Results for ' PRIMARY VISUAL-CORTEX'

986 found
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  1. Primary visual cortex and visual awareness.Frank Tong - 2003 - Nature Reviews Neuroscience 4 (3):219-229.
  2.  61
    The role of primary visual cortex (v1) in visual awareness.Victor A. F. Lamme, H. Landman Super, P. R. R. Roelfsema & H. Spekreijse - 2000 - Vision Research 40 (10):1507-21.
  3.  26
    BOLD Responses in Human Primary Visual Cortex are Insensitive to Substantial Changes in Neural Activity.J. B. Swettenham, S. D. Muthukumaraswamy & K. D. Singh - 2013 - Frontiers in Human Neuroscience 7.
  4.  17
    Spontaneous Activity in Primary Visual Cortex Relates to Visual Creativity.Yibo Wang, Junchao Li, Zengjian Wang, Bishan Liang, Bingqing Jiao, Peng Zhang, Yingying Huang, Hui Yang, Rengui Yu, Sifang Yu, Delong Zhang & Ming Liu - 2021 - Frontiers in Human Neuroscience 15.
    Cognitive and neural processes underlying visual creativity have attracted substantial attention. The current research uses a critical time point analysis to examine how spontaneous activity in the primary visual area is related to visual creativity. We acquired the functional magnetic resonance imaging data of 16 participants at the resting state and during performing a visual creative synthesis task. According to the CTPA, we then classified spontaneous activity in the PVA into critical time points, which reflect (...)
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  5.  57
    Unconscious inference and conscious representation: Why primary visual cortex (v1) is directly involved in visual awareness.Zhicheng Lin - 2008 - Behavioral and Brain Sciences 31 (2):209-210.
    The extent to which visual processing can proceed in the visual hierarchy without awareness determines the magnitude of perceptual delay. Increasing data demonstrate that primary visual cortex (V1) is involved in consciousness, constraining the magnitude of visual delay. This makes it possible that visual delay is actually within the optimal lengths to allow sufficient computation; thus it might be unnecessary to compensate for visual delay.
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  6.  68
    Visually Driven Activation in Macaque Areas V2 and V3 without Input from the Primary Visual Cortex.Michael C. Schmid & Mark A. Augath - unknown
    Creating focal lesions in primary visual cortex (V1) provides an opportunity to study the role of extra-geniculo-striate pathways for activating extrastriate visual cortex. Previous studies have shown that more than 95% of neurons in macaque area V2 and V3 stop firing after reversibly cooling V1 [1,2,3]. However, no studies on long term recovery in areas V2, V3 following permanent V1 lesions have been reported in the macaque. Here we use macaque fMRI to study area V2, (...)
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  7. Colour-constancy mechanisms in primary visual cortex.T. Wachtler - 1996 - In Enrique Villanueva, Perception. Ridgeview Pub. Co. pp. 25-25.
  8.  74
    On the relationship between interocular suppression in the primary visual cortex and binocular rivalry.Sengpiel Frank, Bonhoeffer Tobias, C. B. Freeman Tobe & Blakemore Colin - 2001 - Brain and Mind 2 (1):39-54.
    Both classical psychophysical work and recentfunctional imaging studies have suggested acritical role for the primary visual cortex(V1) in resolving the perceptual ambiguitiesexperienced during binocular rivalry. Here weexamine, by means of single-cell recordings andoptical imaging of intrinsic signals, thespatial characteristics of suppression elicitedby rival stimuli in cat V1. We find that the interocular suppression field of V1 neuronsis centred on the same position in space and isslightly larger (by a factor of 1.3) than theminimum response field, measured through (...)
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  9.  17
    Semantic Grounding of Novel Spoken Words in the Primary Visual Cortex.Max Garagnani, Evgeniya Kirilina & Friedemann Pulvermüller - 2021 - Frontiers in Human Neuroscience 15.
    Embodied theories of grounded semantics postulate that, when word meaning is first acquired, a link is established between symbol and corresponding semantic information present in modality-specific—including primary—sensorimotor cortices of the brain. Direct experimental evidence documenting the emergence of such a link, however, is still missing. Here, we present new neuroimaging results that provide such evidence. We taught participants aspects of the referential meaning of previously unknown, senseless novel spoken words by associating them with either a familiar action or a (...)
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  10. Are we aware of neural activity in primary visual cortex.Francis Crick & Christof Koch - 1995 - Nature 375:121-23.
  11.  48
    Low-level phenomenal vision despite unilateral destruction of primary visual cortex.Petra Stoerig & Erhardt Barth - 2001 - Consciousness and Cognition 10 (4):574-587.
    GY, an extensively studied human hemianope, is aware of salient visual events in his cortically blind field but does not call this ''vision.'' To learn whether he has low-level conscious visual sensations or whether instead he has gained conscious knowledge about, or access to, visual information that does not produce a conscious phenomenal sensation, we attempted to image process a stimulus s presented to the impaired field so that when the transformed stimulus T(s) was presented to the (...)
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  12.  67
    Why is “blindsight” blind? A new perspective on primary visual cortex, recurrent activity and visual awareness.Juha Silvanto - 2015 - Consciousness and Cognition 32:15-32.
  13.  47
    Contributions of cortical feedback to sensory processing in primary visual cortex.Lucy S. Petro, Luca Vizioli & Lars Muckli - 2014 - Frontiers in Psychology 5.
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  14.  22
    Intracranial spectral amplitude dynamics of perceptual suppression in fronto-insular, occipito-temporal, and primary visual cortex.Juan R. Vidal, Marcela Perrone-Bertolotti, Philippe Kahane & Jean-Philippe Lachaux - 2014 - Frontiers in Psychology 5.
  15.  64
    Orientation-specific surround suppression in the primary visual cortex varies as a function of autistic tendency.Anastasia V. Flevaris & Scott O. Murray - 2014 - Frontiers in Human Neuroscience 8.
  16.  39
    Optical images of visible and invisible percepts in the primary visual cortex of primates.Stephen L. Macknik & Michael M. Haglund - 1999 - Proceedings of the National Academy of Sciences of the United States of America 96 (26):15208-15210.
  17.  30
    Blindsight in rodents: The use of a "high-level" distance cue in gerbils with lesions of primary visual cortex.D. P. Carey, Melvyn A. Goodale & E. G. Sprowl - 1990 - Behavioural Brain Research 38:283-289.
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  18.  48
    Audiovisual Association Learning in the Absence of Primary Visual Cortex.Mehrdad Seirafi, Peter De Weerd, Alan J. Pegna & Beatrice de Gelder - 2015 - Frontiers in Human Neuroscience 9.
  19.  41
    Altered Brain Structure and Functional Connectivity of Primary Visual Cortex in Optic Neuritis.Jing Huang, Yunyun Duan, Sidong Liu, Peipeng Liang, Zhuoqiong Ren, Yang Gao, Yaou Liu, Xiaojun Zhang, Jie Lu & Kuncheng Li - 2018 - Frontiers in Human Neuroscience 12.
  20.  25
    Why do stationary visual transients apparently fail to elicit phenomenal vision after unilateral destruction of primary visual cortex?Robert W. Kentridge - 2001 - Consciousness and Cognition 10 (4):588-590.
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  21. Frank sengpiel, tobe cb Freeman, Tobias bonhoef-fer and Colin blakemore/on the relationship between interocular suppression in the primary visual cortex and binocular rivalry 39–54 Frank tong/competing theories of binocular rivalry: A possible. [REVIEW]Perceptual Rivalry Alternations, Robert P. O’Shea & Paul M. Corballis - 2001 - Brain and Mind 2:361-363.
     
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  22.  37
    Models of the Visual Cortex.David Rose & Vernon G. Dobson (eds.) - 1985 - New York: Wiley.
    A comprehensive and stimulating study which presents the views of 71 leading theorists on the underlying mechanisms and functions of the primary visual cortex.
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  23.  45
    Enhanced peripheral visual processing in congenitally deaf humans is supported by multiple brain regions, including primary auditory cortex.Gregory D. Scott, Christina M. Karns, Mark W. Dow, Courtney Stevens & Helen J. Neville - 2014 - Frontiers in Human Neuroscience 8.
  24.  22
    Excitability of the Ipsilateral Primary Motor Cortex During Unilateral Goal-Directed Movement.Takuya Matsumoto, Tatsunori Watanabe, Takayuki Kuwabara, Keisuke Yunoki, Xiaoxiao Chen, Nami Kubo & Hikari Kirimoto - 2021 - Frontiers in Human Neuroscience 15.
    IntroductionPrevious transcranial magnetic stimulation studies have revealed that the activity of the primary motor cortex ipsilateral to an active hand plays an important role in motor control. The aim of this study was to investigate whether the ipsi-M1 excitability would be influenced by goal-directed movement and laterality during unilateral finger movements.MethodTen healthy right-handed subjects performed four finger tapping tasks with the index finger: simple tapping task, Real-word task, Pseudoword task, and Visually guided tapping task. In the Tap task, (...)
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  25.  73
    Mechanisms of Visual Perceptual Learning in Macaque Visual Cortex.Rufin Vogels - 2010 - Topics in Cognitive Science 2 (2):239-250.
    The neural mechanisms underlying behavioral improvement in the detection or discrimination of visual stimuli following learning are still ill understood. Studies in nonhuman primates have shown relatively small and, across studies, variable effects of fine discrimination learning in primary visual cortex when tested outside the context of the learned task. At later stages, such as extrastriate area V4, extensive practice in fine discrimination produces more consistent effects upon responses and neural tuning. In V1 and V4, the (...)
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  26.  95
    Fast backprojections from the motion to the primary visual area necessary for visual awareness.Alvaro Pascual-Leone & Vincent Walsh - 2001 - Science 292 (5516):510-512.
  27.  76
    Thalamocortical dysfunction and complex visual hallucinations in brain disease – are the primary disturbances in the cerebral cortex?Daniel Collerton & Elaine Perry - 2004 - Behavioral and Brain Sciences 27 (6):789-790.
    Applying Behrendt & Young's (B&Y's) model of thalamocortical synchrony to complex visual hallucinations in neurodegenerative disorders, such as dementia with Lewy bodies and progressive supranuclear palsy, leads us to propose that the primary pathology may be cortical rather than thalamic. Additionally, the extinction of active hallucinations by eye closure challenges their conception of the role of reduced sensory input.
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  28. Untying the knot: imagination, perception and their neural substrates.Dan Cavedon-Taylor - 2021 - Synthese 199 (3-4):7203-7230.
    How tight is the conceptual connection between imagination and perception? A number of philosophers, from the early moderns to present-day predictive processing theorists, tie the knot as tightly as they can, claiming that states of the imagination, i.e. mental imagery, are a proper subset of perceptual experience. This paper labels such a view ‘perceptualism’ about the imagination and supplies new arguments against it. The arguments are based on high-level perceptual content and, distinctly, cognitive penetration. The paper also defuses a recent, (...)
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  29. A Linked Aggregate Code for Processing Faces (Revised Version).Michael J. Lyons & Kazunori Morikawa - 2000 - Pragmatics and Cognition 8 (1):63-81.
    A model of face representation, inspired by the biology of the visual system, is compared to experimental data on the perception of facial similarity. The face representation model uses aggregate primary visual cortex (V1) cell responses topographically linked to a grid covering the face, allowing comparison of shape and texture at corresponding points in two facial images. When a set of relatively similar faces was used as stimuli, this Linked Aggregate Code (LAC) predicted human performance in (...)
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  30. Functional Imaging Reveals Visual Modulation of Specific Fields in Auditory Cortex.Mark Augath - unknown
    Merging the information from different senses is essential for successful interaction with real-life situations. Indeed, sensory integration can reduce perceptual ambiguity, speed reactions, or change the qualitative sensory experience. It is widely held that integration occurs at later processing stages and mostly in higher association cortices; however, recent studies suggest that sensory convergence can occur in primary sensory cortex. A good model for early convergence proved to be the auditory cortex, which can be modulated by visual (...)
     
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  31.  19
    Visual P2p component responds to perceived numerosity.Paolo A. Grasso, Irene Petrizzo, Camilla Caponi, Giovanni Anobile & Roberto Arrighi - 2022 - Frontiers in Human Neuroscience 16:1014703.
    Numerosity perception is a key ability for human and non-human species, probably mediated by dedicated brain mechanisms. Electrophysiological studies revealed the existence of both early and mid-latency components of the Electrophysiological (EEG) signal sensitive to numerosity changes. However, it is still unknown whether these components respond to physical or perceived variation in numerical attributes. We here tackled this point by recording electrophysiological signal while participants performed a numerosity adaptation task, a robust psychophysical method yielding changes in perceived numerosity judgments despite (...)
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  32.  71
    The status of blindsight: Near-threshold vision, islands of cortex and the riddoch phenomenon.Robert W. Kentridge & Charles A. Heywood - 1999 - Journal of Consciousness Studies 6 (5):3-11.
    In this introductory paper, we assess the current status of blindsight -- the phenomenon in which patients with damage to their primary visual cortex retain the ability to detect, discriminate and localize visual stimuli presented in areas of their visual field in which they report that they are subjectively blind. Blindsight has garnered a great deal of interest and critical research, in part because of its important implications for the philosophy of mind. We briefly consider (...)
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  33. Implicit biases in visually guided action.Berit Brogaard - 2020 - Synthese 198 (17):S3943–S3967.
    For almost half a century dual-stream advocates have vigorously defended the view that there are two functionally specialized cortical streams of visual processing originating in the primary visual cortex: a ventral, perception-related ‘conscious’ stream and a dorsal, action-related ‘unconscious’ stream. They furthermore maintain that the perceptual and memory systems in the ventral stream are relatively shielded from the action system in the dorsal stream. In recent years, this view has come under scrutiny. Evidence points to two (...)
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  34.  68
    Grasping spatial relationships: Failure to demonstrate allocentric visual coding in a patient with visual form agnosia.H. Chris Dijkerman, A. David Milner & David P. Carey - 1998 - Consciousness and Cognition 7 (3):424-437.
    The cortical visual mechanisms involved in processing spatial relationships remain subject to debate. According to one current view, the ''dorsal stream'' of visual areas, emanating from primary visual cortex and culminating in the posterior parietal cortex, mediates this aspect of visual processing. More recently, others have argued that while the dorsal stream provides egocentric coding of visual location for motor control, the separate ''ventral'' stream is needed for allocentric spatial coding. We have (...)
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  35.  25
    The Predictive Values of Changes in Local and Remote Brain Functional Connectivity in Primary Angle-Closure Glaucoma Patients According to Support Vector Machine Analysis.Qiang Fu, Hui Liu & Yu Lin Zhong - 2022 - Frontiers in Human Neuroscience 16.
    PurposeThe primary angle-closure glaucoma is an irreversible blinding eye disease in the world. Previous neuroimaging studies demonstrated that PACG patients were associated with cerebral changes. However, the effect of optic atrophy on local and remote brain functional connectivity in PACG patients remains unknown.Materials and MethodsIn total, 23 patients with PACG and 23 well-matched Health Controls were enrolled in our study and underwent resting-state functional magnetic resonance imaging scanning. The regional homogeneity method and functional connectivity method were used to evaluate (...)
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  36. Computational implications of gestalt theory: The role of feedback in visual processing.Steven Lehar - 2002
    Neurophysiological investigations of the visual system by way of single-cell recordings have revealed a hierarchical architecture in which lower level areas, such as the primary visual cortex, contain cells that respond to simple features, while higher level areas contain cells that respond to higher order features apparently composed of combinations of lower level features. This architecture seems to suggest a feed-forward processing strategy in which visual information progresses from lower to higher visual areas. However (...)
     
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  37.  29
    Conscious and veridical motion perception in a human hemianope.A. B. Morland - 1999 - Journal of Consciousness Studies 6 (5):43-53.
    Following lesions to the primary visual cortex, some patients maintain visual capacities within areas of the visual field in which they are defined as clinically blind by static field perimetry. Blindsight describes the ability to discriminate visual stimuli in the absence of awareness of the stimuli in such patients. Some patients exhibit blindsight, but others are aware of the stimuli with which they are presented, a response mode that has been referred to as residual (...)
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  38. Cognitive Penetration, Perceptual Learning and Neural Plasticity.Ariel S. Cecchi - 2014 - Dialectica 68 (1):63-95.
    Cognitive penetration of perception, broadly understood, is the influence that the cognitive system has on a perceptual system. The paper shows a form of cognitive penetration in the visual system which I call ‘architectural’. Architectural cognitive penetration is the process whereby the behaviour or the structure of the perceptual system is influenced by the cognitive system, which consequently may have an impact on the content of the perceptual experience. I scrutinize a study in perceptual learning that provides empirical evidence (...)
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  39.  41
    Divisions within the posterior parietal cortex help touch meet vision.Catherine L. Reed - 2007 - Behavioral and Brain Sciences 30 (2):218-218.
    The parietal cortex is divided into two major functional regions: the anterior parietal cortex that includes primary somatosensory cortex, and the posterior parietal cortex (PPC) that includes the rest of the parietal lobe. The PPC contains multiple representations of space. In Dijkerman & de Haan's (D&dH's) model, higher spatial representations are separate from PPC functions. This model should be developed further so that the functions of the somatosensory system are integrated with specific functions within the (...)
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  40.  21
    Effects of three-dimension movie visual fatigue on cognitive performance and brain activity.Ryota Akagi, Hiroki Sato, Tatsuya Hirayama, Kosuke Hirata, Masahiro Kokubu & Soichi Ando - 2022 - Frontiers in Human Neuroscience 16:974406.
    To further develop three-dimensional (3D) applications, it is important to elucidate the negative effects of 3D applications on the human body and mind. Thus, this study investigated differences in the effects of visual fatigue on cognition and brain activity using visual and auditory tasks induced by watching a 1-h movie in two dimensions (2D) and 3D. Eighteen young men participated in this study. Two conditions were randomly performed for each participant on different days, namely, watching the 1-h movie (...)
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  41.  23
    Extrastriate activity reflects the absence of local retinal input.Poutasi W. B. Urale, Lydia Zhu, Roberta Gough, Derek Arnold & Dietrich Samuel Schwarzkopf - 2023 - Consciousness and Cognition 114 (C):103566.
    The physiological blind spot corresponds to the optic disc where the retina contains no light-detecting photoreceptor cells. Our perception seemingly fills in this gap in input. Here we suggest that rather than an active process, such perceptual filling-in could instead be a consequence of the integration of visual inputs at higher stages of processing discounting the local absence of retinal input. Using functional brain imaging, we resolved the retinotopic representation of the physiological blind spot in early human visual (...)
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  42.  18
    A statistical approach for segregating cognitive task stages from multivariate fMRI BOLD time series.Charmaine Demanuele, Florian Bähner, Michael M. Plichta, Peter Kirsch, Heike Tost, Andreas Meyer-Lindenberg & Daniel Durstewitz - 2015 - Frontiers in Human Neuroscience 9:156792.
    Multivariate pattern analysis can reveal new information from neuroimaging data to illuminate human cognition and its disturbances. Here, we develop a methodological approach, based on multivariate statistical/machine learning and time series analysis, to discern cognitive processing stages from functional magnetic resonance imaging (fMRI) blood oxygenation level dependent (BOLD) time series. We apply this method to data recorded from a group of healthy adults whilst performing a virtual reality version of the delayed win-shift radial arm maze (RAM) task. This task has (...)
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  43.  31
    What if worms were sentient? Insights into subjective experience from the Caenorhabditis elegans connectome.Oressia Zalucki, Deborah J. Brown & Brian Key - 2023 - Biology and Philosophy 38 (5):1-25.
    Deciphering the neural basis of subjective experience remains one of the great challenges in the natural sciences. The structural complexity and the limitations around invasive experimental manipulations of the human brain have impeded progress towards this goal. While animals cannot directly report first-person subjective experiences, their ability to exhibit flexible behaviours such as motivational trade-offs are generally considered evidence of sentience. The worm _Caenorhabditis elegans_ affords the unique opportunity to describe the circuitry underlying subjective experience at a single cell level (...)
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  44.  15
    Individual Optimal Attentional Strategy in Motor Learning Tasks Characterized by Steady-State Somatosensory and Visual Evoked Potentials.Takeshi Sakurada, Masataka Yoshida & Kiyoshi Nagai - 2022 - Frontiers in Human Neuroscience 15.
    Focus of attention is one of the most influential factors facilitating motor performance. Previous evidence supports that the external focus strategy, which directs attention to movement outcomes, is associated with better motor performance than the internal focus strategy, which directs attention to body movements. However, recent studies have reported that the EF strategy is not effective for some individuals. Furthermore, neuroimaging studies have demonstrated that the frontal and parietal areas characterize individual optimal attentional strategies for motor tasks. However, whether the (...)
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  45. Blindsight in Monkeys: Lost and (perhaps) found.Sean Allen-Hermanson - 2010 - Journal of Consciousness Studies 17 (1-2): 47-71.
    Stoerig and Cowey’s work is widely regarded as showing that monkeys with lesions in the primary visual cortex have blindsight. However, Mole and Kelly persuasively argue that the experimental results are compatible with an alternative hypothesis positing only a deficit in attention and perceptual working memory. I describe a revised procedure which can distinguish these hypotheses, and offer reasons for thinking that the blindsight hypothesis provides a superior explanation. The study of blindsight might contribute towards a general (...)
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  46.  23
    The Effects of Priming Intermittent Theta Burst Stimulation on Movement-Related and Mirror Visual Feedback-Induced Sensorimotor Desynchronization.Jack Jiaqi Zhang & Kenneth N. K. Fong - 2021 - Frontiers in Human Neuroscience 15.
    The potential benefits of priming intermittent theta burst stimulation with continuous theta burst stimulation have not been examined in regard to sensorimotor oscillatory activities recorded in electroencephalography. The objective of this study was to investigate the modulatory effect of priming iTBS delivered to the motor cortex on movement-related and mirror visual feedback -induced sensorimotor event-related desynchronization, compared with iTBS alone, on healthy adults. Twenty participants were randomly allocated into Group 1: priming iTBS—cTBS followed by iTBS, and Group 2: (...)
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  47.  49
    Effects of unseen stimuli on reaction times to seen stimuli in monkeys with blindsight.Alan Cowey, Petra Stoerig & Carolyne Le Mare - 1998 - Consciousness and Cognition 7 (3):312-323.
    In three macaque monkeys with unilateral removal of primary visual cortex and in one unoperated monkey, we measured reaction times to a visual target that was presented at a lateral eccentricity of 20o in the normal, left, visual hemifield. When an additional stimulus was presented at the corresponding position in the right hemifield (hemianopic in three of the monkeys), it significantly slowed the reaction time to the left target if it preceded it by delays from (...)
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  48.  48
    Mental imagery during sleep.Claude Gottesmann - 2002 - Behavioral and Brain Sciences 25 (2):193-193.
    The descriptive “null” hypothesis is strengthened by the fact that during dreaming sleep stage, the primary visual cortex is deactivated as compared with other sleep stages.
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  49. By.Christof Koch - unknown
    What is the relationship between a visual percept and the underlying neuronal activity in parts of the brain? This manifesto reviews the theoretical framework of Crick and Kochfor answering these questions based on the neuroanatomy and physiology of mammalian cortex and associated subcortical structures. This evidence suggests that primates are not directly aware of neural activity in primary visual cortex, although they may be aware of such activity in extrastriate cortical areas. Psychophysical evidence in humans (...)
     
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  50.  57
    Pictures, propositions, and primitives in the head.Anjan Chatterjee - 2002 - Behavioral and Brain Sciences 25 (2):186-187.
    Data from neuropsychology do not support the idea that the primary visual cortex necessarily displays internal visual images. However, the choice of formats used in human cognition is not restricted to depictive or descriptive representations. Nestled between pictures and propositions, primitive spatial schemas with simple analog features extracted from pictorial scenes may play a subtle but wide role in cognition.
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