely visual 'neglect' after injury to regions in
the parietal lobe. Neglect provides several
revealing contrasts with occipital blindsight. Here
we summarise four key findings. First, unlike the
deficits caused by damage to primary visual cortex,
the loss of awareness in parietal neglect is
characteristically not strictly retinotopic. Second,
visual segmentation processes are preserved in
neglect, and can influence what will reach the
patient's awareness. Third, extensive unconscious
processing takes place for those stimuli on the
neglected side which escape awareness, including
some degree of object identification. Finally,
parietal damage affects initial stages of motor
planning as well as perception. These findings are
consistent with recent data on single-cell activity
in the monkey brain. They also suggest why areas in
the inferior parietal lobe may play a prominent role
in visual awareness.}
}
@Article{eklund.EA:12,
author = {Anders Eklund and Mats Andersson and Camilla
Josephson and Magnus Johannesson and Hans Knutsson},
title = {Does parametric {fMRI} analysis with {SPM} yield
valid results? -- An empirical study of 1484 rest
datasets},
journal = NI,
year = 2012,
volume = 61,
number = 3,
pages = {565--578},
abstract = {The validity of parametric functional magnetic
resonance imaging (fMRI) analysis has only been
reported for simulated data. Recent advances in
computer science and data sharing make it possible
to analyze large amounts of real fMRI data. In this
study, 1484 rest datasets have been analyzed in
SPM8, to estimate true familywise error rates. For a
familywise significance threshold of 5\%, significant
activity was found in 1\%–70\% of the 1484 rest
datasets, depending on repetition time, paradigm and
parameter settings. This means that parametric
significance thresholds in SPM both can be
conservative or very liberal. The main reason for
the high familywise error rates seems to be that the
global AR(1) auto correlation correction in SPM
fails to model the spectra of the residuals,
especially for short repetition times. The findings
that are reported in this study cannot be
generalized to parametric fMRI analysis in general,
other software packages may give different
results. By using the computational power of the
graphics processing unit (GPU), the 1484 rest
datasets were also analyzed with a random
permutation test. Significant activity was then
found in 1\%–19\% of the datasets. These findings
speak to the need for a better model of temporal
correlations in fMRI timeseries.}
}
@InProceedings{eklund.EA:15,
author = {Anders Eklund and Thomas Nichols and Mats Andersson
and Hans Knutsson},
title = {Empirically investigating the statistical validity
of {SPM, FSL and AFNI} for single subject {fMRI}
analysis},
booktitle = {IEEE 12th International Symposium on Biomedical
Imaging (ISBI)},
year = 2015,
pages = {1376--1380},
organization = {IEEE},
abstract = {The software packages SPM, FSL and AFNI are the most
widely used packages for the analysis of functional
magnetic resonance imaging (fMRI) data. Despite this
fact, the validity of the statistical methods has
only been tested using simulated data. By analyzing
resting state fMRI data (which should not contain
specific forms of brain activity) from 396 healthy
con- trols, we here show that all three software
packages give in- flated false positive rates
(4\%--96\% compared to the expected 5\%). We isolate
the sources of these problems and find that SPM
mainly suffers from a too simple noise model, while
FSL underestimates the spatial smoothness. These
results highlight the need of validating the
statistical methods being used for fMRI.}
}
@Article{ellis.EA:06,
author = {Kathryn A. Ellis and Richard B. Silberstein and
Pradeep J. Nathan},
title = {Exploring the temporal dynamics of the spatial
working memory n-back task using steady state visual
evoked potentials {(SSVEP)}},
journal = NI,
year = 2006,
volume = 31,
pages = {1741--1751},
abstract = {The neural networks associated with spatial working
memory (SWM) are well established. However, the
temporal dynamics of SWM-related brain activity are
less clear. This study examined changes in temporal
neurophysiology during the spatial n-back task using
steady state probe topography (SSPT) to record
cortical steady state visual evoked potentials
(SSVEPs) at 64 scalp locations. Twenty healthy male
volunteers participated in the study. The findings
identified three different time periods of
significance during the spatial n-back task— an
early perceptual/encoding period (approximately
0–500 ms), an early delay period just following the
stimulus disappearing from view (approximately 850 –
1400 ms), and a late period lasting the final second
of the delay and anticipation of the new stimulus
(approxi- mately 2500 – 3500 ms). The delay period
was associated with increases in frontal and
occipital region amplitude, consistent with previous
findings in more basic working memory tasks. The two
different SSVEP components during the delay appear
reflective of the additional ‘‘executive’’ demands
associated with the n-back and may suggest variable
roles for the PFC during different stages of the
delay. All three n-back levels demonstrated a
relative consistent electrophysiological profile,
indicating that this pattern is specific to the
spatial n-back task. Nevertheless, these findings
supported the hypothesis that memory load modulates
activity within the networks identified, consistent
with previous neuroimaging studies. The current
findings may offer a framework in which to further
investigate the temporal aspects of SWM.}
}
@InCollection{fahle:03,
author = {Manfred Fahle},
title = {Failures of visual analysis: scotoma, agnosia, and
neglect},
booktitle = {The Neuropsychology of Vision},
publisher = {Oxford University Press},
year = 2003,
editor = {Manfred Fahle and Mark Greenlee},
pages = {179--258},
address = {Oxford},
abstract = {This chapter deals with different types of failure
to analyse the visual world, starting with the
complete loss of vision, blindness, as well as
blindness for circumscribed parts of the visual
field, scotomata. It also reports some syndromes
characterized by difficulties in perception of and
discrimination between different domains or
submodalities of vision, while leaving most others
intact, such as acquired inability to assess visual
motion, or acquired colour blindness caused by
cerebral damage (achromatopsia). It then provides an
overview of the most astonishing examples of failed
visual perception: simultanagnosia; neglect; and
Balint's syndrome. These syndromes share the
phenomenon that conscious perception of objects in
(parts of) the peripheral visual field is absent in
spite of intact stimulation of the primary visual
cortex by these objects. It also attempts to fill in
some gaps of knowledge by means of speculation to
produce a consistent taxonomy of symptoms
encountered in visual neuropsychology. It combines
the theoretical background with clinical findings
and with a description of at least some of the
methods used to diagnose patients suffering from
failures of visual analysis.}
}
@article{faulkner.foster:02,
author = {Deborah Faulkner and Jonathan Foster},
title = {The Decoupling of {"}Explicit{"}and {"}Implicit{"}
Processing in Neuropsychological Disorders: Insights
into the Neural Basis of Consciousness?},
journal = {Psyche -- An interdisciplinary journal of research
on consciousness},
year = 2002,
volume = 8,
number = 2,
abstract = {A key element of the distinction between explicit
and implicit cognitive functioning is the presence
or absence of conscious awareness. In this review,
we consider the proposal that neuropsychological
disorders can best be considered in terms of a
decoupling between preserved implicit or unconscious
processing and impaired explicit or conscious
processing. Evidence for dissociations between
implicit and explicit processes in blindsight,
amnesia, object agnosia, prosopagnosia,
hemi-neglect, and aphasia is examined. The
implications of these findings for a) our
understanding of a variety of neuropsychological
disorders, b) the conceptualization of normal
cognitive functioning, c) the neural basis of
consciousness, and d) the clinical rehabilitation of
brain-injured individuals are also discussed.}
}
@Article{fawcett.EA:04,
author = {Ian P. Fawcett and Gareth R. Barnes and Arjan
Hillebrand and Krish D. Singh},
title = {The temporal frequency tuning of human visual cortex
investigated using synthetic aperture magnetometry},
journal = NI,
year = 2004,
volume = 21,
number = 4,
pages = {1542--1555},
abstract = {Using synthetic aperture magnetometry (SAM) analyses
of magnetoencephalographic (MEG) data, we
investigated the variation in cortical response
magnitude and frequency as a function of stimulus
temporal frequency. In two separate experiments, a
reversing checkerboard stimulus was used in the
right or left lower visual field at frequencies from
0 to 21 Hz. Average temporal frequency tuning curves
were constructed for regions-of-interest located
within medial visual cortex and V5/MT. In medial
visual cortex, it was found that both the frequency
and magnitude of the steady-state response varied as
a function of the stimulus frequency, with multiple
harmonics of the stimulus frequency being found in
the response. The maximum fundamental response was
found at a stimulus frequency of 8 Hz, whilst the
maximum broadband response occurred at 4 Hz. In
contrast, the magnitude and frequency content of the
evoked onset response showed no dependency on
stimulus frequency. Whilst medial visual cortex
showed a power increase during stimulation,
extra-striate areas such as V5/MT exhibited a
bilateral event-related desynchronisation (ERD). The
frequency content of this ERD did not depend on the
stimulus frequency but was a broadband power
reduction across the 5–20 Hz frequency range. The
magnitude of this ERD within V5/MT was strongly
low-pass tuned for stimulus frequency, and showed
only a moderate preference for stimuli in the
contralateral visual field.}
}
@Article{fellrath.ptak:15,
author = {Julia Fellrath and Radek Ptak},
title = {The role of visual saliency for the allocation of
attention: Evidence from spatial neglect and
hemianopia},
journal = {Neuropsychologia},
year = 2015,
volume = 73,
pages = {70--81},
abstract = {Visual scanning and exploration of natural scenes
not only depends on specific objects, but also on
local features. Models of spatial attention propose
that features such as orientation or colour are
processed pre-attentively and in parallel. According
to these models attention interferes at a later
stage, where features are combined into a
representation of visual saliency. Saliency is a
good predictor of ocular fixations during scanning
of static pictures. Here, we tested whether
fixations of patients with left spatial neglect,
hemianopia, or both can be predicted based on local
image content. Participants were asked to freely
scan natural images while saccades and ocular
fixations were registered. Hemianopic patients
produced a similar distribution of fixations and
relied similarly on picture saliency as healthy
controls. In contrast, neglect patients looked to
image regions with increased saliency and higher
local orientation and intensity thresholds on the
neglected side of space. The reliance on increased
saliency during visual exploration was predicted by
damage to subcortical regions interconnecting the
inferior parietal and lateral premotor cortex. These
findings suggest that spatial neglect leads to a
combined attentive and pre-attentive deficit in the
processing of saliency and feature information.}
}
@Article{ffytche.zeki:11,
author = {Dominic H. Ffytche and Semir Zeki},
title = {The primary visual cortex, and feedback to it, are
not necessary for conscious vision},
journal = {Brain},
year = 2011,
volume = 134,
number = 1,
pages = {247--257},
abstract = {A compelling single case report of visual awareness
(visual qualia) without primary visual cortex would
be sufficient to refute the hypothesis that the
primary visual cortex and the back-projections to it
are necessary for conscious visual experience. In a
previous study, we emphasized the presence of crude
visual awareness in Patient G.Y., with a lesion of
the primary visual cortex, who is aware of, and able
to discriminate, fast-moving visual stimuli
presented to his blind field. The visual nature of
Patient G.Y.’s blind field experience has since been
questioned and it has been suggested that the
special circumstances of repeated testing over
decades may have altered Patient G.Y.’s visual
pathways. We therefore sought new evidence of visual
awareness without primary visual cortex in patients
for whom such considerations do not apply. Three
patients with hemianopic field defects (Patient
G.N. and Patient F.B. with MRI confirmed primary
visual cortex lesions, Patient C.G. with an inferred
lesion) underwent detailed psychophysical testing in
their blind fields. Visual stimuli were presented at
different velocities and contrasts in two- and
four-direction discrimination experiments and the
direction of motion and awareness reported using a
forced-choice paradigm. Detailed verbal reports were
also obtained of the nature of the blind field
experience with comparison of the drawings of the
stimulus presented in the blind and intact fields,
where possible. All three patients reported visual
awareness in their blind fields. Visual awareness
was significantly more likely when a moving stimulus
was present compared to no stimulus catch trials
(P < 0.01 for each subject). Psychophysical
performance in Patient F.B. and Patient G.N. was
consistent with the Riddoch syndrome, with higher
levels of visual awareness for moving compared to
static stimuli (P < 0.001) and intact direction
discrimination (P < 0.0001 for two- and
four-direction experiments). Although the blind
field experience of all three subjects was degraded,
it was clearly visual in nature. We conclude that
the primary visual cortex or back-projections to it
are not necessary for visual awareness.}
}
@Article{friston.EA:99,
author = {Karl J. Friston and Andrew P. Holmes and Keith
J. Worsley},
title = {How Many Subjects Constitute a Study?},
journal = NI,
year = 1999,
volume = 10,
pages = {1--5},
abstract = {In fMRI there are two classes of inference: one aims
to make a comment about the ‘‘typical’’
characteristics of a population, and the other about
‘‘average’’ charac- teristics. The first pertains to
studies of normal sub- jects that try to identify
some qualitative aspect of normal functional
anatomy. The second class necessar- ily applies to
clinical neuroscience studies that want to make an
inference about quantitative differences of a
regionally specific nature. The first class of
inferences is adequately serviced by conjunction
analyses and fixed-effects models with relatively
small numbers of subjects. The second requires
random-effect analyses and larger cohorts.}
}
@Article{garcia.EA:13,
author = {Javier O. Garcia and Ramesh Srinivasan and John
T. Serences},
title = {Near-Real-Time Feature-Selective Modulations in
Human Cortex},
journal = CurrBio,
year = 2013,
volume = 23,
pages = {515--522},
abstract = {For neural activity to be linked with cognitive
function, infor- mation is needed about both the
temporal dynamics and the content of neural
codes. Traditionally, recording of single neurons in
animals has been the primary means of obtaining high
temporal resolution and precise information about
neural tuning properties such as selectivity for
different sensory features. Recent functional
magnetic resonance imaging (fMRI) studies in humans
have been able to measure feature selectivity within
specific subregions of sensory cortex (e.g.,
orientation selectivity in primary visual cortex, or
V1) [1, 2]. However, investigating the neural
mechanisms that support cognitive processing—which
often occurs rapidly on a subsecond scale—with a
temporally insensitive method such as fMRI severely
limits the types of inferences that can be
drawn. Here, we describe a new method for tracking
the rapid temporal evolution of feature-selective
information processing with scalp recordings of
electroen- cephalography (EEG). We generate
orientation-selective response profiles based on the
spatially distributed pattern of steady-state visual
evoked potential (SSVEP) responses to flickering
visual stimuli. Using this approach, we report a
multiplicative attentional modulation of these
feature- selective response profiles with a temporal
resolution of 24–120 ms, which is far faster than
that achieved with fMRI. Finally, we show that
behavioral performance on a discrimi- nation task
can be predicted based on the amplitude of these
temporally precise feature-selective response
profiles. This method thus provides a
high-temporal-resolution metric that can be used to
track the influence of cognitive manipu- lations on
feature-selective information processing in human
cortex.}
}
@Article{gazzaniga:95,
author = {Michael S. Gazzaniga},
title = {Principles of Human Brain Organization Derived from
Split-Brain Studies},
journal = {Neuron},
year = 1995,
volume = 14,
pages = {217--228}}
@Article{goebel.EA:01,
author = {Rainer Goebel and Lars Muckli and Friedhelm
E. Zanella and Wolf Singer and Petra Stoerig},
title = {Sustained extrastriate cortical activation without
visual awareness revealed by {fMRI} studies of
hemianopic patients},
journal = VisRes,
year = 2001,
volume = 41,
pages = {1459--1474},
abstract = {Patients with lesions in the primary visual cortex
(V1) may show processing of visual stimuli presented
in their field of cortical blindness even when they
report being unaware of the stimuli. To elucidate
the neuroanatomical basis of their residual visual
functions, we used functional magnetic resonance
imaging in two hemianopic patients, FS and GY. In
the first experiment, a rotating spiral stimulus was
used to assess the responsiveness of dorsal stream
areas. Although no response was detectable within
denervated or destroyed early visual cortex,
motion-sensitive areas (hMT+/V5) ipsilateral to the
lesion showed a strong sustained hemodynamic
response. In GY, this activation was at least as
strong as that of his contralesional hMT+/V5 to the
stimulus in the normal hemifield. In the second
experiment, coloured images of natural objects were
used to assess the responsiveness of ventral stream
areas. Again, no activity was detectable in
ipsilesional early visual areas, but extrastriate
areas in the lateral occipital cortex (hMT+/V5 and
LO) and within the posterior fusiform gyrus (V4/V8)
showed a robust sustained hemodynamic response. In
both experiments, we observed that ipsilesional
areas responded to stimuli presented in either
hemifield, whereas the normal hemisphere responded
preferentially to stimuli in the sighted
hemifield. As only one subject occasionally noticed
the onset of stimuluation in the impaired field, the
unexpectedly strong sustained activity in
ipsilesional dorsal and ventral cortical areas
appears to be insufficient to generate conscious
vision.}
}
@Article{gonzalezortiz.EA:13,
author = {S. Gonz{\'a}lez-Ortiz and L. Oleaga and T. Pujol and
S. Medrano and J. Rumi{\'a} and L. Caral and
T. Boget and J. Capellades and N. Bargall{\'}},
title = {Simple {fMRI} Postprocessing Suffices for Normal
Clinical Practice},
journal = AJNR,
year = 2013,
volume = 34,
pages = {1188--1193},
note = {dx.doi.org/10.3174/ajnr.A3381},
abstract = {BACKGROUND AND PURPOSE: Whereas fMRI postprocessing
tools used in research are accurate but unwieldy,
those used for clinical practice are user-friendly
but are less accurate. We aimed to determine whether
commercial software for fMRI postprocessing is
accurate enough for clinical practice. METHODS: Ten
volunteers underwent fMRI while performing motor and
language tasks (hand, foot, and orolingual
movements; verbal fluency; semantic judgment; and
oral comprehension). We compared visual concordance,
image quality (noise), voxel size, and radiologist
preference for the activation maps obtained by using
Neuro3D software (provided with our MR imaging
scanner) and by using the SPM program commonly used
in research. RESULTS: Maps obtained with the 2
methods were classified as "partially overlapping"
for 70\% for motor and 72\% for language paradigm
experiments and as “overlapping” in 30\% of motor
and in 15\% of language paradigm experiments.
CONCLUSIONS: fMRI is a helpful and robust tool in
clinical practice for planning neurosurgery. Widely
available commercial fMRI software can provide
reliable information for therapeutic management, so
sophisticated, less widely available software is
unnecessary in most cases.}
}
@Article{gorgolewski.EA:12,
author = {Krzysztof J. Gorgolewski and Amos J. Storkey and
Mark E. Bastin and Ian Whittle and Cyril Pernet},
title = {Single subject {fMRI} test–retest reliability
metrics and confounding factors},
journal = NI,
year = 2012,
volume = 69,
pages = {231--243},
abstract = {For the past twenty years, the tool of choice for
non-invasive study of human mind/brain relationships
has been functional Magnetic Res- onance Imaging
(fMRI). Despite the fact that it has been used in
thou- sands of studies, many of which have been
independently replicated, there is as yet no
consensus on how reliable fMRI measurements are
(Bennett and Miller, 2010). At the same time it is
widely accepted that fMRI can provide valuable
insights into the human brain even when used on the
single subject level. In other words, the result of
analysing fMRI time-series is not random. However,
it is also accepted that there is some variability
in the results that cannot be accounted for by
experimental variables. Understanding this
variability of fMRI is crucial to delineating limits
of fMRI as a research tool. The pursuit of
scientific truth is not the only motivation behind
understanding the reliability of fMRI. Shortly after
its inception fMRI was adapted for clinical use. For
example, presurgical mapping for ⁎ Corresponding
author at: Neuroinformatics and Computational
Neuroscience, Doctoral Training Centre, School of
Informatics, University of Edinburgh, 10 Crichton
Street, Edinburgh, EH8 9AB, UK. E-mail address:
[email protected] (K.J. Gorgolewski).
1053-8119. While the fMRI test–retest reliability has
been mainly investigated from the point of view of
group level studies, here we present analyses and
results for single-subject test–retest
reliability. One important aspect of group level
reliability is that not only does it depend on
between-session variance (test–retest), but also on
between-subject variance. This has partly led to a
debate regarding which reliability metric to use and
how different sources of noise contribute to
between-session variance. Focusing on single subject
reliability allows considering between-session
only. In this study, we measured test–retest
reliability in four behavioural tasks (motor
mapping, covert verb generation, overt word
repetition, and a landmark identification task) to
ensure generalisation of the results and at three
levels of data processing (time-series correlation,
t value variance, and overlap of thresholded maps)
to understand how each step influences the other and
how confounding factors influence reliability at
each of these steps. The contributions of
confounding factors (scanner noise, subject motion,
and coregistration) were investigated using multiple
regression and relative importance analyses at each
step. Finally, to achieve a fuller picture of what
constitutes a reliable task, we introduced a
bootstrap technique of within- vs. between-subject
variance. Our results show that (i) scanner noise
and coregistration errors have little contribution
to between-session variance (ii) subject motion
(especially correlat- ed with the stimuli) can have
detrimental effects on reliability (iii) different
tasks lead to different reliability re- sults. This
suggests that between-session variance in fMRI is
mostly caused by the variability of underlying
cognitive processes and motion correlated with the
stimuli rather than technical limitations of data
processing.}
}
@Article{gorgolewski.EA:13,
author = {Krzysztof J. Gorgolewski and Amos J. Storkey and
Mark E. Bastin and Ian Whittle and Cyril Pernet},
title = {Single subject {fMRI} test–retest reliability
metrics and confounding factors},
journal = NI,
year = 2013,
volume = 69,
pages = {231--243},
abstract = {While the fMRI test–retest reliability has been
mainly investigated from the point of view of group
level studies, here we present analyses and results
for single-subject test–retest reliability. One
important aspect of group level reliability is that
not only does it depend on between-session variance
(test–retest), but also on between-subject
variance. This has partly led to a debate regarding
which reliability metric to use and how different
sources of noise contribute to between-session
variance. Focusing on single subject reliability
allows considering between-session only. In this
study, we measured test–retest reliability in four
behavioural tasks (motor mapping, covert verb
generation, overt word repetition, and a landmark
identification task) to ensure generalisation of the
results and at three levels of data processing
(time-series correlation, t value variance, and
overlap of thresholded maps) to understand how each
step influences the other and how confounding
factors influence reliability at each of these
steps. The contributions of confounding factors
(scanner noise, subject motion, and coregistration)
were investigated using multiple regression and
relative importance analyses at each step. Finally,
to achieve a fuller picture of what constitutes a
reliable task, we introduced a bootstrap technique
of within- vs. between-subject variance. Our results
show that (i) scanner noise and coregistration
errors have little contribution to between-session
variance (ii) subject motion (especially correlat-
ed with the stimuli) can have detrimental effects on
reliability (iii) different tasks lead to different
reliability re- sults. This suggests that
between-session variance in fMRI is mostly caused by
the variability of underlying cognitive processes
and motion correlated with the stimuli rather than
technical limitations of data processing.}
}
@Book{greenstein.greenstein:00,
author = {Ben Greenstein and Adam Greenstein},
title = {Color Atlas of Neuroscience: Neuroanatomy and
Neurophysiology},
publisher = {Thieme},
year = 2000,
address = {Stuttgart}
}
@Article{grgic.EA:16,
author = {Regina Gregori Grgi{\vc} and Enrico Calore and
Claudio {de'Sperati}},
title = {Covert enaction at work: Recording the continuous
movements of visuospatial attention to visible or
imagined targets by means of Steady-State Visual
Evoked Potentials {(SSVEPs)}},
journal = {Cortex},
year = 2016,
volume = 74,
pages = {31--52},
annote = {Whereas overt visuospatial attention is customarily
measured with eye tracking, covert attention is
assessed by various methods. Here we exploited
Steady-State Visual Evoked Potentials (SSVEPs) e the
oscillatory responses of the visual cortex to
incoming flickering stimuli e to record the
movements of covert visuospatial attention in a way
operatively similar to eye tracking (attention
tracking), which allowed us to compare motion obser-
vation and motion extrapolation with and without eye
movements. Observers fixated a central dot and
covertly tracked a target oscillating horizontally
and sinusoidally. In the background, the left and
the right halves of the screen flickered at two
different fre- quencies, generating two SSVEPs in
occipital regions whose size varied reciprocally as
observers attended to the moving target. The two
signals were combined into a single quantity that
was modulated at the target frequency in a
quasi-sinusoidal way, often clearly visible in
single trials. The modulation continued almost
unchanged when the target was switched off and
observers mentally extrapolated its motion in
imagery, and also when observers pointed their
finger at the moving target during covert tracking,
or imagined doing so. The amplitude of modulation
during covert tracking was ~25--30\% of that
measured when observers followed the target with
their eyes. We used 4 electrodes in
parieto-occipital areas, but similar results were
achieved with a single electrode in Oz. In a second
experiment we tested ramp and step motion. During
overt tracking, SSVEPs were remarkably accurate,
showing both saccadic-like and smooth pursuit-like
modulations of cortical responsiveness, although
during covert tracking the modulation
deteriorated. Covert tracking was better with
sinusoidal motion than ramp motion, and better with
moving targets than stationary ones. The clear
modulation of cortical responsiveness recorded
during both overt and covert tracking, identical for
motion observation and motion extrapolation,
suggests to include covert attention movements in
enactive theories of mental imagery.}
}
@Article{haak.EA:14,
author = {Koen V. Haak and Dave R.M. Langers and Remco Renken
and Pim {van Dijk} and Johannes Borgstein and Frans
W. Cornelissen},
title = {Abnormal visual field maps in human cortex: A
mini-review and a case report},
journal = {Cortex},
year = 2014,
volume = 56,
pages = {14--25},
abstract = {Human visual cortex contains maps of the visual
field. Much research has been dedicated to answering
whether and when these visual field maps change if
critical components of the visual circuitry are
damaged. Here, we first provide a focused
mini-review of the functional magnetic resonance
imaging (fMRI) studies that have evaluated the human
cortical visual field maps in the face of retinal
lesions, brain injury, and atypical retinocortical
projections. We find that there is a fair body of
research that has found abnormal fMRI activity, but
also that this abnormal activity does not
necessarily stem from cortical remapping. The
abnormal fMRI activity can often be explained in
terms of task effects and/or the uncovering of
normally hidden system dynamics. We then present the
case of a 16-year-old patient who lost the entire
left cerebral hemisphere at age three for treatment
of chronic focal en- cephalitis (Rasmussen syndrome)
and intractable epilepsy. Using an fMRI retinotopic
mapping procedure and population receptive field
(pRF) modeling, we found that (1) despite the long
period since the hemispherectomy, the retinotopic
organization of early visual cortex remained
unaffected by the removal of an entire cerebral
hemisphere, and (2) the intact lateral occipital
cortex contained an exceptionally large
representation of the center of the visual
field. The same method also indicates that the
neuronal receptive fields in these lateral occipital
brain regions are extraordinarily small. These
features are clearly abnormal, but again they do not
necessarily stem from cortical remapping. For
example, the abnormal features can also be explained
by the notion that the hemispherectomy took place
during a critical period in the development of the
lateral occipital cortex and therefore arrested its
normal development. Thus, caution should be
exercised when interpreting abnormal fMRI activity
as a marker of cortical remapping; there are often
other explanations.}
}
@Book{haberland:07,
author = {Catherine Haberland},
title = {Clinical Neuropathology: text and color atlas},
publisher = {Demos Medical Publishing},
year = 2007,
address = {New York, USA}
}
@Article{hadjikhani.EA:01,
author = {Nouchine Hadjikhani and Margarita {Sanchez del Rio}
and Ona Wu and Denis Schwartz and Dick Bakker and
Bruce Fischl and Kenneth K. Kwong and F. Michael
Cutrer and Bruce R. Rosen and Roger B. H. Tootell
and A. Gregory Sorensen and Michael A. Moskowitz},
title = {Mechanisms of migraine aura revealed by functional
{MRI} in human visual cortex},
journal = PNAS,
year = 2001,
volume = 98,
number = 8,
pages = {4687--4692},
abstract = {Cortical spreading depression (CSD) has been
suggested to under- lie migraine visual
aura. However, it has been challenging to test this
hypothesis in human cerebral cortex. Using
high-field func- tional MRI with near-continuous
recording during visual aura in three subjects, we
observed blood oxygenation level-dependent (BOLD)
signal changes that demonstrated at least eight
character- istics of CSD, time-locked to percept
onset of the aura. Initially, a focal increase in
BOLD signal (possibly reflecting vasodilation),
developed within extrastriate cortex (area
V3A). This BOLD change progressed contiguously and
slowly (3.5 1.1 mm min) over occipital cortex,
congruent with the retinotopy of the visual per-
cept. Following the same retinotopic progression,
the BOLD signal then diminished (possibly reflecting
vasoconstriction after the initial vasodilation), as
did the BOLD response to visual activation. During
periods with no visual stimulation, but while the
subject was experiencing scintillations, BOLD signal
followed the retino- topic progression of the visual
percept. These data strongly sug- gest that an
electrophysiological event such as CSD generates the
aura in human visual cortex.}
}
@Article{henriksson.EA:07,
author = {L. Henriksson and A. Raninen and R. N{\"a}s{\"a}nen
and L. Hyv{\"a}rinen and S. Vanni},
title = {Training-induced cortical representation of a
hemianopic hemifield},
journal = JNNP,
year = 2007,
volume = 78,
pages = {74--81},
abstract = {Background: Patients with homonymous hemianopia
often have some residual sensitivity for visual
stimuli in their blind hemifield. Previous imaging
studies suggest an important role for extrastriate
cortical areas in such residual vision, but results
of training to improve vision in patients with
hemianopia are conflicting. Objective: To show that
intensive training with flicker stimulation in the
chronic stage of stroke can reorganise visual
cortices of an adult patient. Methods: A
61-year-old patient with homonymous hemianopia was
trained with flicker stimulation, starting 22 months
after stroke. Changes in functioning during training
were documented with magnetoencephalography, and the
cortical organisation after training was examined
with functional magnetic resonance imaging (fMRI).
Results: Both imaging methods showed that, after
training, visual information from both hemifields
was processed mainly in the intact hemisphere. The
fMRI mapping results showed the representations of
both the blind and the normal hemifield in the same
set of cortical areas in the intact hemisphere, more
specifically in the visual motion-sensitive area V5,
in a region around the superior temporal sulcus and
in retinotopic visual areas V1 (primary visual
cortex), V2, V3 and V3a. Conclusions: Intensive
training of a blind hemifield can induce cortical
reorganisation in an adult patient, and this case
shows an ipsilateral representation of the trained
visual hemifield in several cortical areas,
including the primary visual cortex. }
}
@Article{hirsch.EA:00,
author = {Joy Hirsch and Maximilian I. Ruge and Karl H.S. Kim
and Denise D. Correa and Jonathan D. Victor and
Norman R. Relkin and Douglas R. Labar and George
Krol and Mark H. Bilsky and Mark M. Souweidane and
Lisa M. DeAngelis},
title = {An Integrated Functional Magnetic Resonance Imaging
Procedure for Preoperative Mapping of Cortical Areas
Associated with Tactile, Motor, Language, and Visual
Functions},
journal = {Neurosurgery},
year = 2000,
volume = 47,
pages = {711--722},
abstract = {OBJECTIVE: To evaluate an integrated battery of
preoperative functional magnetic resonance imaging
(fMRI) tasks developed to identify cortical areas
associated with tactile, motor, language, and visual
functions. METHODS: Sensitivity of each task was
determined by the probability that a targeted region
was activated for both healthy volunteers (n 63) and
surgical patients with lesions in these critical
areas (n 125). Accuracy of each task was determined
by the correspondence between the fMRI maps and
intraoperative electrophysiological measurements,
including somatosensory evoked potentials (n 16),
direct cortical stimulation (n 9), and language
mapping (n 5), and by preoperative Wada tests (n 13)
and visual field examinations (n 6). RESULTS: For
healthy volunteers, the overall sensitivity was
100\% for identification of the central sulcus,
visual cortex, and putative Wernicke’s area, and
93\% for the putative Broca’s area (dominant
hemisphere). For patients with tumors affecting
these regions of interest, task sensitivity was 97\%
for identification of the central sulcus, 100\% for
the visual cortex, 91\% for the putative Wernicke’s
area, and 77\% for the putative Broca’s area. These
sensitivities were enhanced by the use of multiple
tasks to target related functions. Concordance of
the fMRI maps and intraoperative
electrophysiological measurements was observed
whenever both techniques yielded maps and Wada and
visual field examinations were consistent with fMRI
results. CONCLUSION: This integrated fMRI task
battery offers standardized and noninvasive
preoperative maps of multiple critical functions to
facilitate assessment of surgical risk, planning of
surgical routes, and direction of conventional,
intraoperative electrophysiological
procedures. Thus, a greater range of structural and
functional relationships is brought to bear in the
service of optimal outcomes for neurosurgery.}
}
@Article{huisman.EA:06,
author = {Thierry A. G. M. Huisman and Thomas Loenneker and
Gerd Barta and Matthias E. Bellemann and Juergen
Hennig and Joachim E. Fischer and Kamil A. Il'yasov},
title = {Quantitative diffusion tensor MR imaging of the
brain: field strength related variance of apparent
diffusion coefficient {(ADC)} and fractional
anisotropy {(FA)} scalars},
journal = ER,
year = 2006,
volume = 16,
number = 8,
pages = {1651--1658},
abstract = {The objectives were to study the "impact" of the
magnetic field strength on diffusion tensor imaging
(DTI) metrics and also to determine whether
magnetic-field-related differences in T2-relaxation
times of brain tissue influence DTI
measurements. DTI was performed on 12 healthy
volunteers at 1.5 and 3.0 Tesla (within 2 h) using
identical DTI scan parameters. Apparent diffusion
coefficient (ADC) and fractional anisotropy (FA)
values were measured at multiple gray and white
matter locations. ADC and FA values were compared
and analyzed for statistically significant
differences. In addition, DTI measurements were
performed at different echo times (TE) for both
field strengths. ADC values for gray and white
matter were statistically significantly lower at 3.0
Tesla compared with 1.5 Tesla (% change between
-1.94% and -9.79%). FA values were statistically
significantly higher at 3.0 Tesla compared with 1.5
Tesla (% change between +4.04 and 11.15%). ADC and
FA values are not significantly different for TE=91
ms and TE=125 ms. Thus, ADC and FA values vary with
the used field strength. Comparative clinical
studies using ADC or FA values should consequently
compare ADC or FA results with normative ADC or FA
values that have been determined for the field
strength used.}
}
@Article{iacoboni.zaidel:04,
author = {Marco Iacoboni and Eran Zaidel},
title = {Interhemispheric visuo-motor integration in humans:
the role of the superior parietal cortex},
journal = {Neuropsychologia},
year = 2004,
volume = 42,
number = 4,
pages = {419--425},
abstract = {We used event-related functional magnetic resonance
imaging (fMRI) to investigate the neural correlates
of basic interhemispheric visuo-motor
integration. In a simple reaction time task,
subjects responded to lateralized left and right
light flashes with unimanual left and right hand
responses. Typically, reaction times are faster for
uncrossed responses (that is, visual stimulus and
response hand on the same side) than for crossed
responses (that is, visual stimulus and response
hand on opposite sides). The chronometric difference
between crossed and uncrossed responses is called
crossed–uncrossed difference (CUD) and it is
typically taken to represent a behavioral estimate
of interhemispheric transfer time. The fMRI results
obtained in normal right-handers show that the
crossed conditions yielded greater activity,
compared to the uncrossed conditions, in bilateral
prefrontal, bilateral dorsal premotor, and right
superior parietal areas. These results suggest that
multiple transfers between the hemispheres occur in
parallel at the functional levels of sensory–motor
integration (posterior parietal), decision-making
(prefrontal) and preparation of motor response
(premotor). To test the behavioral significance of
these multiple transfers, we correlated the
individual CUDs with the difference in signal
intensity between crossed and uncrossed responses in
the prefrontal, dorsal premotor, and right superior
parietal activated areas. The analyses demonstrated
a strong correlation between the CUD and signal
intensity difference between crossed and uncrossed
responses in the right superior parietal
cortex. These data suggest a critical role of the
superior parietal cortex in interhemispheric
visuo-motor integration.}
}
@InCollection{iacoboni:05,
author = {Marco Iacoboni},
title = {Divided Attention in the Normal and the Split Brain:
Chronometry and Imaging},
booktitle = {Neurobiology of Attention},
publisher = {Academic Press},
year = 2005,
editor = {Laurent Itti and Geraint Rees and John K. Tsotsos},
pages = {363--367},
address = {San Diego, California, US},
abstract = {Divided attention is the ability to integrate in
parallel multiple stimuli. A relevant experimental
effect that has been studied for almost a century is
the redundant target effect. When multiple copies of
the same stimulus are presented to subjects, in
choice, go no-go, and even a simple reaction time
task, reaction times (RT) tend to be faster,
compared to RT to a single copy of the
stimulus. Paradoxically, this effect is larger in
split-brain patients when two stimuli are presented
in the two opposite hemifields. Recent RT and
imaging studies reviewed in this chapter suggest
that cortico-subcortical interactions between the
superior colliculus and the extrastriate cortex,
that are modulated by the corpus callosum, are
reflected in different levels of activation in
dorsal premotor cortex during divided attention
tasks and can account for the paradoxical
facilitation observed in split-brain patients.}
}
@Article{itti.EA:98,
author = {Laurent Itti and Christof Koch and Ernst Niebur},
title = {A Model of Saliency-Based Visual Attention for Rapid
Scene Analysis},
journal = {IEEE Transactions on Pattern Analysis and Machine
Intelligence,},
year = 1998,
volume = 20,
number = 11,
pages = {1254--1259},
abstract = {A visual attention system, inspired by the behavior
and the neuronal architecture of the early primate
visual system, is presented. Multiscale image
features are combined into a single topographical
saliency map. A dynamical neural network then
selects attended locations in order of decreasing
saliency. The system breaks down the complex problem
of scene understanding by rapidly selecting, in a
computationally efficient manner, conspicuous
locations to be analyzed in detail.}
}
@Book{jacobson.marcus:11,
author = {Stanley Jacobson and Elliott M. Marcus},
title = {Neuroanatomy
for the Neuroscientist},
publisher = {Springer},
year = 2011,
address = {New York, USA},
edition = {Second}}
@Article{james.EA:03,
author = {Thomas W. James and Jody Culham and G. Keith
Humphrey and A. David Milner and Melvyn A. Goodale},
title = {Ventral occipital lesions impair object recognition
but not object‐directed grasping: an {fMRI} study},
journal = {Brain},
year = 2003,
volume = 126,
pages = {2463--2475},
abstract = {D.F., a patient with severe visual form agnosia, has
been the subject of extensive research during the
past decade. The fact that she could process visual
input accurately for the purposes of guiding action
despite being unable to perform visual
discriminations on the same visual input inspired a
novel interpretation of the functions of the two
main cortical visual pathways or ‘streams’. Within
this theoretical context, the authors proposed that
D.F. had suffered severe bilateral damage to her
occipitotemporal visual system (the ‘ventral
stream’), while retaining the use of her
occipitoparietal visual system (the ‘dorsal
stream’). The present paper reports a direct test of
this idea, which was initially derived from purely
behavioural data, before the advent of modern
functional neuroimaging. We used functional MRI to
examine activation in her ventral and dorsal streams
during object recognition and object‐directed
grasping tasks. We found that D.F. showed no
difference in activation when presented with line
drawings of common objects compared with scrambled
line drawings in the lateral occipital cortex (LO)
of the ventral stream, an area that responded
differentially to these stimuli in healthy
individuals. Moreover, high‐resolution anatomical
MRI showed that her lesion corresponded bilaterally
with the location of LO in healthy participants. The
lack of activation with line drawings in
D.F. mirrors her poor performance in identifying the
objects depicted in the drawings. With coloured and
greyscale pictures, stimuli that she can identify
more often, D.F. did show some ventral‐stream
activation. These activations were, however, more
widely distributed than those seen in control
participants and did not include LO. In contrast to
the absent or abnormal activation observed during
these perceptual tasks, D.F. showed robust
activation in the expected dorsal stream regions
during object grasping, despite considerable atrophy
in some regions of the parietal lobes. In
particular, an area in the anterior intraparietal
sulcus was activated more for grasping an object
than for just reaching to that object, for both
D.F. and controls. In conclusion, we have been able
to confirm directly that D.F.’s visual form agnosia
is associated with extensive damage to the ventral
stream, and that her spared visuomotor skills are
associated with visual processing in the dorsal
stream.}
}
@Article{jamison.EA:15,
author = {Keith W. Jamison and Abhrajeet V. Roy and Sheng He
and Stephen A. Engel and Bin He},
title = {{SSVEP} signatures of binocular rivalry during
simultaneous {EEG and fMRI}},
journal = JNMeth,
year = 2015,
volume = 243,
pages = {53--62},
abstract = {Binocular rivalry is a perceptual phenomenon that
arises when two incompatible images are presented
separately, one to each eye, and the observer
experiences involuntary perceptual alternations
between the two images. If the two images are
flickering at two distinct frequencies,
electroencephalography (EEG) can be used to track
the frequency-tagged steady-state visually evoked
potential (SSVEP) driven by each image as they
compete for awareness, providing an objective
measure of the subjective perceptual state. This
spontaneous alternation in perceptual dominance is
believed to be driven by neural processes across
widespread regions in the brain, but the real-time
mechanisms of these processes remain unclear.}
}
@Article{janz.EA:00,
author = {Clemens Janz and Christina Schmitt and Oliver Speck
and J{\"u}rgen Hennig},
title = {Comparison of the hemodynamic response to different
visual stimuli in single-event and block stimulation
{fMRI} experiments},
journal = JMRI,
year = 2000,
volume = 12,
pages = {708--714},
abstract = {Experiments with three different types of basic
visual stimulation were performed to compare
cortical activation in single-event and block
trials. Independent of the stimulation paradigm, the
single-event presentation leads to highly consistent
signal responses regarding both the activated
cortical areas and the dynamics of the signal time
course. In contrast, signal time courses during
block paradigms depend on the stimulus applied and
are a complex and nonlinear function of the
single-event responses. Additionally, the initial
dip during the first 2 seconds after stimulus onset
is consistently observed. However, the small
amplitude change (−0.1% to −0.3%) requires signal
averaging to establish statistical significance of
the effect. Furthermore, different patterns of
activation were observed within the primary visual
cortex. In an anterior part of the primary visual
cortex, activation was only observed at the onset
and at the cessation of stimulation involving
luminance changes.}
}
@Article{jenkins.EA:03,
author = {Rob Jenkins and Nilli Lavie and Jon Driver},
title = {Ignoring famous faces: Category-specific dilution of
distractor interference},
journal = PP,
year = 2003,
volume = 65,
number = 2,
pages = {298--309},
abstract = {The extent to which famous distractor faces can be
ignored was assessed in six experiments. Subjects
categorized famous printed target names as those of
pop stars or politicians, while attempting to ignore
a flanking famous face distractor that could be
congruent (e.g., a politician's name and face) or
incongruent (e.g., a politician's name with a pop
star's face). Congruency effects on reaction times
indicated distractor intrusion. An additional,
response-neutral flanker (neither pop star nor
politician) could also be present. Congruency
effects from the critical distractor face were
reduced (diluted) by the presence of an intact
anonymous face, but not by phase-shifted versions,
inverted faces, or meaningful nonface objects. By
contrast, congruency effects from other types of
distracting objects (musical instruments, fruits),
when printed names for these classes were
categorized, were diluted equivalently by intact
faces, phase-shifted faces, or meaningful nonface
objects. Our results suggest that distractor faces
act differently from other types of distractors,
suffering from only face-specific capacity limits.
}
}
@Article{jones.cercignani:10,
author = {Derek K. Jones and Mara Cercignani},
title = {Twenty-five pitfalls in the analysis of diffusion
{MRI} data},
journal = NMR,
year = 2010,
volume = 23,
number = 7,
pages = {803--820},
abstract = {Obtaining reliable data and drawing meaningful and
robust inferences from diffusion MRI can be
challenging and is subject to many pitfalls. The
process of quantifying diffusion indices and
eventually comparing them between groups of subjects
and/or correlating them with other parameters starts
at the acquisition of the raw data, followed by a
long pipeline of image processing steps. Each one of
these steps is susceptible to sources of bias, which
may not only limit the accuracy and precision, but
can lead to substantial errors. This article
provides a detailed review of the steps along the
analysis pipeline and their associated
pitfalls. These are grouped into 1 pre-processing of
data; 2 estimation of the tensor; 3 derivation of
voxelwise quantitative parameters; 4 strategies for
extracting quantitative parameters; and finally 5
intra-subject and inter-subject comparison,
including region of interest, histogram,
tract-specific and voxel-based analyses. The article
covers important aspects of diffusion MRI analysis,
such as motion correction, susceptibility and eddy
current distortion correction, model fitting, region
of interest placement, histogram and voxel-based
analysis. We have assembled 25 pitfalls (several
previously unreported) into a single article, which
should serve as a useful reference for those
embarking on new diffusion MRI-based studies, and as
a check for those who may already be running studies
but may have overlooked some important
confounds. While some of these problems are well
known to diffusion experts, they might not be to
other researchers wishing to undertake a clinical
study based on diffusion MRI.}
}
@Article{kavcic.EA:15,
author = {Voyko Kavcic and Regina L. Triplett and Anasuya Das
and Tim Martin and Krystel R. Huxlin},
title = {Role of inter-hemispheric transfer in generating
visual evoked potentials in {V1}-damaged brain
hemispheres},
journal = {Neuropsychologia},
year = 2015,
volume = 68,
pages = {82--93},
abstract = {Partial cortical blindness is a visual deficit
caused by unilateral damage to the primary visual
cortex, a condition previously considered beyond
hopes of rehabilitation. However, recent data
demonstrate that patients may recover both simple
and global motion discrimination following intensive
training in their blind field. The present
experiments characterized motion-induced neural
activity of cortically blind (CB) subjects prior to
the onset of visual rehabilitation. This was done to
provide information about visual processing
capabilities available to mediate training-induced
visual improvements. Visual Evoked Po- tentials
(VEPs) were recorded from two experimental groups
consisting of 9 CB subjects and 9 age- matched,
visually-intact controls. VEPs were collected
following lateralized stimulus presentation to each
of the 4 visual field quadrants. VEP waveforms were
examined for both stimulus-onset (SO) and motion-
onset (MO) related components in postero-lateral
electrodes. While stimulus presentation to intact
re- gions of the visual field elicited normal SO-P1,
SO-N1, SO-P2 and MO-N2 amplitudes and latencies in
contralateral brain regions of CB subjects, these
components were not observed contralateral to
stimulus presentation in blind quadrants of the
visual field. In damaged brain hemispheres, SO-VEPs
were only recorded following stimulus presentation
to intact visual field quadrants, via
inter-hemispheric transfer. MO-VEPs were only
recorded from damaged left brain hemispheres,
possibly reflecting a native left/right asymmetry in
inter-hemispheric connections. The present findings
suggest that damaged brain hemi- spheres contain
areas capable of responding to visual
stimulation. However, in the absence of training or
rehabilitation, these areas only generate detectable
VEPs in response to stimulation of the intact hemi-
field of vision.}
}
@Article{kentridge.EA:99,
author = {R. W. Kentridge and C. A. Heywood and L. Weiskrantz},
title = {Attention without awareness in blindsight},
journal = PhilTransLonBio,
year = 1999,
volume = 266,
pages = {1805--1811},
abstract = {The act of attending has frequently been equated
with visual awareness. We examined this relationship
in `blindsight'öa condition in which the latter is
absent or diminished as a result of damage to the
primary visual cortex. Spatially selective visual
attention is demonstrated when information that
stimuli are likely to appear at a speci¢c location
enhances the speed or accuracy of detection of
stimuli subsequently presented at that location. In
a blindsight subject, we showed that attention can
confer an advantage in processing stimuli presented
at an attended location, without those stimuli
entering consciousness. Attention could be directed
both by symbolic cues in the subject's spared ¢eld
of vision or cues presented in his blind ¢eld. Cues
in his blind ¢eld were even e¡ective in directing
his attention to a second location remote from that
at which the cue was presented. These indirect cues
were e¡ective whether or not they themselves
elicited non-visual awareness. We concluded that the
spatial selection of information by an attentional
mechanism and its entry into conscious experience
cannot be one and the same process.}
}
@Article{klein.EA:00,
author = {Isabelle Klein and Anne-Lise Paradis and
Jean-Baptiste Poline and Stephen M. Kosslyn},
title = {Transient Activity in the Human Calcarine Cortex
During Visual-Mental Imagery: An Event-Related fMRI
Study},
journal = JoCN,
year = 2000,
volume = 12,
number = {Suppl.2},
pages = {15--23},
abstract = {Although it is largely accepted that visual-mental
imagery and perception draw on many of the same
neural structures, the existence and nature of
neural processing in the primary visual cortex (or
area V1) during visual imagery remains
controversial. We tested two general hypotheses:
The first was that V1 is activated only when images
with many details are formed and used, and the
second was that V1 is activated whenever images are
formed, even if they are not necessarily used to
perform a task. We used event-related functional
magnetic resonance imaging (ER-fMRI) to detect and
char- acterize the activity in the calcarine sulcus
(which contains the primary visual cortex) during
single instances of mental imagery. The results
revealed reproducible transient activity in this
area whenever participants generated or evaluated a
mental image. This transient activity was strongly
enhanced when participants evaluated characteristics
of objects, whether or not details actually needed
to be extracted from the image to perform the task.
These results show that visual imagery processing
commonly involves the earliest stages of the visual
system}
}
@Article{kleiser.EA:01,
author = {R. Kleiser and J. Wittsack and M. Niedeggen and
R. Goebel and P. Stoerig},
title = {Is {V1} Necessary for Conscious Vision in Areas of
Relative Cortical Blindness?},
journal = NI,
year = 2001,
volume = 13,
number = 4,
pages = {654--661},
abstract = {Visual field defects result from postgeniculate
lesions. It is generally assumed that absolute
defects are caused by total destruction or
denervation of primary visual cortex (V1) and that
the degraded but conscious vision that remains or
returns in relative or partial defects is mediated
by compromised V1 cortex that retains a sufficiently
large population of functional neurons. We here
report the results of three patients with
long-standing postgeniculate lesions who underwent
functional magnetic resonance imaging while their
partial defect was stimulated with high-contrast
reversing checkerboard stimuli. Although the
stimulation evoked conscious visual impressions in
all three, in only one patient did it activate
perilesional V1. In the other two we found no
evidence for perilesional activation, indicating
that some conscious vision may return in the absence
of functional ipsilesional V1.}
}
@Article{lamme:03,
author = {Victor A.F. Lamme},
title = {Why visual attention and awareness are different},
journal = TICS,
year = 2003,
volume = 7,
number = 1,
pages = {12--18},
abstract = {Now that the study of consciousness is warmly
embraced by cognitive scientists, much confusion
seems to arise between the concepts of visual
attention and visual awareness. Often, visual
awareness is equated to what is in the focus of
attention. There are, however, two sets of arguments
to separate attention from awareness: a
psychological/theoretical one and a neurobiological
one. By combining these arguments I present
definitions of visual attention and awareness that
clearly distinguish between the two, yet explain why
attention and aware- ness are so intricately
related. In fact, there seems more overlap between
mechanisms of memory and awareness than between
those of attention and awareness.}
}
@Article{lamme:06,
author = {Victor A.F. Lamme},
title = {Towards a true neural stance on consciousness},
journal = TICS,
year = 2006,
volume = 10,
number = 11,
pages = {494--501},
abstract = {Consciousness is traditionally defined in mental or
psychological terms. In trying to find its neural
basis, introspective or behavioral observations are
considered the gold standard, to which neural
measures should be fitted. I argue that this poses
serious problems for under- standing the mind–brain
relationship. To solve these problems, neural and
behavioral measures should be put on an equal
footing. I illustrate this by an example from visual
neuroscience, in which both neural and behavioral
arguments converge towards a coherent scientific
definition of visual consciousness. However, to
accept this definition, we need to let go of our
intuitive or psychological notions of conscious
experience and let the neuroscience arguments have
their way. Only by moving our notion of mind towards
that of brain can progress be made.}
}
@Article{lamme.roelfsema:00,
author = {Victor A.F. Lamme and Pieter R. Roelfsema},
title = {The distinct modes of vision offered by feedforward
and recurrent processing},
journal = TIN,
year = 2000,
volume = 23,
pages = {571--579},
abstract = {An analysis of response latencies shows that when an
image is presented to the visual system, neuronal
activity is rapidly routed to a large number of
visual areas. However, the activity of cortical
neurons is not determined by this feedforward sweep
alone. Horizontal connections within areas, and
higher areas providing feedback, result in dynamic
changes in tuning.The differences between
feedforward and recurrent processing could prove
pivotal in understanding the distinctions between
attentive and pre-attentive vision as well as
between conscious and unconscious vision. The
feedforward sweep rapidly groups feature
constellations that are hardwired in the visual
brain, yet is probably incapable of yielding visual
awareness; in many cases, recurrent processing is
necessary before the features of an object are
attentively grouped and the stimulus can enter
consciousness}
}
@Article{laws.EA:05,
author = {Keith R. Laws and Tim M. Gale and Verity C. Leeson
and John R. Crawford},
title = {When is category specific in {Alzheimer's} disease?},
journal = {Cortex},
year = 2005,
volume = 41,
pages = {452--463},
abstract = {Mixed findings have emerged concerning whether
category-specific disorders occur in Alzheimer’s
disease. Factors that may contribute to these
inconsistencies include: ceiling effects / skewed
distributions for control data in some studies;
differences in the severity of cognitive deficit in
patients; and differences in the type of analysis
(in particular, if and how controls are used to
analyse single case data).We examined picture naming
in Alzheimer’s patients and matched elderly healthy
normal controls in three experiments. These
experiments used stimuli that did and did not
produce ceiling effects / skewed data in
controls. In Experiment 1, we examined for category
effects in individual DAT patients using commonly
used analyses for single cases (χ2 and
z-scores). The different techniques produced quite
different outcomes. In Experiment 2a, we used the
same techniques on a different group of patients
with similar outcomes. Finally, in Experiment 2b, we
examined the same patients but (a) used stimuli that
did not produce ceiling effects / skewed
distributions in healthy controls, and (b) used
statistical methods that did not treat the control
sample as a population. We found that ceiling
effects in controls may markedly inflate the
incidence of dissociations in which living things
are differentially impaired and seriously
underestimate dissociations in the opposite
direction. In addition, methods that treat the
control sample as a population led to inflation in
the overall number of dissociations detected. These
findings have implications for the reliability of
category effects previously reported both in
Alzheimer patients and in other pathologies. In
particular, they suggest that the greater proportion
of living than nonliving deficits reported in the
literature may be an artifact of the methods used.}
}
@Article{li.EA:15,
author = {Fali Li and Yin Tian and Yangsong Zhang and Kan Qiu
and Chunyang Tian and Wei Jing and Tiejun Liu and
Yang Xia and Daqing Guo and Dezhong Yao and Peng Xu},
title = {The enhanced information ow from visual cortex to
frontal area facilitates {SSVEP} response: evidence
from model-driven and data-driven causality
analysis},
journal = SR,
year = 2015,
volume = 5,
pages = 14765,
note = {doi:10.1038/srep14765},
abstract = {The neural mechanism of steady-state visual evoked
potentials (SSVEP) is still not clearly
understood. Especially, only certain frequency
stimuli can evoke SSVEP. Our previous network study
reveals that 8 Hz stimulus that can evoke strong
SSVEP response shows the enhanced linkage strength
between frontal and visual cortex. To further probe
the directed information ow between the two cortex
areas for various frequency stimuli, this paper
develops a causality analysis based on the inversion
of double columns model using particle swarm
optimization (PSO) to characterize the directed
information ow between visual and frontal cortices
with the intracranial rat electroencephalograph
(EEG). The estimated model parameters demonstrate
that the 8 Hz stimulus shows the enhanced
directional information ow from visual cortex to
frontal lobe facilitates SSVEP response, which may
account for the strong SSVEP response for 8 Hz
stimulus. Furthermore, the similar nding is
replicated by data-driven causality analysis. The
inversion of neural mass model proposed in this
study may be helpful to provide the new causality
analysis to link the physiological model and the
observed datasets in neuroscience and clinical
researches.}
}
@Article{liu.EA:10,
author = {Zhongming Liu and Cristina Rios and Nanyin Zhang and
Lin Yang and Wei Chen and Bin He},
title = {Linear and nonlinear relationships between visual
stimuli, {EEG and BOLD fMRI} signals},
journal = NI,
year = 2010,
volume = 50,
pages = {1054--1066},
abstract = {In the present study, the cascaded interactions
between stimuli and neural and hemodynamic responses
were modeled using linear systems. These models
provided the theoretical hypotheses that were tested
against the electroencephalography (EEG) and blood
oxygen level dependent (BOLD) functional magnetic
resonance imaging (fMRI) data recorded from human
subjects during prolonged periods of repeated visual
stimuli with a variable setting of the
inter-stimulus interval (ISI) and visual
contrast. Our results suggest that (1) neural
response is nonlinear only when ISIb0.2 s, (2) BOLD
response is nonlinear with an exclusively vascular
origin when 0.25bISIb4.2 s, (3) vascular response
nonlinearity reflects a refractory effect, rather
than a ceiling effect, and (4) there is a strong
linear relationship between the BOLD effect size and
the integrated power of event-related synaptic
current activity, after modeling and taking into
account the vascular refractory effect. These
conclusions offer important insights into the
origins of BOLD nonlinearity and the nature of
neurovascular coupling, and suggest an effective
means to quantitatively interpret the BOLD signal in
terms of neural activity. The validated cross-modal
relationship between fMRI and EEG may provide a
theoretical basis for the integration of these two
modalities.}
}
@Article{macpherson.EA:09,
author = {Helen Macpherson and Andrew Pipingas and Richard
Silberstein},
title = {A steady state visually evoked potential
investigation of memory and ageing},
journal = BC,
year = 2009,
volume = 69,
pages = {571--579},
abstract = {Old age is generally accompanied by a decline in
memory performance. Specifically, neuroimaging and
electrophysiological studies have revealed that
there are age-related changes in the neural
correlates of episodic and working memory. This
study investigated age-associated changes in the
steady state visu- ally evoked potential (SSVEP)
amplitude and latency associated with memory
performance. Participants were 15 older (59–67
years) and 14 younger (20–30 years) adults who
performed an object working memory (OWM) task and a
contextual recognition memory (CRM) task, whilst the
SSVEP was recorded from 64 electrode
sites. Retention of a single object in the low
demand OWM task was characterised by smaller frontal
SSVEP amplitude and latency differences in older
adults than in younger adults, indic- ative of an
age-associated reduction in neural
processes. Recognition of visual images in the more
difficult CRM task was accompanied by larger, more
sustained SSVEP amplitude and latency decreases over
tem- poral parietal regions in older adults. In
contrast, the more transient, frontally mediated
pattern of activ- ity demonstrated by younger adults
suggests that younger and older adults utilize
different neural resources to perform recognition
judgements. The results provide support for
compensatory processes in the aging brain; at lower
task demands, older adults demonstrate reduced
neural activity, whereas at greater task demands
neural activity is increased.}
}
@Article{malinowski.EA:07,
author = {Peter Malinowski and Sandra Fuchs and Matthias
M. M{\"u}ller },
title = {Sustained division of spatial attention to multiple
locations within one hemifield},
journal = NeuroLett,
year = 2007,
volume = 414,
pages = {65--70},
abstract = {Attending to a location in space significantly
improves stimulus perception at that
location. Everyday experience requires the
deployment of attention to multiple objects at
different locations. Recent empirical evidence
suggests that the “beam” of attention can be divided
between non- contiguous areas of the visual
field. Whether this is only possible when stimuli
are presented in different hemifields and harder, if
not impossible, when stimuli are in the same
hemifield is an ongoing debate. Here we use an
electrophysiological measure of sustained
attentional resource allocation (the steady-state
visual evoked potential, SSVEP) to address this
question. In combination with behavioural data we
demonstrate that splitting the attentional “beam” is
in principle possible within one hemifield. However,
results showed that task performance was in general
lower for same-hemifield presentation as opposed to
our previous study with different-hemifield
presentation [M.M. Mu ̈ller, P. Malinowski,
T. Gruber, S.A. Hillyard, Sustained division of the
attentional spotlight, Nature 424 (2003)
309–312]. SSVEP amplitude showed a mixed pattern of
results for stimuli presented in the upper versus
lower quadrant of the left visual hemifield under
conditions of attending to two separated
locations. Results are discussed in the light of the
bilateral distribution advantage hypothesis and
differences in stimulus salience between the upper
and lower visual field.}
}
@Article{manoach.EA:03,
author = {Dara S. Manoach},
title = {Prefrontal cortex dysfunction during working memory
performance in schizophrenia: reconciling discrepant
findings},
journal = SCZres,
year = 2003,
volume = 60,
number = {2--3},
pages = {285--298},
abstract = {Working memory (WM) deficits are a persistent,
disabling and relatively treatment-resistant feature
of schizophrenia that may underlie many cognitive
deficits and symptoms. They are associated with
prefrontal cortex dysfunction. While most
neuroimaging studies of WM demonstrate “task-related
hypofrontality” in schizophrenic relative to healthy
subjects, several recent studies have reported equal
or increased prefrontal activity. These findings
challenge central assumptions regarding cognitive
deficits and prefrontal cortex dysfunction in
schizophrenia. The goal of this review is to
reconcile these seemingly discrepant
findings. Methodological factors addressed include
the use of intersubject averaging, WM task
parameters and the reliability of the
measures. Factors intrinsic to schizophrenia and
their relevance to the selection of experimental
methods and the interpretation of group data are
also discussed. Both hypo- and hyperfrontality are
hypothesized to be valid and informative reflections
of prefrontal cortex dysfunction in
schizophrenia. Due to the heterogeneity and
variability of both performance and regional
recruitment in schizophrenia, whether individual
data is considered, the level and type of WM demands
and the composition of the sample with regard to
performance deficits all influence study outcome and
contribute to discrepancies. Although the prefrontal
cortex is consistently implicated in WM deficits,
the basis of its dysfunction and its exact
contribution remain unclear. Future work might focus
on delineating the exact WM processes, domains and
components that are deficient. In addition,
variability in behavior and activation might best be
regarded as intrinsic to schizophrenia and having a
neural basis that requires explanation. In
combination with other techniques, neuroimaging can
identify the neural circuitry responsible for WM
deficits and elucidate the contribution of each
anatomical component.}
}
@Article{marshall.EA:08,
author = {Randolph S. Marshall and John J. Ferrera and Anna
Barnes and Xian Zhang and Katherine A. O'Brien and
Mohamad Chmayssani and Joy Hirsch and Ronald
M. Lazar},
title = {Brain Activity Associated With Stimulation Therapy
of the Visual Borderzone in Hemianopic Stroke
Patients},
journal = NRNR,
year = 2008,
volume = 22,
number = 2,
pages = {136--144},
abstract = {BACKGROUND AND OBJECTIVE: Visual restoration therapy
is a home-based treatment program intended to expand
visual fields of hemianopic patients through
repetitive stimulation of the borderzone adjacent to
the blind field. We hypothesized that the training
itself would induce visual field location-specific
changes in the brain's response to stimuli, a
phenomenon demonstrated in animal experiments but
never in humans with brain injury. METHODS: Six
chronic right hemianopic patients underwent
functional magnetic resonance imaging
(fMRI)--responding to stimuli in the trained visual
borderzone versus the nontrained seeing field before
and after 1 month of visual restoration
therapy. Spatially normalized fMRI time-series data
were analyzed in a fixed-effects group analysis
comparing blood oxygen level dependent (BOLD)
activity in the borderzone versus seeing location at
baseline and at 1 month. Percent BOLD change was
measured to determine each condition's contribution
to the time-by-condition interaction. RESULTS:
There was a significant time by condition
interaction manifested as increased BOLD activity
for borderzone detection relative to seeing
detection after the first month of therapy, which
correlated with a relative improvement in response
times in the borderzone location out-of-scanner. The
right inferior and lateral temporal, right
dorsolateral frontal, bilateral anterior cingulate,
and bilateral basal ganglia showed the greatest
response. CONCLUSION: Visual restoration therapy
appears to induce an alteration in brain activity
associated with a shift of attention from the
nontrained seeing field to the trained
borderzone. The effect appears to be mediated by the
anterior cingulate and dorsolateral frontal cortex
in conjunction with other higher order visual areas
in the occipitotemporal and middle temporal
regions. Demonstration of a visual field-specific
training effect on brain activity provides an
important starting point for understanding the
potential for visual therapy in hemianopia.}
}
@Article{marcel:98,
author = {Anthony J. Marcel},
title = {Blindsight and shape perception: deficit of visual
consciousness or of visual function?},
journal = {Brain},
year = 1998,
volume = 121,
pages = {1565--1588},
abstract = {Two people with homonymous right hemianopias were
tested on a number of measures of non-conscious and
conscious perception of shape in the blind field.
Experiment 1 examined preparatory manual adjustments
in grasping objects. Both subjects performed well
above chance not only in three-dimensional location
but also in preforming the hand to the shape, size
and orientation of objects. In Experiment 2 single
upper-case letters were briefly exposed in the blind
field, and subjects made forced choices among 6
alternatives in the sighted field. Performance
improved over blocks of trials and was above chance,
but not dramatically. In Experiment 3 single
upper-case words were briefly presented in the blind
field, and subjects chose which of two words exposed
after in the intact field was semantically closer.
In Experiment 4 subjects had to give the meaning of
single ambiguous words (e.g. BANK) presented both
visually in the intact field and auditorily. Each
ambiguous word was preceded by a single upper-case
word briefly presented in the blind field, biasing
each meaning on different blocks of trials (e.g.
MONEY and RIVER). In Experiment 3, although results
were in the appropriate direction, they were not
consistently well above chance. By contrast, in
Keywords : blindsight, consciousness, shape
perception Introduction Blindsight is the name given
to tacit residual visual capacities in a scotoma,
such as discrimination and localization of visual
stimuli that neurologial patients deny seeing
(Sanders et al ., 1974). It is often taken by
psychologists and philosophers as a deficit of
consciousness (Natsoulas, 1982; Dennett, 1991). It
has also been traditionally studied as a deficit of
visual function, especially with regard to the two-
visual-systems hypothesis (Schneider, 1967; Po ̈ ppel
et al. , 1973), and data do show several functional
deficits, e.g. in form and colour perception (for
reviews see Weiskrantz, 1986, 1990). This raises
several issues. (i) Is blindsight both a deficit of
visual consciousness and (separately) of visual
function(s), or basically a deficit of just one
kind? (ii) Are © Oxford University Press 1998
Experiment 4 both subjects were consistently
semantically biased to a high degree by words in the
blind field. Experiments 2, 3 and 4 taken together
suggest that indirect techniques (priming) are more
sensitive to showing effects of non-conscious
perception than direct ones (forced- choice). More
importantly the experiments indicate that not only
orientation but curvature, structural descriptions
of component strokes and spatial ordering of letters
are registered non-consciously in the blind
field. Experiment 5 examined after-images in the
blind and sighted fields, showing veridical
conscious perception of shape in the blind field
provided it was accompanied by a shape in the
sighted field which together formed a good Gestalt.
Experiment 6 showed conscious perception of illusory
contours spanning the hemifields induced by Kanizsa
figures. The experiments suggest that aspects of
shape are much better perceived in blindsight than
previously thought, that this is independent of
their use in motor control, that the main deficit in
blindsight is one of consciousness, and that the
loss of conscious vision in the blind field is far
from total. The effects and their relationship to
those in other neuropsychological deficits suggest
an intimate link between perceptual consciousness,
attention and object perception.}
}
@Article{marzi.EA:91,
author = {C.A. Marzi and P. Bisiacchi and R. Nicoletti},
title = {Is interhemispheric transfer of visuomotor
information asymmetric? Evidence from a
meta-analysis},
journal = {Neuropsychologia},
year = 1991,
volume = 29,
number = 12,
pages = {1163--1177},
abstract = {Using a meta-analytic procedure we have analysed 16
studies employing a simple unimanual reaction time
(RT) paradigm and lateralized visual stimuli to
provide an estimate of interhemispheric transfer
time in normal right-handed subjects. We found a
significant overall RT advantage of the left visual
field over the right and of the right hand over the
left. These asymmetries can be explained by a
superiority of the right hemisphere for the
detection of simple visual stimuli and by a
corresponding superiority of the left hemisphere for
the execution of the manual response,
respectively. Alternatively, they may be interpreted
as related to an asymmetry of interhemispheric
transmission of visuomotor information, with
transfer from the right hemisphere (side of stimulus
entry) to the left (side of response generation)
faster than in the reverse direction. Although a
direct test of these hypotheses is still lacking, we
think that the evidence available is more in keeping
with the latter possibility.}
}
@Article{marzi.EA:06,
author = {C.A. Marzi and F. Mancini and T. Metitieri and
S. Savazzi},
title = {Retinal eccentricity effects on reaction time to
imagined stimuli},
journal = {Neuropsychologia},
year = 2006,
volume = 44,
number = 8,
pages = {1489--1495},
abstract = {To cast light on the possible neural substrate of
visual imagery we tested normal participants and one
hemianopic patient on simple reaction time (RT) to
real and imagined visual stimuli. In one experiment
participants were to detect as quickly as possible a
luminous square presented at one out of two
different retinal eccentricities. A well known
effect with visual stimuli is that RT is slower for
peripheral versus central stimuli. We found that
imagined stimuli showed an eccentricity effect
similar to that obtained with real stimuli. However,
this was not the case in a patient with a hemianopic
visual field loss (quadrantanopia) as a result of
damage to the optic radiation. Even though the
patient showed no difficulty in imaging stimuli in
the affected hemifield she did not show an
eccentricity effect as was the case in her intact
side. In a second experiment, normal participants
showed faster RT to stimuli of larger size with
either real or imagined stimuli. Overall, these
results show that visual perception and imagination
share a similar visuotopic organisation that is
disrupted following deafferentation of the visual
cortex.}
}
@Article{maus.EA:10,
author = {B{\"a}rbel Maus and Gerard J.P. {Van Breukelen} and
Rainer Goebel and Martijn P.F. Berger},
title = {Optimization of blocked designs in {fMRI} studies},
journal = {Psychometrika},
year = 2010,
volume = 75,
number = 2,
pages = {373--390},
abstract = {Blocked designs in functional magnetic resonance
imaging (fMRI) are useful to localize functional
brain areas. A blocked design consists of different
blocks of trials of the same stimulus type and is
charac- terized by three factors: the length of
blocks, i.e., number of trials per blocks, the
ordering of task and rest blocks, and the time
between trials within one block. Optimal design
theory was applied to find the opti- mal combination
of these three design factors. Furthermore,
different error structures were used within a
general linear model for the analysis of fMRI data,
and the maximin criterion was applied to find
designs which are robust against misspecification of
model parameters.}
}
@Article{mazzi.EA:14,
author = {Chiara Mazzi and Francesca Mancini and Silvia
Savazzi},
title = {Can {IPS} reach visual awareness without {V1}?
Evidence from {TMS} in healthy subjects and
hemianopic patients},
journal = {Neuropsychologia},
year = 2014,
volume = 64,
pages = {134--144},
abstract = {TMS of the occipital cortex can elicit conscious
visual percepts, the so-called phosphenes, i.e. the
experience of flashes of light in the absence of an
external stimulus. Previous evidence has shown that
phosphenes can be elicited by TMS of the
intraparietal sulcus (IPS). Here, we tested whether
IPS-phosphenes are generated without any
contribution from the occipital cortex. In
Experiment 1, healthy subjects showed that parietal
phosphenes were reliable different in terms of
threshold, highly variable in size and, in contrast
to the occipital ones, they did not change in
lateralization within the visual field. Moreover, to
strengthen these results and to ascertain whether
feedback to primary visual cortex is necessary for
visual awareness to emerge, in Experiment 2, we
induced phosphenes by applying TMS over the parietal
cortex of the lesioned hemisphere in two hemianopic
patients with a complete destruction of primary
visual cortex. For both patients we found that they
could perceive phosphenes, that a psychophysical
threshold function could be created and that this
function was not different from that obtained with
healthy subjects. In addition, they could reliably
draw the phosphenes and position them within their
blind field and they could reliably score the
phenomenical characteristics of their phosphenes
both in terms of vividness and brightness in a
manner similar to healthy subjects. The two
brain-damaged patients have thus shown that
stimulation of visual areas within the intraparietal
sulcus of their lesioned hemisphere, can, in fact,
elicit conscious visual percepts. These results seem
to demonstrate that TMS-induced visual phenomenology
over IPS can generate conscious visual percepts and,
more importantly, that it does so independently of
any contributions from the primary visual cortex.}
}
@Article{mcgonigle.EA:00,
author = {D. J. {McGonigle} and A. M. Howseman and
B. S. Athwal and K. J. Friston and
R. S. J. Frackowiak and A. P. Holmes},
title = { Variability in {fMRI}: An Examination of
Intersession Differences},
journal = NI,
year = 2000,
volume = 11,
pages = {708--734},
abstract = {The results from a single functional magnetic reso-
nance imaging session are typically reported as
indic- ative of the subject’s functional
neuroanatomy. Under- lying this interpretation is
the implicit assumption that there are no responses
specific to that particular session, i.e., that the
potential variability of response between sessions
is negligible. The present study sought to examine
this assumption empirically. A total of 99 sessions,
comprising 33 repeats of simple motor, visual, and
cognitive paradigms, were collected over a period of
2 months on a single male subject. For each
paradigm, the inclusion of session-by-condition
inter- actions explained a significant amount of
error vari- ance (P < 0.05 corrected for multiple
comparisons) over a model assuming a common
activation magni- tude across all sessions. However,
many of those vox- els displaying significant
session-by-condition interac- tions were not seen in
a multisession fixed-effects analysis of the same
data set; i.e., they were not acti- vated on average
across all sessions. Most voxels that were both
significantly variable and activated on av- erage
across all sessions did not survive a random-
effects analysis (modeling between-session
variance). We interpret our results as demonstrating
that correct inference about subject responses to
activation tasks can be derived through the use of a
statistical model which accounts for both within-
and between-session variance, combined with an
appropriately large ses- sion sample size. If
researchers have access to only a single session
from a single subject, erroneous conclu- sions are a
possibility, in that responses specific to this
single session may be claimed to be typical
responses for this subject.}
}
@Article{mcgonigle:12,
author = {David J. {McGonigle}},
title = {Test–retest reliability in {fMRI}: Or how I learned
to stop worrying and love the variability},
journal = NI,
year = 2012,
volume = 62,
pages = {1116--1120},
abstract = {This paper briefly recounts the details of one of
the first studies of whole brain, single subject
variability in functional Magnetic Resonance Imaging
(fMRI). In this paper I will not attempt to provide
an over- view of fMRI reliability, but will instead
revisit the choices we made in performing our
experiment as we did.}
}
@Article{megumi.EA:15,
author = {Fukuda Megumi and Bahador Bahrami and Ryota Kanai
and Geraint Rees},
title = {Brain activity dynamics in human parietal regions
during spontaneous switches in bistable perception},
journal = NI,
year = 2015,
volume = 107,
pages = {190--197},
abstract = {The neural mechanisms underlying conscious visual
perception have been extensively investigated using
bistable perception paradigms. Previous functional
magnetic resonance imaging (fMRI) and transcranial
magnetic stimula- tion (TMS) studies suggest that
the right anterior superior parietal (r-aSPL) and
the right posterior superior parietal lobule
(r-pSPL) have opposite roles in triggering
perceptual reversals. It has been proposed that
these two areas are part of a hierarchical network
whose dynamics determine perceptual
switches. However, how these two parietal regions
interact with each other and with the rest of the
brain during bistable perception is not known. Here,
we investigated such a model by recording brain
activity using fMRI while participants viewed a
bistable structure- from-motion stimulus. Using
dynamic causal modeling (DCM), we found that
resolving such perceptual ambiguity was specifically
associated with reciprocal interactions between
these parietal regions and V5/MT. Strikingly, the
strength of bottom-up coupling between V5/MT to
r-pSPL and from r-pSPL to r-aSPL predicted
individual mean dominance duration. Our findings are
consistent with a hierarchical predictive coding
model of parietal involve- ment in bistable
perception and suggest that visual information
processing underlying spontaneous perceptual
switches can be described as changes in connectivity
strength between parietal and visual cortical
regions.}
}
@Article{mele.EA:08,
author = {Sonia Mele and Silvia Savazzi and Carlo A. Marzi and
Giovanni Berlucchi},
title = {Reaction time inhibition from subliminal cues: Is it
related to inhibition of return?},
journal = {Neuropsychologia},
year = 2008,
volume = 46,
pages = {810--819},
abstract = {Task-irrelevant visual cues with near zero
visibility proved apt to retard reaction time for
the detection of supraliminal visual targets
presented at the cued location. The time course of
the effect was similar to that of the so-called
inhibition-of return (IOR), which is assumed to be
due to the withdrawal of attention from the
inhibited location. However the present subliminal
cues consistently failed to induce an RT
facilitation prior to the RT inhibition, contrary to
what would be expected if the cue were able to
attract attention to the cued location. Since the RT
inhibition from subliminal cues could not be
attributed to the withdrawal of attention from the
cued location, it can be argued that such cues acted
both outside of consciousness and without the
influence of attention. Therefore, the RT inhibitory
effect seems best accounted for by an automatic,
unconscious and attention-independent
self-inhibition of response tendencies instructed by
irrelevant information, akin to that postulated by
(Eimer, M., & Schlaghecken, F. (1998). Effects of
masked stimuli on motor activation: behavioural and
electrophysiological evidence.}
}
@Article{miki.EA:05,
author = {Atsushi Miki and Grant T. Liu and Edward
J. Modestino and Gabrielle R. Bonhomme and
Chia-Shang J. Liu and John C. Haselgrove},
title = {Decreased Lateral Geniculate Nucleus Activation in
Retrogeniculate Hemianopia Demonstrated by
Functional Magnetic Resonance Imaging at 4Tesla},
journal = {Ophthalmologica},
year = 2005,
volume = 219,
pages = {11--19},
abstract = {Functional magnetic resonance imaging (fMRI) can de-
tect lateral geniculate nucleus (LGN) activation. We
stud- ied LGN function in 5 patients with
retrogeniculate hom- onymous hemianopia using fMRI
at 4.0 Tesla during binocular visual
stimulation. Decreased activation of vi- sual cortex
and LGN on the side of the lesion was ob- served in
all 5 patients.These findings suggest that ret-
rogeniculate lesions are associated with decreased
activation of the LGN, due to retrograde
degeneration or a functional decrease caused by
decreased feedback from ipsilateral visual cortex.}
}
@Book{milner.goodale:95,
author = {A. David Milner and Melvyn A. Goodale},
title = {The visual brain in action},
publisher = {Oxford Science Publications},
year = 1995,
series = {Oxford Psychology Series no.27},
address = {Oxford}}
@Article{morland.EA:02,
author = {A. B. Morland and M. B. Hoffmann and M. Neveu and
G. E. Holder},
title = {Abnormal visual projection in a human albino studied
with functional magnetic resonance imaging and
visual evoked potentials},
journal = JNNP,
year = 2002,
volume = 72,
pages = {523--526},
abstract = {The albino visual pathway is abnormal in that many
fibres from the temporal retina project to the
contralateral visual cortex. The visual projections
in a human albino and a control have been
investigated with fMRI and VEP during independent
visual stimulation of both hemifields. Activity in
the occipital cortex in the normal was contralateral
to the stimulated visual field, whereas it was
contralateral to the stimulated eye in the albino,
independent of the stimulated visual field. Thus,
the albino visual cortex is activated not only by
stimulation in the contralateral visual field, but
also by abnormal input representing the ipsilateral
visual field. These novel findings help elucidate
the nature of albino misrouting. }
}
@Article{morland.EA:04,
author = {Antony B. Morland and Sandra L{\^e} and Erin Carroll
and Michael B. Hoffmann and Alidz Pambakian},
title = {The role of spared calcarine cortex and lateral
occipital cortex in the responses of human
hemianopes to visual motion},
journal = JoCN,
year = 2004,
volume = 16,
number = 2,
pages = {204--218},
abstract = {Some patients, who are rendered perimetrically blind
in one hemifield by cortical lesions, nevertheless
exhibit residual visual capacities within their
field defects. The neural mechanism that mediates
the residual visual responses has remained the topic
of considerable debate. One explanation posits the
subcortical visual pathways that bypass the primary
visual cortex and innervate the extrastriate visual
areas as the substrate that underlies the residual
vision. The other explanation is that small islands
of the primary visual cortex remain intact and
provide the signals for residual vision. We have
performed behavioral and functional magnetic
resonance imaging experiments to investigate the
validity of the two explanations of residual
vision. Our behavioral experiments indicated that of
the seven hemianopes tested, two had the ability to
discriminate the direction of a drifting
grating. This residual visual response was shown
with fMRI to be the result of spared islands of
calcarine cortical activity in one of the
hemianopes, whereas only lateral occipital activity
was documented in the other patient. These results
indicate that the underlying neural correlates of
residual vision can vary between patients. Moreover,
our study emphasizes the necessity of ruling out the
presence of islands of preserved function and
primary visual cortex before assigning residual
visual capacities to the properties of visual
pathways that bypass the primary visual cortex.}
}
@Article{mueller.EA:16,
author = {Matthias M. M{\"u}ller and Mireille Trautmann and
Christian Keitel},
title = {Early Visual Cortex Dynamics during Top–Down
Modulated Shifts of Feature-Selective Attention},
journal = JoCN,
year = 2016,
volume = 28,
number = 4,
pages = {643--655},
annote = {Shifting attention from one color to another color
or from color to another feature dimension such as
shape or orientation is imperative when searching
for a certain object in a cluttered scene. Most
attention models that emphasize feature-based
selection implicitly assume that all shifts in
feature-selective attention underlie identical
temporal dynamics. Here, we re- corded time courses
of behavioral data and steady-state visual evoked
potentials (SSVEPs), an objective
electrophysiological measure of neural dynamics in
early visual cortex to investigate temporal dynamics
when participants shifted attention from color or
orientation toward color or orientation,
respectively. SSVEPs were elicited by four random
dot kinematograms that flickered at different
frequencies. Each random dot kinematogram was
composed of dashes that uniquely combined two fea-
tures from the dimensions color (red or blue) and
orientation (slash or backslash). Participants were
cued to attend to one feature (such as color or
orientation) and respond to coherent motion targets
of the to-be-attended feature. We found that shifts
toward color occurred earlier after the shifting cue
com- pared with shifts toward orientation,
regardless of the original feature (i.e., color or
orientation). This was paralleled in SSVEP amplitude
modulations as well as in the time course of behav-
ioral data. Overall, our results suggest different
neural dynamics during shifts of attention from
color and orientation and the respective shifting
destinations, namely, either toward color or toward
orientation.}
}
@Article{nelles.EA:02,
author = {Gereon Nelles and Guido Widman and Armin {de Greiff}
and Anette Meistrowitz and Albena Dimitrova and
Johannes Weber and Michael Forsting and Joachim
Esser and H. Christoph Diener},
title = {Brain Representation of Hemifield Stimulation in
Poststroke Visual Field Defects},
journal = {Stroke},
year = 2002,
volume = 33,
pages = {1286--1293},
abstract = {Background and Purpose— Plasticity in extended,
parallel, or reciprocal operating networks is well
recognized. Changes in neuronal activity after
lesions to distinct localized structures, such as
the primary visual cortex, are less well
characterized. We investigated the cortical
reorganization in patients with poststroke visual
field defects using blood oxygen level–dependent
functional MRI. Methods— Brain activation was
measured in 7 patients with a single occipital
cortical lesion and partially recovered hemianopia
and in 7 age-matched control subjects. Differences
in activation between rest and visual hemifield
stimulation were assessed with statistical
parametric mapping (SPM’99). Results— In normal
subjects, significant activation was found in the
contralateral primary visual cortex and bilaterally
in the extrastriate cortex. During hemifield
stimulation of the unaffected side of stroke
patients, a similar pattern was found compared with
that seen in control subjects. During stimulation of
the hemianopic side, bilateral activation was seen
within the extrastriate cortex, stronger in the
ipsilateral hemisphere. The primary visual cortex
was not significantly activated in either hemisphere
during stimulation of the hemianopic side.
Conclusions— Visual field defects after stroke are
associated with bilateral activation of the
extrastriate visual cortex. This pattern of
activation indicates altered neuronal activity in
the visual system. Further investigation is
necessary to determine the relationship between
functional reorganization and recovery of lost
visual function after poststroke hemianopia. }
}
@Article{nelles.EA:07,
author = {Gereon Nelles and Armin {de Greiff} and Anja
Pscherer and Michael Forsting and Horst Gerhard and
Joachim Esser and H. Christoph Diener},
title = {Cortical activation in hemianopia after stroke},
journal = NeuroLett,
year = 2007,
volume = 426,
number = 1,
pages = {34--38},
abstract = {Changes in neuronal activity of the visual cortex
have been described in patients with hemianopia. The
anatomical areas that are involved in neuroplastic
changes have not been studied in a larger group of
stroke patients with a homogenous structural
pathology of the visual cortex. Brain activation was
measured in 13 patients with a single ischemic
lesion of the striate cortex and partially recovered
hemianopia and in 13 age-matched control subjects
using blood oxygen level dependent (BOLD) functional
magnetic resonance imaging (fMRI). Differences in
activation between rest and visual hemifield
stimulation were assessed with statistical
parametric mapping using group and multi-group
studies. In normal subjects, the most significant
activation was found in the contralateral primary
visual cortex (area 17) and bilaterally in the
extrastriate cortex (areas 18 and 19). In patients,
these areas were also activated when the intact
hemifield was stimulated. During stimulation of the
hemianopic side, bilateral activation was seen
within the extrastriate cortex, stronger in the
ipsilateral (contralesional) hemisphere. Stimulation
of the hemianopic visual field is associated with
ipsilateral activation of the extrastriate visual
cortex. This pattern of activation suggests
extensive neuronal plasticity within the visual
cortex after postgeniculate ischemic lesions and may
have implications for therapeutic interventions.}
}
@Article{norcia.EA:15,
author = {Anthony M. Norcia and L. Gregory Appelbaum and
Justin M. Ales and Benoit R. Cottereau and Bruno
Rossion},
title = {The steady-state visual evoked potential in vision
research: A review},
journal = JoVis,
year = 2015,
volume = 15,
number = 6,
pages = {1--46},
abstract = {Periodic visual stimulation and analysis of the
resulting steady-state visual evoked potentials were
first introduced over 80 years ago as a means to
study visual sensation and perception. From the
first single-channel recording of responses to
modulated light to the present use of sophisticated
digital displays composed of complex visual stimuli
and high-density recording arrays, steady-state
methods have been applied in a broad range of
scientific and applied settings. The purpose of this
article is to describe the fundamental stimulation
paradigms for steady-state visual evoked potentials
and to illustrate these principles through research
findings across a range of applications in vision
science.}
}
@Article{,
author = {Robert Oostenveld and Pascal Fries and Eric Maris
and Jan-Mathijs Schoffelen},
title = {{FieldTrip}: Open Source Software for Advanced
Analysis of {MEG, EEG}, and Invasive
Electrophysiological Data},
journal = CIN,
year = {2011},
OPTkey = {},
OPTvolume = {},
OPTnumber = {},
OPTpages = {},
OPTmonth = {},
OPTnote = {doi:10.1155/2011/156869},
abstract = {This paper describes FieldTrip, an open source
software package that we developed for the analysis
of MEG, EEG, and other electrophysiological
data. The software is implemented as a MATLAB
toolbox and includes a complete set of consistent
and user- friendly high-level functions that allow
experimental neuroscientists to analyze experimental
data. It includes algorithms for simple and advanced
analysis, such as time-frequency analysis using
multitapers, source reconstruction using dipoles,
distributed sources and beamformers, connectivity
analysis, and nonparametric statistical permutation
tests at the channel and source level. The
implementation as toolbox allows the user to perform
elaborate and structured analyses of large data sets
using the MATLAB command line and batch
scripting. Furthermore, users and developers can
easily extend the functionality and implement new
algorithms. The modular design facilitates the reuse
in other software packages.}
}
@Article{palomares.EA:12,
author = {Melanie Palomares and Justin M. Ales and Alex
R. Wade and Benoit R. Cottereau and Anthony
M. Norcia},
title = {Distinct effects of attention on the neural
responses to form and motion processing: A {SSVEP}
source-imaging study},
journal = JoVis,
year = 2012,
volume = 12,
number = 10,
pages = {1--14},
abstract = {We measured neural responses to local and global
aspects of form and motion stimuli using
frequency-tagged, steady-state visual evoked
potentials (SSVEPs) combined with magnetic resonance
imaging (MRI) data. Random dot stimuli were used to
portray either dynamic Glass patterns (Glass, 1969)
or coherent motion displays. SSVEPs were used to
estimate neural activity in a set of fMRI-defined
visual areas in each subject. To compare activity
associated with local versus global processing, we
analyzed two frequency components of the SSVEP in
each visual area: the high temporal frequency at
which the local dots were updated (30 Hz) and the
much lower frequency corresponding to updates in the
global structure (0.83 Hz). Local and global
responses were evaluated in the context of two
different behavioral tasks—subjects had to either
direct their attention toward or away from the
global coherence of the stimuli. The data show that
the effect of attention on global and local
responses is both stimulus and visual area
dependent. When attention was directed away from
stimulus coherence, both local and global responses
were higher in the coherent motion than Glass
pattern condition. Directing attention to coherence
in Glass patterns enhanced global activity in areas
LOC, hMTþ, V4, V3a, and V1, while attention to
global motion modulated responses by a smaller
amount in a smaller set of areas: V4, hMTþ, and
LOC. In contrast, directing attention towards
stimulus coherence weakly increased local responses
to both coherent motion and Glass patterns. These
results suggest that visual attention differentially
modulates the activity of early visual areas at both
local and global levels of structural encoding.}
}
@Article{paramei.sabel:08,
author = {Galina V. Paramei and Bernhard A. Sabel},
title = {Contour-integration deficits on the intact side of
the visual field in hemianopia patients},
journal = BBR,
year = 2008,
volume = 188,
pages = {109--124},
abstract = {Objective: Visual impairments in hemianopia are
thought to be exclusively caused by the reduced
visual field size. However, the primary lesion may
affect the contralateral hemisphere through damage
of interhemispheric projections. The question
therefore arises if the presumed “intact” hemifield
is perceptually impaired. Methods: Three hemianopia
patients and three matched controls carried out a
Yes/No figure detection task with their intact side
of the visual field. The figure (square) contours
were composed of non-contiguous Gabor patches
embedded in a random patch array of different
background densities (low, Δ = 2; high, Δ =
1). Response accuracy and reaction times were
recorded. Results: A temporal–parietal patient
revealed figure detection impairments, with accuracy
rate,77\% (Δ=2) and 53\% (Δ=1),belowcompared control
values. An occipital patient was comparable to his
match: 99\% (Δ = 2); 84\% (Δ = 1). Both patients
exhibited frequent false alarms to random patterns
and required longer presentation times to perform
the task. In the third patient, with optic tract
lesion, figure detection was nearly normal at low
density (92\%, Δ = 2) but impaired at noisy
background (62\%, Δ = 1). Conclusion: The “intact”
visual field in hemianopes is impaired in detection
of incomplete figures embedded in a noisy
background. This deficit may be caused by damage to
higher visual centers and/or loss of
interhemispheric interactions.}
}
@Article{pastor.EA:03,
author = {Maria A. Pastor and Julio Artieda and Javier Arbizu
and Miguel Valencia and Jose C. Masdeu},
title = {Human Cerebral Activation during Steady-State
Visual-Evoked Responses},
journal = JoN,
year = 2003,
volume = 23,
number = 3,
pages = {11621--11627},
abstract = {Flicker stimuli of variable frequency (2-90 Hz)
elicit a steady-state visual-evoked response (SSVER)
in the electroencephalogram (EEG) with the same
frequency as the stimulus. In humans, the amplitude
of this response peaks at ∼15 Hz, decreasing at
higher stimulation frequencies. It was not known
whether this peak response corresponds to increased
synaptic activity in the visual cortex or to other
mechanisms [for instance, the temporal coherence
(phase summation) of evoked responses]. We studied
the SSVER in 16 normal volunteers by means of visual
stimulation at 14 different frequencies (from 5 to
60 Hz) while recording the EEG. In nine subjects of
the group, we measured regional cerebral blood flow
(rCBF) with positron emission tomography (PET)-H215O
at rest and during visual stimulation at five
different frequencies: 5, 10, 15, 25, and 40 Hz. We
confirmed that the amplitude of the SSVER in
occipital regions peaks at 15 Hz
stimulation. Applying to the PET rCBF data a
contrast weighted by the amplitude of the SSVER, we
determined that the primary visual cortex rCBF
follows an activation pattern similar to the
SSVER. This finding suggests that the amplitude of
the SSVER corresponds to increased synaptic
activity, specifically in Brodmann's area
17. Additionally, this study showed that visual
stimulation at 40 Hz causes selective activation of
the macular region of the visual cortex, and that a
region in the dorsal aspect of the Crus I lobule of
the left cerebellar hemisphere is activated during
repetitive visual stimulation. }
}
@Article{perez.EA:13,
author = {C{\'e}line Perez and Carole Peyrin and C{\'e}line
Cav{\'e}zianand Olivier Coubard and Florent Caetta
and Noa Raz and Netta Levin and Ga{\"e}lle Doucet
and Fr{\'e}d{\'e}ric Andersson and Micha{\"e}l
Obadia and Olivier Gout and Fran{\,c}oise H{\'e}ran
and Julien Savatovsky and Sylvie Chokron},
title = {An {fMRI} Investigation of the Cortical Network
Underlying Detection and Categorization Abilities in
Hemianopic Patients},
journal = BT,
year = 2013,
volume = 26,
number = 2,
pages = {264--277},
note = {DON'T HAVE},
abstract = {The current study aims to investigate visual scene
perception and its neuro-anatomical correlates for
stimuli presented in the central visual field of
patients with homonymous hemianopia, and thereby to
assess the effect of a right or a left occipital
lesion on brain reorganization. Fourteen healthy
participants, three left brain damaged (LBD)
patients with right homonymous hemianopia and five
right brain damaged (RBD) patients with left
homonymous hemianopia performed a visual detection
task (i.e. “Is there an image on the screen?”) and a
categorization task (i.e. “Is it an image of a
highway or a city?”) during a block-designed
functional magnetic resonance imaging recording
session. Cerebral activity analyses of the posterior
areas—the occipital lobe in particular—highlighted
bi-hemispheric activation during the detection task
but more lateralized, left occipital lobe activation
during the categorization task in healthy
participants. Conversely, in patients, the same
network of activity was observed in both
tasks. However, LBD patients showed a predominant
activation in their right hemisphere (occipital lobe
and posterior temporal areas) whereas RBD patients
showed a more bilateral activation (in the occipital
lobes). Overall, our preliminary findings suggest a
specific pattern of cerebral activation depending on
the task instruction in healthy participants and
cerebral reorganization of the posterior areas
following brain injury in hemianopic patients which
could depend upon the side of the occipital lesion.}
}
@Article{perez.chokron:14,
author = {C{\'e}line Perez and Sylvie Chokron},
title = {Rehabilitation of homonymous hemianopia: insight
into blindsight},
journal = FIN,
year = 2014,
volume = 8,
number = 82,
note = {doi:10.3389/fnint.2014.00082},
annote = {Strong evidence of considerable plasticity in
primary sensory areas in the adult cortex, and of
dramatic cross-modal reorganization in visual areas,
after short- or long-term visual deprivation has
recently been reported. In the context of patient
rehabilitation, this scientifically challenging
topic takes on urgent clinical relevance, especially
given the lack of information about the role of such
reorganization on spared or newly emerged visual
performance. Amongst the most common visual field
defects found upon unilateral occipital damage of
the primary visual cortex is homonymous hemianopia
(HH), a perfectly symmetric loss of vision in both
eyes. Traditionally, geniculostriate lesions were
considered to result in complete and permanent
visual loss in the topographically related area of
the visual field (Huber, 1992). However, numerous
studies in monkeys, and later, in humans, have
demonstrated that despite destruction of the striate
cortex, or even following a hemispherectomy, some
patients retain a certain degree of unconscious
visual function, known as blindsight. Accordingly,
there have recently been attempts to restore visual
function in patients by stimulating unconscious
preserved blindsight capacities. Herein we review
different visual rehabilitation techniques designed
for brain-damaged patients with visual field
loss. We discuss the hypothesis that explicit
(conscious) visual detection can be restored in the
blind visual field by harnessing implicit
(unconscious) visual capacities. The results that we
summarize here underline the need for early
diagnosis of cortical visual impairment (CVI), and
the urgency in rehabilitating such deficits, in
these patients. Based on the research precedent, we
explore the link between implicit (unconscious)
vision and conscious perception and discuss possible
mechanisms of adaptation and plasticity in the
visual cortex.}
}
@Article{perlstein.EA:03,
author = {William M. Perlstein and Michael A. Cole and Michael
Larson and Kiesa Kelly and Paul Seignourel and
Andreas Keil},
title = {Steady-state visual evoked potentials reveal
frontally-mediated working memory activity in
humans},
journal = NeuroLett,
year = 2003,
volume = 342,
pages = {191--195},
abstract = {Steady-state visual evoked potentials (SSVEPs)
reflect power changes at the stimulus driving
frequency and have been used to assess brain
activity reflecting cognitive processing. Only one
study has demonstrated SSVEP modulation associated
with working memory (WM), and none have compared the
spatial localization of SSVEP modulations during WM
performance with other brain imaging methods. Here
we examined WM-related activity recorded with
dense-array SSVEPs, analyzed using low resolution
electromagnetic tomography, and compared the results
to our previous findings using functional magnetic
resonance imaging (fMRI). WM was associated with
increased SSVEP activity over the right dorsolateral
prefrontal cortex, paralleling our previous fMRI
findings. Frontal WM-related SSVEP power correlated
selectively with task performance. These results
demonstrate the utility of SSVEPs for studying
representational aspects of cognition.}
}
@Article{pessoa.EA:03,
author = {Luiz Pessoa and Sabine Kastner and Leslie
G. Ungerleider},
title = {Neuroimaging Studies of Attention: From Modulation
of Sensory Processing to Top-Down Control},
journal = JoN,
year = 2003,
volume = 23,
number = 10,
pages = {3990--3998},
abstract = {What we perceive depends critically on where we
direct our attention. For example, attention to a
location dramatically improves the accuracy and
speed of detecting a target at that
location. Attention has been shown not only to
increase perceptual sensitivity for target
discrimination but also to reduce the interference
caused by nearby distracters. Moreover, attention is
highly flexible and can be deployed in a manner that
best serves the organism's momentary behavioral
goals: to locations, to visual features, or to
objects. Attention can also be based on internal
goals (e.g., finding a familiar face in the crowd)
or depend on the external environment (e.g., as when
a loud alarm sounds). A large body of evidence
exists from both neurophysiology and functional
magnetic resonance imaging (fMRI) concerning the
neural mechanisms subserving attention. In this
review, we focus on the parallels and differences
that exist between findings revealed by these two
techniques. We also highlight important
contributions to the field of attention that have
been brought about by fMRI studies. We discuss the
effects of attention on activity within areas of
visual cortex, as well as the evidence for the
existence of source areas exerting top-down
attentional control that are thought to provide
biasing signals that are observed in target areas in
visual cortex. In general, in linking single-cell
physiology and fMRI studies, it is assumed that the
effects observed with fMRI directly reflect the
summed responses of large populations of
neurons. However, recent studies, including the
seminal work by Logothetis and colleagues
(Logothetis et al., 2001; Logothetis, 2003), have
shown that the mapping between these two domains is
not so simple. It has been suggested that blood
oxygenation level-dependent (BOLD) signals reflect
the incoming inputs into an area as well as the
processing of this input information by the local
cortical circuitry, including excitatory and
inhibitory interneurons. Thus, in some cases fMRI
may reveal significant activation that may have no
counterpart in single-cell physiology. In such
cases, local field potentials (LFPs), which also
reflect both input signals and local intracortical
processing, appear to correlate better with fMRI
signals. Interestingly, the acquisition of LFPs by
physiologists is becoming more prevalent (Fries et
al., 2001) and may help bridge the gap between
results from single-cell and fMRI studies. }
}
@Article{peterson.EA:14,
author = {Dwight J. Peterson and Gennadiy Gurariy and
Gabriella G. Dimotsantos and Hector Arciniega and
Marian E. Berryhill and Gideon P. Caplovitz},
title = {The steady-state visual evoked potential reveals
neural correlates of the items encoded into visual
working memory},
journal = {Neuropsychologia},
year = 2014,
volume = 63,
pages = {145--153},
abstract = {Visual working memory (VWM) capacity limitations are
estimated to be ~4 items. Yet, it remains unclear
why certain items from a given memory array may be
successfully retrieved from VWM and others are
lost. Existing measures of the neural correlates of
VWM cannot address this question because they
measure the aggregate processing of the entire
stimulus array rather than neural signatures of
individual items. Moreover, this cumulative
processing is usually measured during the delay
period, thereby reflecting the allocation of neural
resources during VWM maintenance. Here, we use the
steady- state visual evoked potential (SSVEP) to
identify the neural correlates of individual stimuli
at VWM encoding and test two distinct hypotheses:
the focused-resource hypothesis and the
diffuse-resource hypothesis, for how the allocation
of neural resources during VWM encoding may
contribute to VWM capacity limitations. First, we
found that SSVEP amplitudes were larger for stimuli
that were later remembered than for items that were
subsequently forgotten. Second, this pattern
generalized so that the SSVEP amplitudes were also
larger for the unprobed stimuli in correct compared
to incorrect trials. These data are consistent with
the diffuse-resource view in which attentional
resources are broadly allocated across the whole
stimulus array. These results illustrate the
important role encoding mechanisms play in limiting
the capacity of VWM.}
}
@Article{plow.EA:12,
author = {Ela B. Plow and Souzana N. Obretenova and Felipe
Fregni and Alvaro Pascual-Leone and Lotfi
B. Merabet},
title = {Comparison of Visual Field Training for Hemianopia
With Active Versus Sham Transcranial Direct Cortical
Stimulation},
journal = NNR,
year = 2012,
volume = 26,
number = 6,
pages = {616--626},
abstract = {Background. Vision Restoration Therapy (VRT) aims to
improve visual field function by systematically
training regions of residual vision associated with
the activity of suboptimal firing neurons within the
occipital cortex. Transcranial direct current
stimulation (tDCS) has been shown to modulate
cortical excitability. Objective. Assess the
possible efficacy of tDCS combined with
VRT. Methods. The authors conducted a randomized,
double-blind, demonstration-of-concept pilot study
where participants were assigned to either VRT and
tDCS or VRT and sham. The anode was placed over the
occipital pole to target both affected and
unaffected lobes. One hour training sessions were
carried out 3 times per week for 3 months in a
laboratory. Outcome measures included objective and
subjective changes in visual field, recording of
visual fixation performance, and vision-related
activities of daily living (ADLs) and quality of
life (QOL). Results. Although 12 participants were
enrolled, only 8 could be analyzed. The VRT and tDCS
group demonstrated significantly greater expansion
in visual field and improvement on ADLs compared
with the VRT and sham group. Contrary to
expectations, subjective perception of visual field
change was greater in the VRT and sham group. QOL
did not change for either group. The observed
changes in visual field were unrelated to
compensatory eye movements, as shown with fixation
monitoring. Conclusions. The combination of
occipital cortical tDCS with visual field
rehabilitation appears to enhance visual functional
outcomes compared with visual rehabilitation
alone. TDCS may enhance inherent mechanisms of
plasticity associated with training. }
}
@Article{price.EA:06,
author = {Cathy J. Price and Jenny Crinion and Karl
J. Friston},
title = {Design and Analysis of {fMRI} Studies With
Neurologically Impaired Patients},
journal = JMRI,
year = 2006,
volume = 23,
pages = {816--826},
abstract = {Functional neuroimaging can be used to characterize
two types of abnormality in patients with
neurological deficits: abnormal functional
segregation and abnormal functional integration. In
this paper we consider the factors that in- fluence
the experimental design, analysis, and interpreta-
tion of such studies. With respect to experimental
design, we emphasize that: 1) task selection is
constrained to tasks the patient is able to perform
correctly, and 2) the most sensitive designs entail
presenting stimuli of the same type close
together. In terms of data preprocessing, prior to
statistical analysis, we note that structural
pathology may call for constraints on nonlinear
transformations, used by spatial normalization, to
prevent distortion of intact tissue. This means that
one may have to increase spatial smooth- ing to
reduce the impact of inaccurate normalization. Im-
portant issues in statistical modeling concern the
first level of analysis (estimation of activation
within subject), which has to distinguish correct
from incorrect responses. At the second level
(between subjects), inference should be based on
between-subjects variance. Provided that these and
other constraints are met, deficits in functional
segregation are indicated when activation in one or
a set of regions is higher or lower in patients
relative to control subjects. In contrast, deficits
in functional integration are implied when the
influence of one brain region on another is stronger
or weaker in patients relative to control subjects.}
}
@Article{ptak.schnider:11,
author = {Radek Ptak and Armin Schnider},
title = {The attention network of the human brain: Relating
structural damage associated with spatial neglect to
functional imaging correlates of spatial attention},
journal = {Neuropsychologia},
year = 2011,
volume = 49,
pages = {3063--3070},
abstract = {Functional imaging studies of spatial attention
regularly report activation of the intraparietal
sulcus (IPS) and dorsal premotor cortex including
the frontal eye fields (FEF) in tasks requiring
overt or covert shifting of attention. In contrast,
lesion-overlap studies of patients with spatial
neglect – a syndrome character- ized by severe
impairments of spatial attention – show that the
critical damage concerns more ventral regions,
comprising the inferior parietal lobule, the
temporal–parietal junction (TPJ), and the superior
temporal gyrus. We performed voxel-based
lesion-symptom mapping of 29 right-hemisphere stroke
patients, using several performance indices derived
from a cueing task as measures of spatial
attention. In contrast to previous studies, we
focused our analyses on eight regions of interest
defined according to results of previous functional
imaging studies. A direct comparison of neglect with
control patients revealed that neglect was
associated with damage to the TPJ, the middle
frontal gyrus, and the posterior IPS. The latter
region was also a significant predictor of the
degree of contralesional slowing of target detection
and the extent to which ipsilesional distracters
captured attention of neglect patients. Finally,
damage to the FEF and posterior IPS was negatively
correlated with the tendency of neglect patients to
ori- ent attention toward behaviourally relevant
distracters. These findings support the results of
functional imaging studies of spatial attention and
provide evidence for a network account of neglect,
according to which attentional selection of relevant
environmental stimuli and the reorienting of
attention result from dynamic interactions between
the IPS, the dorsal premotor cortex, and the TPJ.}
}
@Article{ptito.EA:99,
author = {M. Ptito and P. Johannsen and J. Faubert and
A. Gjedde},
title = {Activation of Human Extrageniculostriate Pathways
after Damage to Area {V1}},
journal = NI,
year = 1999,
volume = 9,
number = 1,
pages = {97--107},
abstract = {We have used positron emission tomography (PET) to
specify the cortical and subcortical structures
activated following visual stimulation of the
scotomatous field in a patient with an asymmetric
bilateral developmental anomaly of the visual
cortex. Computerized perimetry indicated a left
visual field defect only although MRI and18FDG-PET
scans showed abnormalities in both occipital
lobes. The visual stimuli were semicircular gratings
moving in opposite directions on a dynamic
random-dot background. They were specifically
constructed to eliminate intra- and extraocular
light scatter and to optimize the activation of
extra-striate cortical areas and their projecting
subcortical relays. For anatomical localization PET
images were coregistered to the subject's MRI in
Talairach coordinates. After subtraction of the
baseline conditions from the stimulation conditions,
at-statistic map was created on a voxel-by-voxel
basis. Stimulation of the scotomatous hemifield
yielded significant activations of Brodmann cortical
areas 18–19 and 47 as well as the pulvinar thalami
of the left hemisphere, in addition to a less
prominent activation in the right
hemisphere. Stimulation of the intact hemifield
produced significant activation of Brodmann cortical
areas 30 and 47 of the left hemisphere. These
results suggest that in the absence of area V1,
residual vision observed in the blind hemifield
could be mediated by a retinofugal pathway to
extrastriate cortex via the pulvinar.}
}
@Article{raemaekers.EA:11,
author = {M. Raemaekers and D. P. Bergsmaand R. J. A. {van
Wezel} and G. J. {van der Wildt} and A. V. {van den
Berg}},
title = {Effects of Vision Restoration Training on Early
Visual Cortex in Patients With Cerebral Blindness
Investigated With Functional Magnetic Resonance
Imaging},
journal = JNeurophys,
year = 2011,
volume = 105,
pages = {872--882},
abstract = {Cerebral blindness is a loss of vision as a result
of postchiasmatic damage to the visual
pathways. Parts of the lost visual field can be
restored through training. However, the neuronal
mechanisms through which training effects occur are
still unclear. We therefore assessed
training-induced changes in brain function in eight
patients with cerebral blindness. Visual fields were
measured with perimetry and retinotopic maps were
acquired with functional magnetic resonance imaging
(fMRI) before and after vision restoration
training. We assessed differences in hemodynamic re-
sponses between sessions that represented changes in
amplitudes of neural responses and changes in
receptive field locations and sizes. Perimetry
results showed highly varied visual field recovery
with shifts of the central visual field border
ranging between 1 and 7°. fMRI results showed that,
although retinotopic maps were mostly stable over
sessions, there was a small shift of receptive field
locations toward a higher eccentricity after
training in addition to increases in receptive field
sizes. In patients with bilateral brain activation,
these effects were stronger in the affected than in
the intact hemisphere. Changes in receptive field
size and location could account for limited visual
field recovery ( 1°), although it could not account
for the large increases in visual field size that
were observed in some patients. Furthermore, the
retinotopic maps strongly matched perimetry mea-
surements before training. These results are taken
to indicate that local visual field enlargements are
caused by receptive field changes in early visual
cortex, whereas large-scale improvement cannot be
ex- plained by this mechanism.}
}
@Article{raemaekers.EA:12,
author = {M. Raemaekers and S. {du Plessis} and N.F. Ramsey
and J.M.H. Weusten and M. Vink},
title = {Test–retest variability underlying {fMRI}
measurements},
journal = NI,
year = 2012,
volume = 60,
pages = {717--727},
abstract = {Introduction: A high test–retest reliability is of
pivotal importance for many disciplines in fMRI
research. To assess the current limits of fMRI
reliability, we estimated the variability in true
underlying Blood Oxygen Level Dependent (BOLD)
activation, with which we mean the variability that
would be found in the theoret- ical case when we
could obtain an unlimited number of scans in each
measurement. Methods: In this test–retest study,
subjects were scanned twice with one week apart,
while performing a vi- sual and a motor inhibition
task. We addressed the nature of the variability in
the underlying BOLD signal, by separating for each
brain area and each subject the between-session
differences in the spatial pattern of BOLD
activation, and the global (whole brain) changes in
the amplitude of the spatial pattern of BOLD
activation. Results: We found evidence for changes
in the true underlying spatial pattern of BOLD
activation for both tasks across the two
sessions. The sizes of these changes in pattern
activation were approximately 16\% of the total
activation within the pattern, irrespective of brain
area and task. After spatial smoothing, this vari-
ability was greatly reduced, which suggests it takes
place at a small spatial scale. The mean
between-session differences in the amplitude of
activation across the whole brain were 13.8\% for
the visual task and 23.4\% for the motor inhibition
task. Conclusions: Between-session changes in the
true underlying spatial pattern of BOLD activation
are always present, but occur at a scale that is
consistent with partial voluming effects or spatial
distortions. We found no evidence that the
reliability of the spatial pattern of activation
differs systematically between brain
areas. Consequently, between-session changes in the
amplitude of activation are probably due to global
ef- fects. The observed variability in amplitude
across sessions warrants caution when interpreting
fMRI esti- mates of height of brain activation. A
Matlab implementation of the used algorithm is
available for download at
www.ni-utrecht.nl/downloads/ura.}
}
@Article{raninen.EA:07,
author = {A. Raninen and S. Vanni and L. Hyv{\"a}rinen and
R. N{\"a}s{\"a}nen},
title = {Temporal sensitivity in a hemianopic visual field
can be improved by long-term training using flicker
stimulation},
journal = JNNP,
year = 2007,
volume = 78,
pages = {66--73},
note = {doi:10.1136/jnnp.2006.099366 },
abstract = {Background: Blindness of a visual half-field
(hemianopia) is a common symptom after
postchiasmatic cerebral lesions. Although hemianopia
severely limits activities of daily life, current
clinical practice comprises no training of visual
functions in the blind hemifield. Objective: To
find out whether flicker sensitivity in the blind
hemifield can be improved with intensive training,
and whether training with flicker stimulation can
evoke changes in cortical responsiveness. Methods:
Two men with homonymous hemianopia participated in
the experiments. They trained with flicker stimuli
at 30° or with flickering letters at 10°
eccentricity twice a week for a year, and continued
training with more peripheral stimuli
thereafter. Neuromagnetic responses were registered
at 1–2-month intervals, and the Goldmann perimetry
was recorded before, during and after training.
Results: Flicker sensitivity in the blind hemifield
improved to the level of the intact hemifield within
30° eccentricity in one participant and 20°
eccentricity in the other. Flickering letters were
recognised equally at 10° eccentricity in the blind
and intact hemifields. Improvement spread from the
stimulated horizontal meridian to the whole
hemianopic field within 30°. Before training,
neuromagnetic recordings showed no signal above the
noise level in the hemianopic side. During training,
evoked fields emerged in both participants. No
changes were found in the Goldmann perimetry.
Discussion: Results show that sensitivity to flicker
could be fully restored in the stimulated region,
that improvement in sensitivity spreads to the
surrounding neuronal networks, and that, during
training, accompanying changes occurred in the
neuromagnetic fields. }
}
@Article{raposo.EA:11,
author = {Nicolas Raposo and Alexandra S{\'e}verac Cauquil and
Jean Fran{\,c}ois Albucher and Blandine Acket and
Simona Celebrini and J{\'e}r{\'e}mie Pariente and
Christophe Cognard and Isabelle Loubinoux and
Fran{\,c}ois Chollet},
title = {Poststroke conscious visual deficit: clinical course
and changes in cerebral activations},
journal = {Neurorehabil Neural Repair},
year = 2011,
volume = 25,
number = 8,
pages = {703--710},
annote = {BACKGROUND AND PURPOSE: Little is known about the
outcome and recovery mechanisms of visual perception
after a focal lesion of the occipital lobe in
humans, especially after stroke. In this study, the
authors aimed to describe the clinical course and
the neural substrates of conscious perceptive visual
deficit after posterior cerebral artery infarct.
METHODS: The authors prospectively included 8
patients (7 men and 1 woman; mean age, 64.6 ± 18
years) with visual deficit induced by partial damage
of the striate cortex related to acute posterior
cerebral artery infarct. Conscious perception of
color and motion was assessed from the acute phase
to the third month. Functional magnetic resonance
imaging was performed to investigate neural
substrates of visual recovery. RESULTS: In the
acute phase of stroke, visual deficiency was global
(3/8 patients), selective to color (4/8 patients),
or selective to motion (1/8 patients). During the
follow-up, visual performance increased with respect
to color (from 29\% to 70\%; P < .005) and with
respect to motion (from 47\% to 74\%; P <
.005). Despite a lack of ipsilesional V1 area
activation in the acute phase, activations in this
area and in the contralesional extrastriate cortex
were obtained during follow-up. Both ipsilesional
and contralesional V4 activations were correlated
with better outcome. CONCLUSIONS: Extensive visual
recovery occurs early after partial acute posterior
cerebral artery infarct. Spared islands in
ipsilesional V1 area and transcallosal pathways
might be involved in poststroke visual recovery.}
}
@Article{regan.spekreijse:86,
author = {D. Regan and H. Spekreijse},
title = {Evoked potentials in vision research 1961--86},
journal = VisRes,
year = 1986,
volume = 26,
pages = {1461--1480}
}
@Article{regan:09,
author = {D. Regan},
title = {Some early uses of evoked brain responses in
investigations of human visual function},
journal = VisRes,
year = 2009,
volume = 49,
pages = {882--897},
abstract = {In the context of the technical possibilities of the
time, this paper describes early attempts to employ
visual-evoked potentials (VEPs) as a tool for
investigating human visual function, focussing on
the con- tributions of Henk Spekreijse and his
colleagues. The topics covered are as follows:
attempts to distin- guish between true
pattern-specific VEPs and the effects of responses
to changes in local luminance; retinal rivalry and
interocular sustained suppression; the implications
of VEPs elicited by equiluminant chromatic patterns;
VEPs specific to real and apparent motion; stereo
VEPs; identification of a visual– auditory
convergence area in the human brain.}
}
@Article{reitsma.EA:13,
author = {Danielle C. Reitsma and Jedidiah Mathis and John
L. Ulmer and Wade Mueller and Mary J. Maciejewski
and Edgar A. DeYoe},
title = {Atypical retinotopic organization of visual cortex
in patients with central brain damage: congenital
and adult onset},
journal = JoN,
year = 2013,
volume = 33,
number = 32,
pages = {13010--13024},
abstract = {It remains unclear to what extent retinotopic maps
can undergo large-scale plasticity following damage
to human visual cortex. The literature has
predominately focused on retinotopic changes in
patients with retinal pathologies or congenital
brain malformations. Yet, damage to the adult visual
cortex itself is common in cases such as stroke,
tumor, or trauma. To address this issue, we used a
unique database of fMRI vision maps in patients with
adult-onset (n=25) and congenital (n=2) pathology of
the visual cortex. We identified atypical
retinotopic organization in three patients (two with
adult-onset, and one with congenital pathology)
consisting of an expanded ipsilateral field
representation that was on average 3.2 times greater
than healthy controls. The expanded representations
were located at the vertical meridian borders
between visual areas such as V1/V2. Additionally,
two of the three patients had apparently an ectopic
(topographically inconsistent) representation of the
ipsilateral field within lateral occipital cortex
that is normally associated with visual areas V3/V3A
(and possibly other areas). Both adult-onset cases
had direct damage to early visual cortex itself
(rather than to the afferent drive only), resulting
in a mostly nonfunctional hemisphere. The congenital
case had severe cortical malformation of the visual
cortex and was acallosal. Our results are consistent
with a competitive model in which unilateral damage
to visual cortex or disruption of the transcallosal
connections removes interhemispheric suppression
from retino-geniculate afferents in intact visual
cortex that represent the vertical meridian and
ipsilateral visual field.}
}
@Article{ritchie.EA:12,
author = {Kay L. Ritchie and Amelia R. Hunt and Arash
Sahraie},
title = {Trans-saccadic priming in hemianopia: Sighted-field
sensitivity is boosted by a blind-field prime},
journal = {Neuropsychologia},
year = 2012,
volume = 50,
pages = {997--1005},
abstract = {We experience visual stability despite shifts of the
visual array across the retina produced by eye move-
ments. A process known as remapping is thought to
keep track of the spatial locations of objects as
they move on the retina. We explored remapping in
damaged visual cortex by presenting a stimulus in
the blind field of two patients with
hemianopia. When they executed a saccadic eye
movement that would bring the stimulated location
into the sighted field, reported awareness of the
stimulus increased, even though the stimulus was
removed before the saccade began and so never
actually fell in the sighted field. Moreover, when a
location was primed by a blind-field stimulus and
then brought into the sighted field by a saccade,
detection sensitivity for near-threshold targets
appearing at this location increased
dramatically. The results demonstrate that brain
areas supporting conscious vision are not necessary
for remapping, and suggest visual stability is
maintained for salient objects even when they are
not consciously perceived.}
}
@Article{rossion.EA:12,
author = {Bruno Rossion and Esther Alonso Prieto an Adriano
Boremanse and Dana Kuefner and Goedele {Van Belle}},
title = {A steady-state visual evoked potential approach to
individual face perception: Effect of inversion,
contrast-reversal and temporal dynamics},
journal = NI,
year = 2012,
volume = 63,
pages = {1585--1600},
abstract = {Presentation of a face stimulus for several seconds
at a periodic frequency rate leads to a right
occipito-temporal evoked steady-state visual
potential (SSVEP) confined to the stimulation
frequency band. According to recent evidence
(Rossion and Boremanse, 2011), this face-related
SSVEP is largely reduced in amplitude when the exact
same face is repeated at every stimulation cycle as
compared to the presentation of different individual
faces. Here this SSVEP individual face repetition
effect was tested in 20 participants stimulated with
faces at a 4 Hz rate for 84 s, in 4 conditions:
faces upright or inverted, normal or
contrast-reversed (2 × 2 design). To study the
temporal dynamics of this effect, all stimulation
sequences started with 15 s of identical faces,
after which, in half of the sequences, different
faces were introduced. A larger response to
different than identical faces at the fundamental (4
Hz) and second harmonic (8 Hz) components was
observed for upright faces over the right
occipito-temporal cortex. Weaker effects were found
for inverted and contrast-reversed faces, two
stimulus manipulations that are known to greatly
affect the perception of facial identity. Addition
of the two manipulations further decreased the
effect. The phase of the fundamental frequency SSVEP
response was delayed for inverted and
contrast-reversed faces, to the same extent as the
latency delay observed at the peak of the
face-sensitive N170 component observed at
stimulation sequence onset. Time-course analysis of
the entire sequence of stimulation showed an
immediate increase of 4 Hz amplitude at the onset
(16th second) of different face presentation,
indicating a fast, large and frequency-specific
release to individual face adaptation in the human
brain. Altogether, these observations increase our
understanding of the characteristics of the human
steady-state face potential response and provide
further support for the interest of this approach in
the study of the neurofunctional mechanisms of face
perception.}
}
@Article{sahraie.EA:97,
author = {A. Sahraie and L. Weiskrantz and J. L. Barbur and
A. Simmons and S. C. R. Williams and M. J. Brammer},
title = {Pattern of neuronal activity associated with
conscious and unconscious processing of
visual signals},
journal = PNAS,
year = 1997,
volume = 94,
number = 17,
pages = {9406--9411},
abstract = {Following striate cortex damage in monkeys and
humans there can be residual function mediated by
parallel visual pathways. In humans this can
sometimes be associated with a “feeling” that
something has happened, especially with rapid
movement or abrupt onset. For less transient events,
discriminative performance may still be well above
chance even when the subject reports no conscious
awareness of the stimulus. In a previous study we
examined parameters that yield good residual visual
performance in the “blind” hemifield of a subject
with unilateral damage to the primary visual
cortex. With appropriate parameters we demonstrated
good discriminative performance, both with and
without conscious awareness of a visual event. These
observations raise the possibility of imaging the
brain activity generated in the “aware” and the
“unaware” modes, with matched levels of
discrimination performance, and hence of revealing
patterns of brain activation associated with visual
awareness. The intact hemifield also allows a
comparison with normal vision. Here we report the
results of a functional magnetic resonance imaging
study on the same subject carried out under aware
and unaware stimulus conditions. The results point
to a shift in the pattern of activity from neocortex
in the aware mode, to subcortical structures in the
unaware mode. In the aware mode prestriate and
dorsolateral prefrontal cortices (area 46) are
active. In the unaware mode the superior colliculus
is active, together with medial and orbital
prefrontal cortical sites. }
}
@Article{sammer.EA:05,
author = {Gebhard Sammer and Carlo Blecker and Helge Gebhardt
and Peter Kirsch and Rudolf Stark and Dieter Vaitl},
title = {Acquisition of typical {EEG} waveforms during {fMRI:
SSVEP, LRP}, and frontal theta},
journal = NI,
year = 2005,
volume = 24,
pages = {1012--1024},
abstract = {Recent work has demonstrated the feasibility of
simultaneous electro- encephalography (EEG) and
functional magnetic resonance imaging
(fMRI). Virtually no systematic comparisons between
EEG recorded inside and outside the MR scanner have
been conducted, and it is unknown if different kinds
of frequency mix, topography, and domain- specific
processing are uniformly recordable within the
scanner environment. The aim of the study was to
investigate several typical EEG waveforms in the
same subjects inside the magnet during fMRI and
outside the MR examination room. We examined whether
uniform artifact subtraction allows the extraction
of these different EEG waveforms inside the scanner
during EPI scanning to the same extent as outside
the scanner. Three well-established experiments were
conducted, eliciting steady state visual evoked
potentials (SSVEP), lateralized readiness potentials
(LRP), and frontal theta enhancement induced by
mental addition. All waveforms could be extracted
from the EEG recorded during fMRI. Substantially no
differences in these waveforms of interest were
found between gradient-switching and intermediate
epochs during fMRI (only the SSVEP-experiment was
designed for a comparison of gradient—with
intermediate epochs), or between waveforms recorded
inside the scanner during EPI scanning and outside
the MR examination room (all experiments). However,
non-specific amplitude differences were found
between inside and outside recorded EEG at lateral
electrodes, which were not in any interaction with
the effects of interest. The source of these
differences requires further exploration. The high
concordance of activation patterns with published
results demonstrates that EPI-images could be
acquired during EEG recording without significant
distortion.}
}
@Article{sanchezpanchuelo.EA:12,
author = {Rosa M. S{\'a}nchez-Panchuelo and Susan T. Francis
and Denis Schluppeck and Richard W. Bowtell},
title = {Correspondence of Human Visual Areas Identified
Using Functional and Anatomical {MRI} In Vivo at {7
T}},
journal = JMRI,
year = 2012,
volume = 35,
pages = {287--299},
abstract = {Purpose: To study the correspondence of anatomically
and functionally defined visual areas (primary
visual cor- tex, V1, and motion selective area
V5/human MTþ) by using structural magnetic resonance
imaging (MRI) and functional MRI (fMRI) in vivo at 7
T. Materials and Methods: Four subjects
participated in this study. High-resolution (\%0.4 mm
isotropic) anatomi- cal MRI was used to identify
cortical regions based on their distinct cortical
lamination. The optimal contrast for identifying
heavily myelinated layers within gray matter was
quantitatively assessed by comparing T1-weighted
magnetization-prepared rapid gradient echo (MPRAGE)
and T2*-weighted, 3D fast-low angle shot (FLASH)
imaging. Retinotopic mapping was performed using
GE-based fMRI at 1.5 mm isotropic resolution to
identify functional areas. Results: T2*-weighted
FLASH imaging was found to pro- vide a significantly
higher contrast-to-noise ratio, allowing
visualization of the stria of Gennari in every slice
of a vol- ume covering the occipital cortex in each
of the four sub- jects in this study. The
independently derived boundary of V1, identified in
the same subjects using retinotopic mapping by fMRI,
closely matched the border of anatomi- cally defined
striate cortex in the human brain. Evidence of
banding was also found within the functionally
defined V5 area; however, we did not find a good
correlation of this area, or the functionally
identified subregion (MT), with the banded area.
Conclusion: High-resolution T2*-weighted images
acquired at 7 T can be used to identify myelinated
bands within cortical gray matter in reasonable
measurement times. Regions where a myelinated band
was identified show a high degree of overlap with
the functionally defined V1 area.}
}
@Article{savazzi.marzi:02,
author = {Silvia Savazzi and Carlo A. Marzi},
title = {Speeding Up Reaction Time with Invisible Stimuli},
journal = CurrBio,
year = 2002,
volume = 12,
pages = {403--407},
abstract = {Normal subjects react more quickly to a pair of
visual stimuli than to a stimulus alone. This
phenomenon is known as the redundant signal effect
(RSE) [1] and represents an example of divided
visual attention in which signal processing is
carried out in parallel to the advantage of response
speed. A most interesting aspect of this phenomenon
is that it can occur when one stimulus in a pair
cannot be consciously detected because of hemianopia
[2, 3] or unilateral extinction [4] resulting from
brain damage. Here, we report that a similar
dissociation between visual awareness and visually
guided behavior is present in normal subjects who
show an RSE even when the luminance of one of a pair
of stimuli is below detection threshold. The
observed RSE cannot be attributed to probability
sum- mation because it violates Miller’s race
inequality [5] and is likely to be related to neural
summation between supra- and subthreshold
stimuli. Given that a similar implicit RSE is
present in hemispherectomy patients [3], we
hypothesize that the site of this summation might be
the superior colliculus (SC).}
}
@Article{savazzi.EA:07,
author = {Silvia Savazzi and Mara Fabri and Guido Rubboli and
Aldo Paggiand Carlo Alberto Tassinari and Carlo
Alberto Marzi},
title = {Interhemispheric transfer following callosotomy in
humans: Role of the superior colliculus},
journal = {Neuropsychologia},
year = 2007,
volume = 45,
pages = {2417--2427},
abstract = {It is now common knowledge that the total surgical
section of the corpus callosum (CC) and of the other
forebrain commissures prevents interhemispheric
transfer (IT) of a host of mental functions. By
contrast, IT of simple sensorimotor functions,
although severely delayed, is not abolished, and an
important question concerns the pathways subserving
this residual IT. To answer this question we
assessed visuomotor IT in split-brain patients using
the Poffenberger paradigm (PP), that is, a
behavioral paradigm in which simple reaction time
(RT) to visual stimuli presented to the hemifield
ipsilateral to the responding hand is compared to
stimuli presented to the contralateral hemifield, a
condition requiring an IT. We tested the possibility
that the residual IT is mediated by the collicular
commissure interconnecting the two sides of the
superior colliculus (SC). To this purpose, we used
short-wavelength visual stimuli, which in
neurophysiological studies in non-human primates
have been shown to be undetectable by collicular
neurons. We found that, in both totally and
partially callosotomised patients, IT was
considerably longer with S-cone input than with
L-cone input or with achromatic stimuli. This was
not the case in healthy participants in whom IT was
not affected by color. These data clearly show that
the SC plays an important role in IT of sensorimotor
information in the absence of the corpus callosum.}
}
@Article{savoy:05,
author = {Robert L. Savoy},
title = {Experimental design in brain activation {MRI}:
Cautionary tales},
journal = BRB,
year = 2005,
volume = 67,
pages = {361--367},
abstract = {The use of functional magnetic resonance imaging
(fMRI) in cognitive neuroscience has expanded at an
amazing rate in the past 10 years. Current research
includes increasingly subtle and specific attempts
to dissect the cognitive and emotional mechanisms
called into play when humans make decisions. The
present essay will briefly review some of the
general considerations and domains of information
needed when one designs fMRI-based
experiments. However, the main theme will be the
difficulties associated with designing, conducting,
analyzing and interpreting such research. Functional
MRI is an unusually complicated technique, and there
are numerous ways for experiments to go wrong. As
well as demanding exceptional care in maintaining
the quality of one’s own research, this makes the
universal problem of evaluating other peoples’
research particularly challenging.}
}
@Article{savoy:06,
author = {Robert L. Savoy},
title = {Using Small Numbers of Subjects in {fMRI}-Based
Research},
journal = IEEEmb,
year = 2006,
volume = 25,
pages = {52--59},
abstract = {Most discussions of brain activation functional mag-
netic resonance imaging (fMRI) data start with the
analysis of images from a single subject but move
rather quickly to the issues associated with group
comparisons and drawing population
conclusions. There are many technical issues
associated with those group compar- isons that do
not arise, or are very different, for data from a
single subject. In addition, there are contexts
(most notably clinical evaluations) where studying
an individual subject is essential. This article
reviews a number of issues related to the special
features and potentials associated with doing
function- al brain imaging experiments with one or a
small number of subjects. It concludes with the
speculation that, ironically, it may someday turn
out that the information from a few brains,
thoroughly studied, will reveal more about the
universal aspects of human brain function and
organization than the cur- rent torrent of studies
from large collections of brains.}
}
@Article{scarpazza.EA:13,
author = {C. Scarpazza and G. Sartori and M.S. {De Simone} and
A. Mechelli},
title = {When the single matters more than the group: Very
high false positive rates in single case Voxel Based
Morphometry},
journal = NI,
year = 2013,
volume = 70,
pages = {175--188},
abstract = {Voxel Based Morphometry (VBM) studies typically
involve a comparison between groups of individuals;
this ap- proach however does not allow inferences to
be made at the level of the individual. In recent
years, an increasing number of research groups have
attempted to overcome this issue by performing
single case studies, which in- volve the comparison
between a single subject and a control
group. However, the interpretation of the results is
problematic; for instance, any significant
difference might be driven by individual variability
in neuroanatomy rather than the neuropathology of
the disease under investigation, or might represent
a false positive due to the data being sampled from
non-normally distributed populations. The aim of the
present investigation was to empirically estimate
the likelihood of detecting significant differences
in gray matter volume in individuals free from
neurological or psychiatric diagnosis. We compared a
total of 200 single subjects against a group of 16
controls matched for age and gender, using two
independent datasets from the Neuroimaging
Informatics Tools and Resources Clearinghouse. We
report that the chance of detecting a significant
difference in a disease-free individual is much
higher than previously expected; for instance, using
a standard voxel-wise threshold of p b 0.05
(corrected) and an extent threshold of 10 voxels,
the likelihood of a single subject showing at least
one significant difference is as high as 93.5\% for
increases and 71\% for decreases. We also report
that the chance of detecting significant differences
was greatest in frontal and temporal cortices and
lowest in subcortical regions. The chance of
detecting significant differences was inversely
related to the degree of smoothing applied to the
data, and was higher for unmodulated than modulated
data. These results were replicated in the two in-
dependent datasets. By providing an empirical
estimation of the number of significant increases
and decreases to be expected in each cortical and
subcortical region in disease-free individuals, the
present investigation could in- form the
interpretation of future single case VBM studies.}
}
@Article{schmid.EA:13,
author = {Michael C. Schmid and Joscha T. Schmiedt and Andrew
J. Peters2and Richard C. Saunders and Alexander
Maier and David A. Leopold},
title = {Motion-Sensitive Responses in Visual Area {V4} in
the Absence of Primary Visual Cortex},
journal = JoN,
year = 2013,
volume = 33,
number = 48,
pages = {18740--18745},
abstract = {Neurons in cortical ventral-stream area V4 are
thought to contribute to important aspects of visual
processing by integrating information from primary
visual cortex (V1). However, how V4 neurons respond
to visual stimulation after V1 injury remains
unclear: While electrophysiological investigation of
V4 neurons during reversible V1 inactivation
suggests that virtually all responses are eliminated
(Girard et al., 1991), fMRI in humans and monkeys
with permanent lesions shows reliable V1-independent
activity (Baseler et al., 1999; Goebel et al., 2001;
Schmid et al., 2010). To resolve this apparent
discrepancy, we longitudinally assessed neuronal
functions of macaque area V4 using chronically
implanted electrode arrays before and after creating
a permanent aspiration lesion in V1. During the
month after lesioning, we observed weak yet
significant spiking activity in response to stimuli
presented to the lesion-affected part of the visual
field. These V1-independent responses showed
sensitivity for motion and likely reflect the effect
of V1-bypassing geniculate input into extrastriate
areas. }
}
@Article{schmidt.EA:02,
author = {Brandon K. Schmidt and Edward K. Vogel and Geoffrey
F. Woodman and Steven J. Luck},
title = {Voluntary and automatic attentional control of
visual working memory},
journal = PP,
year = 2002,
volume = 64,
number = 5,
pages = {754--763},
abstract = {Previous studies of attention-directing cues have
focused largely on the effects of cuing on
perceptual processes, but cuing may also influence
the transfer of perceptual representations into
visual working memory. In the present study, we
examined this potential role of cues, using both
predictive and nonpredictive cues in the context of
a visual working memory task. Each trial began with
a cue, followed by an array of six colored squares,
a delay interval, and then a probe square presented
at the location of one of the squares in the
previous array. The subjects were required to
indicate whether the color of the probe square was
the same as the color of the square that had
previously been presented at the same
location. Performance on this working memory task
was more accurate when the cued location was probed
than when an uncued location was probed, even when
the cued location was no more likely to be probed
than any of the uncued locations. An additional
experiment using the abrupt-onset paradigm of Yantis
and Jonides (1984) yielded similar results. Thus,
visual transients may automatically influence the
transfer of perceptual representations into visual
working memory.}
}
@Article{schoenfeld.EA:02,
author = {Mircea Ariel Schoenfeld and Toemme Noesselt and
Dorothe Poggel and Claus Tempelmann and Jens-Max
Hopf and Martin G. Woldorff and Hans-Jochen Heinze
and Steven A. Hillyard},
title = {Analysis of pathways mediating preserved vision
after striate cortex lesions},
journal = AN,
year = 2002,
volume = 52,
number = 6,
pages = {814--824},
abstract = {This study investigated the neural substrates of
preserved visual functioning in a patient with
homonymous hemianopsia and Riddoch syndrome after a
posterior cerebral artery stroke affecting the
primary visual cortex (area V1). The limited visual
abilities of this patient included above-chance
verbal reports of movement and color change as well
as discrimination of movement direction in the
hemianopic field. Functional magnetic resonance
imaging showed that motion and color-change stimuli
presented to the hemianopic field produced
activation in several extrastriate areas of the
lesioned hemisphere that were defined using
retinotopic mapping. Magnetoencephalographic
recordings indicated that evoked activity occurred
earlier in the higher-tier visual areas V4/V8 and V5
than in the lower-tier areas V2/V3 adjacent to the
lesion. In addition, the functional magnetic
resonance imaging analysis showed an increased
functional connectivity between areas V4/V8 and V5
of the lesioned hemisphere in comparison with the
same areas in the intact hemisphere during the
presentation of color changes. These results suggest
that visual perception after the V1 lesion in
Riddoch syndrome is mediated by subcortical pathways
that bypass V1 and project first to higher-tier
visual areas V5 and V4/V8 and subsequently to
lower-tier areas V2/V3.}
}
@Article{silvanto:15,
author = {Juha Silvanto},
title = {Why is ``blindsight'' blind? A new perspective on
primary visual cortex, recurrent activity and visual
awareness},
journal = ConscCog,
year = 2015,
volume = 32,
pages = {15--32},
abstract = {The neuropsychological phenomenon of blindsight has
been taken to suggest that the pri- mary visual
cortex (V1) plays a unique role in visual awareness,
and that extrastriate acti- vation needs to be fed
back to V1 in order for the content of that
activation to be consciously perceived. The aim of
this review is to evaluate this theoretical
framework and to revisit its key tenets. Firstly, is
blindsight truly a dissociation of awareness and
visual detection? Secondly, is there sufficient
evidence to rule out the possibility that the loss
of awareness resulting from a V1 lesion simply
reflects reduced extrastriate respon- siveness,
rather than a unique role of V1 in conscious
experience? Evaluation of these argu- ments and the
empirical evidence leads to the conclusion that the
loss of phenomenal awareness in blindsight may not
be due to feedback activity in V1 being the hallmark
awareness. On the basis of existing literature, an
alternative explanation of blindsight is
proposed. In this view, visual awareness is a
‘‘global’’ cognitive function as its hallmark is the
availability of information to a large number of
perceptual and cognitive systems; this requires
inter-areal long-range synchronous oscillatory
activity. For these oscillations to arise, a
specific temporal profile of neuronal activity is
required, which is established through recurrent
feedback activity involving V1 and the extrastriate
cortex. When V1 is lesioned, the loss of recurrent
activity prevents inter-areal networks on the basis
of oscil- latory activity. However, as limited
amount of input can reach extrastriate cortex and
some extrastriate neuronal selectivity is preserved,
computations involving comparison of neural firing
rates within a cortical area remain possible. This
enables ‘‘local’’ read-out from spe- cific brain
regions, allowing for the detection and
discrimination of basic visual attributes. Thus
blindsight is blind due to lack of ‘‘global’’
long-range synchrony, and it functions via ‘‘local’’
neural readout from extrastriate areas.}
}
@Article{silvanto.EA:09,
author = {Juha Silvanto and Vincent Walsh and Alan Cowey},
title = {Abnormal functional connectivity between
ipsilesional {V5/MT+} and contralesional striate
cortex {(V1)} in blindsight},
journal = EBR,
year = 2009,
volume = 193,
number = 4,
pages = {645--650},
abstract = {Damage to the visual cortex can lead to changes in
anatomical connectivity between the remaining
areas. For example, after a unilateral lesion to
striate cortex (V1), an abnormal anatomical pathway
can develop between the lateral geniculate nucleus
of the undamaged hemisphere and the motion area
V5/MT+ in the damaged hemisphere, accompanied by a
hypernormal callosal connection between the area
V5/MT+ of the two hemispheres. Here we investigated,
using transcranial magnetic stimulation (TMS), the
functional significance of these pathways in the
blindsight subject GY, in whom they were first
demonstrated. We show that TMS applied over the
extrastriate area V5/MT+ in GY’s damaged hemisphere
modulates the appearance of phosphenes induced from
V1 in the normal hemisphere. In contrast, in
neurologically normal control subjects, TMS applied
over V5/MT+ never influenced the phosphenes induced
from V1 in the other hemisphere. The findings
indicate an abnormal functional connectivity between
V5/MT in the damaged hemisphere and the early visual
cortex in the normal hemisphere, consistent with
GY’s abnormal anatomical connectivity.}
}
@Article{singh.EA:03,
author = {Manbir Singh and Sungheon Kim and Tae-Seong Kim},
title = {Correlation between {BOLD-fMRI and EEG} signal
changes in response to visual stimulus frequency in
humans},
journal = MRM,
year = 2003,
volume = 49,
pages = {108--114},
abstract = {The correlation between signals acquired using
electroencephalography (EEG) and fMRI was
investigated in humans during visual
stimulation. Evoked potential EEG and BOLD fMRI data
were acquired independently under similar conditions
from eight subjects during stimulation by a
checkerboard flashed at frequencies ranging from
2–12 Hz. The results indicate highly correlated
changes in the strength of the EEG signal averaged
over two occipital electrodes and the BOLD signal
within the occipital lobe as a function of flash
frequency for 7/8 subjects (average linear
correlation coefficient of 0.76). Both signals
peaked at approximately 8 Hz. For one subject the
correlation coefficient was 0.20; the EEG signal
peaked at 6 Hz and the BOLD signal peaked at 10
Hz. Overall, the EEG and BOLD signals, each averaged
over 40-sec stimulation periods, appear to be
coupled linearly during visual stimulation by a
flashing checkerboard.}
}
@Article{skudlarski.EA:99,
author = {Pawel Skudlarski and R. Todd Constable and John
C. Gore},
title = {{ROC} Analysis of Statistical Methods Used in
Functional {MRI}: Individual Subjects},
journal = NI,
year = 1999,
volume = 9,
pages = {311--329},
abstract = {The complicated structure of fMRI signals and asso-
ciated noise sources make it difficult to assess the
validity of various steps involved in the
statistical analysis of brain activation. Most
methods used for fMRI analysis assume that
observations are indepen- dent and that the noise
can be treated as white gauss- ian noise. These
assumptions are usually not true but it is difficult
to assess how severely these assumptions are
violated and what are their practical conse-
quences. In this study a direct comparison is made
between the power of various analytical methods used
to detect activations, without reference to
estimates of statistical significance. The
statistics used in fMRI are treated as metrics
designed to detect activations and are not
interpreted probabilistically. The receiver op-
erator characteristic (ROC) method is used to
compare the efficacy of various steps in calculating
an activa- tion map in the study of a single subject
based on optimizing the ratio of the number of
detected activa- tions to the number of
false-positive findings. The main findings are as
follows: Preprocessing. The removal of intensity
drifts and high-pass filtering applied on the voxel
time-course level is beneficial to the efficacy of
analysis. Temporal normalization of the global image
intensity, smoothing in the temporal domain, and
low- pass filtering do not improve power of
analysis. Choices of statistics. the
cross-correlation coefficient and t -statistic, as
well as nonparametric Mann–Whitney statistics, prove
to be the most effective and are similar in
performance, by our criterion. Task design. the
proper design of task protocols is shown to be
crucial. In an alternating block design the optimal
block length is be approximately 18 s. Spatial
clustering. an initial spatial smoothing of images
is more efficient than cluster filtering of the
statistical parametric activation maps.}
}
@Article{smith.EA:09,
author = {A. T. Smith and P. L. Cotton and A. Bruno and
C. Moutsiana},
title = {Dissociating Vision and Visual Attention in the
Human Pulvinar},
journal = JoNeurophys,
year = 2009,
key = 101,
volume = 2,
pages = {917--925},
abstract = {The pulvinar region of the thalamus has repeatedly
been linked with the control of attention. However,
the functions of the pulvinar remain poorly
characterized, both in human and in nonhuman
primates. In a functional MRI study, we examined the
relative contributions to activity in the human
posterior pulvinar made by visual drive (the
presence of an unattended visual stimulus) and
attention (covert spatial attention to the
stimulus). In an event-related design, large optic
flow stimuli were presented to the left and/or right
of a central fixation point. When unattended, the
stimuli robustly activated two regions of the
pulvinar, one medial and one dorsal with respect to
the lateral geniculate. The activity in both regions
shows a strong contralateral bias, suggesting
retinotopic organization. Primate physiology
suggests that the two regions could be two portions
of the same double map of the visual field. In our
paradigm, attending to the stimulus enhanced the
response by about 20\%. Thus attention is not
necessary to activate the human pulvinar and the
degree of attentional enhancement matches, but does
not exceed, that seen in the cortical regions with
which the posterior pulvinar connects.}
}
@Article{srinivasan.EA:07,
author = {Ramesh Srinivasan and Eleonora Fornari and Maria
G. Knyazeva and Reto Meuli and Philippe Maeder},
title = {{fMRI} responses in medial frontal cortex that
depend on the temporal frequency of visual input},
journal = ExpBrRes,
year = 2007,
volume = 180,
number = 4,
pages = {677--691},
abstract = {Functional networks in the human brain have been
investigated using electrophysiological methods
(EEG/MEG, LFP, and MUA) and steady-state paradigms
that apply periodic luminance or contrast modulation
to drive cortical networks. We have used this
approach with fMRI to characterize a cortical
network driven by a checkerboard reversing at a
fixed frequency. We found that the fMRI signals in
voxels located in occipital cortex were increased by
checkerboard reversal at frequencies ranging from 3
to 14 Hz. In contrast, the response of a cluster of
voxels centered on basal medial frontal cortex
depended strongly on the reversal frequency,
consistently exhibiting a peak in the response for
specific reversal frequencies between 3 and 5 Hz in
each subject. The fMRI signals at the frontal voxels
were positively correlated indicating a homogeneous
cluster. Some of the occipital voxels were
positively correlated to the frontal voxels
apparently forming a large-scale functional
network. Other occipital voxels were negatively
correlated to the frontal voxels, suggesting a
functionally distinct network. The results provide
preliminary fMRI evidence that during visual
stimulation, input frequency can be varied to engage
different functional networks.}
}
@Article{sterzer.kleinschmidt:10,
author = {Philipp Sterzer and Andreas Kleinschmidt},
title = {Anterior insula activations in perceptual paradigms:
often observed but barely understood},
journal = BSF,
year = 2010,
volume = 214,
pages = {611--622},
abstract = {Anterior insular cortex is among the non-sen- sory
brain regions most commonly found activated in
functional brain imaging studies on visual and
auditory perception. However, most of these studies
do not explic- itly address the functional role of
this specific brain region in perception, but rather
report its activation as a by- product. Here, we
attempt to characterize the involvement of anterior
insular cortex in various perceptual paradigms,
including studies of visual awareness, perceptual
decision making, cross-modal sensory processes and
the role of spontaneous neural activity fluctuations
in perception. We conclude that anterior insular
cortex may be associated with perception in that it
underpins heightened alertness of either stimulus-
or task-driven origin, or both. Such a mechanism
could integrate endogenous and exogenous functional
demands under the joint criterion of whether they
challenge an individual’s homeostasis.}
}
@Article{stevens.EA:13,
author = {M. Tynan R. Stevens and Ryan C.N. D'Arcye and
Gerhard Stroink and David B. Clarke and Steven
D. Beyea},
title = {Thresholds in {fMRI} studies: Reliable for single
subjects?},
journal = JNMeth,
year = 2013,
volume = 219,
pages = {312--323},
abstract = {Many studies have investigated test–retest
reliability of active voxel classification for fMRI,
which is increasingly important for emerging
clinical applications. The implicit impact of
voxel-wise thresholding on this type of reliability
has previously been under-appreciated. This has had
two detrimental effects: (1) reliability studies use
different fixed thresholds, making comparison of
results is challenging; (2) typical studies do not
assess reliability at the individual level, which
could provide information for selecting acti- vation
thresholds. To show the limitations of traditional
fixed-threshold approaches, we investigated the
threshold dependence of fMRI reliability measures,
with the goal of developing an automated threshold
selection routine. For this purpose, we demonstrated
threshold dependence of both novel (ROC-reliability
or ROC-r) and established (Rombouts overlap or RR)
reliability measures. Both methods rely minimally on
statistical assumptions, and provide a data-driven
summary of the threshold–reliability
relationship. We applied these methods to data from
eight subjects performing a simple finger tapping
task across repeated fMRI sessions. We showed that
the reliability measures varied dramatically with
threshold. This variation depended strongly on the
individual tested. Finally, we demonstrated novel
procedures using ROC-r and overlap analysis to
optimize thresholds on a case-by-case
basis. Ultimately, a method to determine robust
individual-level activation maps represents a
critical advance for fMRI as a diagnostic tool.}
}
@Article{stoerig.cowey:97,
author = {Petra Stoerig and Alan Cowey},
title = {Blindsight in man and monkey},
journal = {Brain},
year = 1997,
volume = 120,
pages = {535--559},
abstract = {In man and monkey, absolute cortical blindness is
caused by degeneration. While extrastriate cortical
areas participate in the mediation of the
forced-choice responses, a concomitant destruction
of the optic radiations and/or the primary visual
cortex. It is characterized by an absence of any
conscious striate cortical activation does not seem
to be necessary for blindsight. Whether the loss of
phenomenal vision is a vision, but stimuli presented
inside its borders may nevertheless be
processed. This unconscious vision includes
necessary consequnce of striate cortical destruction
and whether this structure is indispensable for
conscious sight neuroendocrine, reflexive, indirect
and forced-choice responses which are mediated by
the visual subsystems are much debated questions
which need to be tackled experimentally.}
}
@Article{stoerig.EA:98,
author = {Petra Stoerig and Andreas Kleinschmidt and Jens
Frahm},
title = {No visual responses in denervated V1:
high-resolution functional magnetic resonance
imaging of a blindsight patient},
journal = {Neuroreport},
year = 1998,
volume = 9,
number = 1,
pages = {21--25},
abstract = {Following severe cranio-cerebral trauma that
affected the optic radiation, patient FS suffers
from an incomplete macula-splitting
hemianopia. Within the hemianopic field, FS exhibits
blindsight, i.e. he detects and discriminates visual
stimuli he cannot (consciously) see. We performed
functional magnetic resonance imaging (fMRI) at high
spatial resolution using a large flickering stimulus
field to assess visual responsiveness of
deafferented V1. Contrasting strong activation of
the normal contralesional visual cortex,
ipsilesional V1 displayed no stimulus-related MRI
signal changes. However, activation was observed in
ipsilesional extrastriate cortex. We conclude that
blindsight does not depend on functional islands of
tissue preserved within the deafferented striate
cortex.}
}
@Article{tinelli.EA:13,
author = {Francesca Tinelli and Guido Marco Cicchini and
Roberto Arrighi and Michela Tosetti and Giovanni
Cioni and Maria Concetta Morrone},
title = {Blindsight in children with congenital and acquired
cerebral lesions},
journal = {Cortex},
year = 2013,
volume = 49,
pages = {1636--1647},
abstract = {It has been shown that unconscious visual function
can survive lesions to optical radia- tions and/or
primary visual cortex (V1), a phenomenon termed
“blindsight”. Studies on animal models (cat and
monkey) show that the age when the lesion occurs
determines the extent of residual visual
capacities. Much less is known about the functional
and under- lying neuronal repercussions of early
cortical damage in humans. We measured sensitivity
to several visual tasks in four children with
congenital unilateral brain lesions that severely
affected optic radiations, and in another group of
three children with similar lesions, acquired in
childhood. In two of the congenital patients, we
measured blood oxygenation level dependent (BOLD)
activity in response to stimulation of each visual
field quadrants. Results show clear evidence of
residual unconscious processing of position,
orientation and motion of visual stimuli displayed
in the scotoma of congenitally lesioned children,
but not in the children with acquired lesions. The
calcarine cortical BOLD responses were abnormally
elicited by stimulation of the ipsilateral visual
field and in the scotoma region, demonstrating a
profound neuronal reorganization. In conclusion, our
data suggest that congenital lesions can trigger
massive reorganization of the visual system to
alleviate functional effects of early brain
insults.}
}
@Article{toffanin.EA:09,
author = {Paolo Toffanin and Ritske {de Jong} and Addie
Johnson and Sander Martens},
title = {Using frequency tagging to quantify attentional
deployment in a visual divided attention task},
journal = IJP,
year = 2009,
volume = 72,
pages = {289--298},
abstract = {Frequency tagging is an EEG method based on the
quantification of the steady state visual evoked
potential (SSVEP) elicited from stimuli which
flicker with a distinctive frequency. Because the
amplitude of the SSVEP is modulated by attention
such that attended stimuli elicit higher SSVEP
amplitudes than do ignored stimuli, the method has
been used to investigate the neural mechanisms of
spatial attention. However, up to now it has not
been shown whether the amplitude of the SSVEP is
sensitive to gradations of attention and there has
been debate about whether attention effects on the
SSVEP are dependent on the tagging frequency
used. We thus compared attention effects on SSVEP
across three attention conditions—focused, divided,
and ignored—with six different tagging
frequencies. Participants performed a visual
detection task (respond to the digit 5 embedded in a
stream of characters). Two stimulus streams, one to
the left and one to the right of fixation, were
displayed simultaneously, each with a background
grey square whose hue was sine-modulated with one of
the six tagging frequencies. At the beginning of
each trial a cue indicated whether targets on the
left, right, or both sides should be responded
to. Accuracy was higher in the focused- than in the
divided- attention condition. SSVEP amplitudes were
greatest in the focused-attention condition,
intermediate in the divided-attention condition, and
smallest in the ignored-attention condition. The
effect of attention on SSVEP amplitude did not
depend on the tagging frequency used. Frequency
tagging appears to be a flexible technique for
studying attention.}
}
@Article{urbanski.EA:14,
author = {Marika Urbanski and Olivier A. Coubard and Cl{\'e}mence
Bourlon},
title = {Visualizing the blind brain: brain imaging of visual
field defects from early recovery to rehabilitation
techniques},
journal = FIN,
year = 2014,
volume = 8,
number = 74,
note = {doi:10.3389/fnint.2014.00074},
abstract = {Visual field defects (VFDs) are one of the most
common consequences observed after brain injury,
especially after a stroke in the posterior cerebral
artery territory. Less frequently, tumors, traumatic
brain injury, brain surgery or demyelination can
also determine various visual disabilities, from a
decrease in visual acuity to cerebral
blindness. Visual field defects is a factor of bad
functional prognosis as it compromises many daily
life activities (e.g., obstacle avoidance, driving,
and reading) and therefore the patient’s quality of
life. Spontaneous recovery seems to be limited and
restricted to the first 6 months, with the best
chance of improvement at 1 month. The possible
mechanisms at work could be partly due to cortical
reorganization in the visual areas (plasticity)
and/or partly to the use of intact alternative
visual routes, first identified in animal studies
and possibly underlying the phenomenon of
blindsight. Despite processes of early recovery,
which is rarely complete, and learning of
compensatory strategies, the patient’s autonomy may
still be compromised at more chronic
stages. Therefore, various rehabilitation therapies
based on neuroanatomical knowledge have been
developed to improve VFDs. These use eye-movement
training techniques (e.g., visual search, saccadic
eye movements), reading training, visual field
restitution (the Vision Restoration Therapy, VRT),
or perceptual learning. In this review, we will
focus on studies of human adults with acquired VFDs,
which have used different imaging techniques
(Positron Emission Tomography, PET; Diffusion Tensor
Imaging, DTI; functional Magnetic Resonance Imaging,
fMRI; Magneto Encephalography, MEG) or
neurostimulation techniques (Transcranial Magnetic
Stimulation, TMS; transcranial Direct Current
Stimulation, tDCS) to show brain activations in the
course of spontaneous recovery or after specific
rehabilitation techniques.}
}
@InCollection{vallar:00,
author = {G. Vallar},
title = {The methodological foundations of human
neuropsychology: studies in brain-damaged patient},
booktitle = {Handbook of neuropsychology},
publisher = {Elsevier},
year = 2000,
editor = {F. Boller and J. Grafman},
volume = 1,
pages = {53--76},
edition = {2nd},
address = {Amsterdam}
}
@Article{vialatte.EA:10,
author = {Fran{\,c}ois-Beno{\^i}t Vialatte and Monique Maurice
and Justin Dauwels and Andrzej Cichocki},
title = {Steady-state visually evoked potentials: Focus on
essential paradigms and future perspectives},
journal = PN,
year = 2010,
volume = 90,
pages = {418--438},
abstract = {After 40 years of investigation, steady-state
visually evoked potentials (SSVEPs) have been shown
to be useful for many paradigms in cognitive (visual
attention, binocular rivalry, working memory, and
brain rhythms) and clinical neuroscience (aging,
neurodegenerative disorders, schizophrenia,
ophthalmic pathologies, migraine, autism,
depression, anxiety, stress, and
epilepsy). Recently, in engineering, SSVEPs found a
novel application for SSVEP-driven brain–computer
interface (BCI) systems. Although some SSVEP
properties are well documented, many questions are
still hotly debated. We provide an overview of
recent SSVEP studies in neuroscience (using
implanted and scalp EEG, fMRI, or PET), with the
perspective of modern theories about the visual
pathway. We investigate the steady-state evoked
activity, its properties, and the mechanisms behind
SSVEP generation. Next, we describe the SSVEP-BCI
paradigm and review recently developed SSVEP-based
BCI systems. Lastly, we outline future research
directions related to basic and applied aspects of
SSVEPs.}
}
@Article{walters.EA:03,
author = {Nathan B. Walters and Gary F. Egan and Jillian
J. Kril and Michael Kean and Patricia Waley and Mark
Jenkinson and John D. G. Watson},
title = {In vivo identification of human cortical areas using
high-resolution {MRI}: An approach to cerebral
structure–function correlation},
journal = PNAS,
year = 2003,
volume = 100,
number = 5,
pages = {2981--2986},
abstract = {Understanding the relationship between the
structural and func- tional organization of the
human brain is one of the most impor- tant goals of
neuroscience. Individual variability in brain
structure means that it is essential to obtain this
information from the same subject. To date, this has
been almost impossible. Even though noninvasive
functional imaging techniques such as functional MRI
(fMRI) are now commonplace, there is no
complementary nonin- vasive structural technique. We
present an in vivo method of examining the detailed
neuroanatomy of any individual, which can then be
correlated with that individual’s own functional
results. This method utilizes high-resolution
structural MRI to identify distinct cortical regions
based on cortical lamination structure. We
demonstrate that the observed MR lamination patterns
relate to myeloarchitecture through a correlation of
histology with MRI. In vivo high-resolution MRI
studies identify striate cortex, as well as visual
area V5, in four individuals, as defined by using
fMRI. The anatomical identification of a cortical
area (V5 MT) outside of striate cortex is a
significant advance, proving it possible to identify
extra-striate cortical areas and demonstrating that
in vivo struc- tural mapping of the human cerebral
cortex is possible.}
}
@Article{wan.EA:06,
author = {Xiaohong Wan and Jorge Riera and Kazuki Iwata and
Makoto Takahashi and Toshio Wakabayashi and Ryuta
Kawashima},
title = {The neural basis of the hemodynamic response
nonlinearity in human primary visual cortex:
Implications for neurovascular coupling mechanism},
journal = NI,
year = 2006,
volume = 32,
number = 2,
pages = {616--625},
abstract = {It has been well recognized that the nonlinear
hemodynamic responses of the blood oxygenation
level-dependent (BOLD) functional MRI (fMRI) are
important and ubiquitous in a series of experimental
paradigms, especially for the event-related
fMRI. Although this phenomenon has been intensively
studied and it has been found that the
post-capillary venous expansion is an intrinsically
nonlinear mechanical process, the existence of an
additional neural basis for the nonlinearity has not
been clearly shown. In this paper, we assessed the
correlation between the electric and vascular
indices by performing simultaneous
electroencephalography (EEG) and fMRI recordings in
humans during a series of visual stimulation (i.e.,
radial checkerboard). With changes of the visual
stimulation frequencies (from 0.5 to 16 Hz) and
contrasts (from 1% to 100%), both the event related
potentials (ERPs) and hemodynamic responses show
nonlinear behaviors. In particular, the mean power
of the brain electric sources and the neuronal
efficacies (as originally defined in the
hemodynamics model [Friston et al. Neuroimage, 12,
466–477, 2000], here represent the vascular inputs)
in primary visual cortex consistently show a linear
correlation for all subjects. This indicates that
the hemodynamic response nonlinearity found in this
paper primarily reflects the nonlinearity of
underlying neural activity. Most importantly, this
finding underpins a nonlinear neurovascular
coupling. Specifically, it is shown that the
transferring function of the neurovascular coupling
is likely a power transducer, which integrates the
fast dynamics of neural activity into the vascular
input of slow hemodynamics.}
}
@Article{weil.EA:09,
author = {R.S. Weil and G.T. Plant and M. James-Galton and
G. Rees},
title = {Neural correlates of hemianopic completion across
the vertical meridian},
journal = {Neuropsychologia},
year = 2009,
volume = 47,
pages = {457--464},
abstract = {Hemianopic completion refers to the perceptual
completion of figures located across the vertical
merid- ian in the context of hemianopia, such that
one half of the figure falls within the blind
hemifield. It can occur whether the figure is itself
complete (veridical completion) or incomplete
(paracompletion). Psy- chophysical evidence suggests
that this phenomenon may be a constructive one, and
may share features with completion phenomena in
normal vision. The neural structures mediating
hemianopic completion are unknown. Here we studied
the neural activity evoked by hemianopic completion
using event-related fMRI in an individual (POV) with
a large right visual field homonymous hemianopic
scotoma due to left occipital damage. Either a large
achromatic circular contour straddling the vertical
meridian or a semi- circular contour within the left
hemifield just crossing the vertical meridian was
presented to POV on each trial. POV indicated by
button press whether he perceived a semicircular
contour, a patchy circular contour or a complete
circular contour. On trials where he reported
perceiving a complete circular contour despite being
presented with a semicircular contour
(paracompletion), activity was increased in a region
of ipsilateral extrastriate cortex (contralateral to
the lesion, ipsilateral to the illusory edge of the
circle). These results are discussed in the context
of illusory contour completion in healthy subjects
and more generally in the recovery of function after
brain damage.}
}
@Article{weiskrantz:96,
author = {Lawrence Weiskrantz},
title = {Blindsight revisited},
journal = CurrOpNeuro,
year = 1996,
volume = 6,
pages = {215--220},
abstract = {Some human patients with lesions to their primary
visual (striate) cortex (V1) demonstrate residual
visual capacity, but without acknowledged perceptual
awareness. This phenomenon has been termed
blindsight. Recent results from work on blindsight
patients suggest that it is unlikely to be
attributable to intact residual areas (tags) of
V1. Previous research has reported that blindsight
patients can retain the ability to detect
monochromatic light and grating stimuli, and to
discriminate orientation and direction of movement
in their 'blind' fields. These findings have been
joined by reports that these patients also are
sensitive to, and are able to discriminate,
wavelength in the absence of any experience of
'colour'. This reveals that retinal pathways other
than those to the striate cortex are crucially
involved in vision. Conditions can be controlled for
obtaining either acknowledged awareness or
unawareness of discrimination of the direction of a
small moving target in blindsight patients. This
potentially offers the possibility to determine
whether there are structures uniquely involved in
visual awareness. Monkeys lacking V1 also clearly
demonstrate residual visual capacity, and some
evidence exists that they also experience
'blindsight'.}
}
@Article{winawer.EA:10,
author = {Jonathan Winawer and Hiroshi Horiguchi and Rory
A. Sayres and Kaoru Amano and Brian A. Wandell},
title = {Mapping {hV4} and ventral occipital cortex: The
venous eclipse},
journal = JoVis,
year = 2010,
volume = 10,
number = 5,
pages = {1--22},
abstract = {While the fourth human visual field map (hV4) has
been studied for two decades, there remain
uncertainties about its spatial organization. In
analyzing fMRI measurements designed to resolve
these issues, we discovered a significant problem
that afflicts measurements from ventral occipital
cortex, and particularly measurements near hV4. In
most hemispheres the fMRI hV4 data are contaminated
by artifacts from the transverse sinus (TS). We
created a model of the TS artifact and showed that
the model predicts the locations of anomalous fMRI
responses to simple large-field on–off stimuli. In
many subjects, and particularly the left hemisphere,
the TS artifact masks fMRI responses specifically in
the region of cortex that distinguishes the two main
hV4 models. By selecting subjects with a TS
displaced from the lateral edge of hV4, we were able
to see around the vein. In these subjects, the
visual field coverage extends to the lower meridian,
or nearly so, consistent with a model in which hV4
is located on the ventral surface and responds to
signals throughout the full contralateral
hemifield.}
}
@Article{wu.EA:10,
author = {Zhenghua Wu and Dezhong Yao and Yu Tang and Yilan
Huang and Sheng Su},
title = {Amplitude modulation of steady-state visual evoked
potentials by event-related potentials in a working
memory task},
journal = JBP,
year = 2010,
volume = 36,
pages = {261--271},
abstract = {Previous studies have shown that the amplitude and
phase of the steady-state visual-evoked potential
(SSVEP) can be influenced by a cognitive task, yet
the mechanism of this influence has not been
understood. As the event-related potential (ERP) is
the direct neural electric response to a cognitive
task, studying the relationship between the SSVEP
and ERP would be meaningful in understanding this
underlying mechanism. In this work, the traditional
average method was applied to extract the ERP
directly, following the stimulus of a working memory
task, while a technique named steady-state probe
topography was utilized to estimate the SSVEP under
the simultaneous stimulus of an 8.3-Hz flicker and a
working memory task; a comparison between the ERP
and SSVEP was completed. The results show that the
ERP can modulate the SSVEP amplitude, and for
regions where both SSVEP and ERP are strong, the
modulation depth is large.}
}
@Article{yan.gao:11,
author = {Zheng Yan and Xiaorong Gao},
title = {Functional connectivity analysis of steady-state
visual evoked potentials},
journal = NeuroLett,
year = 2011,
volume = 499,
pages = {199--203},
abstract = {In this paper, functional connectivity of
steady-state visual evoked potential (SSVEP) was
investigated. Directed transfer function (DTF) was
applied to cortical signals recorded from
electroencephalography (EEG) in order to obtain
connectivity patterns. Flow gain was proposed to
assess the role of the specific brain region
involved in the information transmission process. We
found network connections exist in many regions
beyond occipital region. Flow gain mapping both in
8–12 Hz and 13–30 Hz showed that parietal region
seemed to serve as the sole hub of information
transmission. Further studies of flow gain obtained
from channel Pz showed two distinct peaks centered
at about 12 Hz low frequency and 20 Hz medium
frequency respectively. The low frequency region had
a larger value of flow gain. The present study
introduced functional connectivity into
SSVEP. Furthermore, we put forward the concept of
flow gain for the first time to explore the exchange
and processing of brain information during SSVEP.}
}
@Article{zeki.ffytche:98,
author = {S. Zeki and D. H. ffytche},
title = {The {Riddoch} syndrome: insights into the
neurobiology of conscious vision},
journal = {Brain},
year = 1998,
volume = 121,
pages = {25--45},
annote = {We have studied a patient, G.Y., who was rendered
hemianopic following a lesion affecting the primary
visual cortex (area V1), sustained 31 years ago,
with the hope of characterizing his ability to
discriminate visual stimuli presented in his blind
field, both psychophysically and in terms of the
brain activity revealed by imaging methods. Our
results show that (i) there is a correlation between
G.Y.’s capacity to discriminate stimuli presented in
his blind field and his conscious awareness of the
same stimuli and (ii) that G.Y.’s performance on
some tasks is characterized by a marked variability,
both in terms of his awareness for a given level of
discrimination and in his discrimination for a given
level of awareness. The observations on G.Y., and a
comparison of his capacities with those of normal
subjects, leads us to propose a simple model of the
relationship between visual discrimination and
awareness. This supposes that the two independent
capacities are very tightly coupled in normal
subjects (gnosopsia) and that the effect of a V1
lesion is to uncouple them, but only slightly. This
uncoupling leads to two symmetrical departures, on
the one hand to gnosanopsia (awareness without
discrimination) and on the other to agnosopsia
(discrimination without awareness). Our functional
MRI studies show that V5 is always active when
moving stimuli, whether slow or fast, are presented
to his blind field and that the activity in V5
co-varies with less intense activity in other
cortical areas. The difference in cerebral activity
between gnosopsia and agnosopsia is that, in the
latter, the activity in V5 is less intense and lower
statistical thresholds are required to demonstrate
it. Direct comparison of the brain activity during
individual ‘aware’ and ‘unaware’ trials, corrected
for the confounding effects of motion, has also
allowed us, for the first time, to titrate conscious
awareness against brain activity and show that there
is a straightforward relationship between awareness
and activity, both in individual cortical areas, in
this case area V5, and in the reticular activating
system. The imaging evidence, together with the
variability in his levels of awareness and
discrimination, manifested in his capacity to
discriminate consciously on some occasions and
unconsciously on others, leads us to conclude that
agnosopsia, gnosopsia and gnosanopsia are all
manifestations of a single condition which we call
the Riddoch syndrome, in deference to the British
neurologist who, in 1917, first characterized the
major aspect of this disability. We discuss the
significance of these results in relation to
historical views about the organization of the
visual brain.}
}
@Article{zhang.EA:11,
author = {Peng Zhang and Keith Jamison and Stephen Engel and
Bin He and Sheng He},
title = {Binocular Rivalry Requires Visual Attention},
journal = {Neuron},
year = 2011,
volume = 71,
pages = {362--369},
abstract = {An interocular conflict arises when different images
are presented to each eye at the same spatial loca-
tion. The visual system resolves this conflict
through binocular rivalry: observers consciously
perceive spontaneous alternations between the two
images. Visual attention is generally important for
resolving competition between neural
representations. How- ever, given the seemingly
spontaneous and auto- matic nature of binocular
rivalry, the role of attention in resolving
interocular competition remains unclear. Here we
test whether visual attention is necessary to
produce rivalry. Using an EEG frequency-tagging
method to track cortical representations of the con-
flicting images, we show that when attention was
diverted away, rivalry stopped. The EEG data further
suggested that the neural representations of the di-
choptic images combined without attention. Thus,
attention is necessary for dichoptic images to be
engaged in sustained rivalry and may be generally
required for resolving conflicting, potentially
ambig- uous input and giving a single interpretation
access to consciousness.}
}