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Journal articles on the topic 'Visual pathways'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Bilaniuk, Larissa T., Robert A. Zimmerman, and Peter J. Savino. "VISUAL PATHWAYS." Neuroimaging Clinics of North America 3, no. 1 (1993): 71–83. https://doi.org/10.1016/s1052-5149(25)00143-1.

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2

Eustace, Peter. "Retrochiasmal visual pathways." Current Opinion in Ophthalmology 1, no. 5 (1990): 447–52. http://dx.doi.org/10.1097/00055735-199001050-00004.

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3

Eustace, Peter. "Retrochiasmal visual pathways." Current Opinion in Ophthalmology 1, no. 5 (1990): 447–52. http://dx.doi.org/10.1097/00055735-199010000-00004.

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4

Casagrande, V. "Evolution of visual pathways." Journal of Vision 5, no. 12 (2005): 32. http://dx.doi.org/10.1167/5.12.32.

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5

Sadun, Alfredo A., and Richard M. Rubin. "The Anterior Visual Pathways." Journal of Neuro-Ophthalmology 16, no. 2 (1996): 137–51. http://dx.doi.org/10.1097/00041327-199606000-00011.

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6

Dräger, Ursula C. "Albinism and Visual Pathways." New England Journal of Medicine 314, no. 25 (1986): 1636–38. http://dx.doi.org/10.1056/nejm198606193142508.

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7

SIBTAIN, N. "Imaging posterior visual pathways." Acta Ophthalmologica 86 (September 4, 2008): 0. http://dx.doi.org/10.1111/j.1755-3768.2008.3332.x.

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8

MADRID, M., and M. A. CROGNALE. "Long-term maturation of visual pathways." Visual Neuroscience 17, no. 6 (2000): 831–37. http://dx.doi.org/10.1017/s0952523800176023.

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Previous research in adults has demonstrated the utility of the visual evoked potential (VEP) to measure the integrity of the chromatic and achromatic visual pathways. The VEP has also been shown to be a valuable indicator of maturation of these pathways in infants up to 1 year of age. The present manuscript reports changes in the visual pathways from 2 years to adulthood as measured by the spatio-chromatic VEP. The responses to achromatic reversal stimuli designed to preferentially activate the low spatial-frequency achromatic (luminance) pathways appear adult-like by 1 year of age. The respo

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9

Kovacs-Balint, Z., E. Feczko, M. Pincus, et al. "Early Developmental Trajectories of Functional Connectivity Along the Visual Pathways in Rhesus Monkeys." Cerebral Cortex 29, no. 8 (2018): 3514–26. http://dx.doi.org/10.1093/cercor/bhy222.

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Abstract Early social interactions shape the development of social behavior, although the critical periods or the underlying neurodevelopmental processes are not completely understood. Here, we studied the developmental changes in neural pathways underlying visual social engagement in the translational rhesus monkey model. Changes in functional connectivity (FC) along the ventral object and motion pathways and the dorsal attention/visuo-spatial pathways were studied longitudinally using resting-state functional MRI in infant rhesus monkeys, from birth through early weaning (3 months), given th

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10

Edwards, Mark, Stephanie C. Goodhew, and David R. Badcock. "Using perceptual tasks to selectively measure magnocellular and parvocellular performance: Rationale and a user’s guide." Psychonomic Bulletin & Review 28, no. 4 (2021): 1029–50. http://dx.doi.org/10.3758/s13423-020-01874-w.

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AbstractThe visual system uses parallel pathways to process information. However, an ongoing debate centers on the extent to which the pathways from the retina, via the Lateral Geniculate nucleus to the visual cortex, process distinct aspects of the visual scene and, if they do, can stimuli in the laboratory be used to selectively drive them. These questions are important for a number of reasons, including that some pathologies are thought to be associated with impaired functioning of one of these pathways and certain cognitive functions have been preferentially linked to specific pathways. He

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11

SHATZ, C. J. "Visual Neurobiology: Development of Visual Pathways in Mammals." Science 228, no. 4695 (1985): 67–68. http://dx.doi.org/10.1126/science.228.4695.67.

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12

Kaposvári, Péter, Gergő Csete, Anna Bognár, et al. "Audio–visual integration through the parallel visual pathways." Brain Research 1624 (October 2015): 71–77. http://dx.doi.org/10.1016/j.brainres.2015.06.036.

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13

Sumner, Petroc, Parashkev Nachev, Sarah Castor-Perry, Heather Isenman, and Christopher Kennard. "Which Visual Pathways Cause Fixation-Related Inhibition?" Journal of Neurophysiology 95, no. 3 (2006): 1527–36. http://dx.doi.org/10.1152/jn.00781.2005.

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Visual stimuli can both inhibit and activate motor mechanisms. In one well-known example, the latency of saccadic eye movements is prolonged in the presence of a fixation stimulus, relative to the case in which the fixation stimulus disappears before the target appears. This automatic sensory-motor effect, known as the gap effect or fixation-offset effect, has been associated with inhibitory connections within the superior colliculus (SC). Visual information is provided to the SC and other oculomotor areas, such as the frontal eye fields (FEF), mainly by the magnocellular geniculostriate pathw

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14

De Moraes, Carlos Gustavo. "Anatomy of the Visual Pathways." Journal of Glaucoma 22 (2013): S2—S7. http://dx.doi.org/10.1097/ijg.0b013e3182934978.

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15

Crish, Samuel D., and David J. Calkins. "Central Visual Pathways in Glaucoma." Journal of Neuro-Ophthalmology 35 (September 2015): S29—S37. http://dx.doi.org/10.1097/wno.0000000000000291.

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16

Vidyasagar, T. R. "Eyeing visual pathways in dyslexia." Science 345, no. 6196 (2014): 524. http://dx.doi.org/10.1126/science.345.6196.524-a.

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17

Leruez, S., P. Amati-Bonneau, C. Verny, et al. "Mitochondrial dysfunction affecting visual pathways." Revue Neurologique 170, no. 5 (2014): 344–54. http://dx.doi.org/10.1016/j.neurol.2014.03.009.

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18

Schreiber, Falk. "Visual comparison of metabolic pathways." Journal of Visual Languages & Computing 14, no. 4 (2003): 327–40. http://dx.doi.org/10.1016/s1045-926x(03)00030-2.

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19

Murcia-Belmonte, Verónica, and Lynda Erskine. "Wiring the Binocular Visual Pathways." International Journal of Molecular Sciences 20, no. 13 (2019): 3282. http://dx.doi.org/10.3390/ijms20133282.

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Retinal ganglion cells (RGCs) extend axons out of the retina to transmit visual information to the brain. These connections are established during development through the navigation of RGC axons along a relatively long, stereotypical pathway. RGC axons exit the eye at the optic disc and extend along the optic nerves to the ventral midline of the brain, where the two nerves meet to form the optic chiasm. In animals with binocular vision, the axons face a choice at the optic chiasm—to cross the midline and project to targets on the contralateral side of the brain, or avoid crossing the midline a

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20

LI, ZHENG, and KATHERINE V. FITE. "GABAergic visual pathways in the frog Rana pipiens." Visual Neuroscience 18, no. 3 (2001): 457–64. http://dx.doi.org/10.1017/s0952523801183124.

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Gamma-aminobutyric acid (GABA) is the most prevalent inhibitory neurotransmitter in the vertebrate brain. It can exert its influence either as GABAergic projection pathways or as local interneurons, which play an essential role in many visual functions. However, no GABAergic visual pathways have been studied in frogs so far. In the present study, GABAergic pathways in the central visual system of Rana pipiens were investigated with double-labeling techniques, combining immunocytochemistry for GABA with Rhodamine microspheres for retrograde tracing. Three GABAergic visual pathways were identifi

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21

Zhuang, Xiaohua, Tam Tran, Doris Jin, Riya Philip, and Chaorong Wu. "Aging effects on contrast sensitivity in visual pathways: A pilot study on flicker adaptation." PLOS ONE 16, no. 12 (2021): e0261927. http://dx.doi.org/10.1371/journal.pone.0261927.

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Contrast sensitivity is reduced in older adults and is often measured at an overall perceptual level. Recent human psychophysical studies have provided paradigms to measure contrast sensitivity independently in the magnocellular (MC) and parvocellular (PC) visual pathways and have reported desensitization in the MC pathway after flicker adaptation. The current study investigates the influence of aging on contrast sensitivity and on the desensitization effect in the two visual pathways. The steady- and pulsed-pedestal paradigms were used to measure contrast sensitivity under two adaptation cond

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22

Jaekl, Philip, Alexis Pérez-Bellido, and Salvador Soto-Faraco. "On the ‘visual’ in ‘audio-visual integration’: a hypothesis concerning visual pathways." Experimental Brain Research 232, no. 6 (2014): 1631–38. http://dx.doi.org/10.1007/s00221-014-3927-8.

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23

Clarke, Stephanie. "Vision et langage: quelle importance du traitement en parallèle?" Travaux neuchâtelois de linguistique, no. 33 (December 1, 2000): 67–81. http://dx.doi.org/10.26034/tranel.2000.2681.

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The visual system of man and of non-human primates is organised in a way which favours parallel processing. Different aspects of visual information, such as colour, shape or motion are processed independantly. Focal hemispheric lesions can thus cause very selective deficits. The parvo- and magnocellular pathways, specialised in the processing of psychophysically different visual stimuli, have separate representations at the cortical level. Two main pathways are involved in visual recognition and in visuo-spatial functions respectively. Lesions that occur in the adult and remain restricted to o

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24

Nakano, Tamami, and Kazuko Nakatani. "Cortical networks for face perception in two-month-old infants." Proceedings of the Royal Society B: Biological Sciences 281, no. 1793 (2014): 20141468. http://dx.doi.org/10.1098/rspb.2014.1468.

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Newborns have an innate system for preferentially looking at an upright human face. This face preference behaviour disappears at approximately one month of age and reappears a few months later. However, the neural mechanisms underlying this U-shaped behavioural change remain unclear. Here, we isolate the functional development of the cortical visual pathway for face processing using S-cone-isolating stimulation, which blinds the subcortical visual pathway. Using luminance stimuli, which are conveyed by both the subcortical and cortical visual pathways, the preference for upright faces was not

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25

Frost, Douglas O. "Functional organization of surgically created visual circuits." Restorative Neurology and Neuroscience 15, no. 2-3 (1999): 107–13. https://doi.org/10.3233/rnn-1999-00125.

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Lesions of eerebral targets of the retina in newborn hamsters, when combined with transection of lemniscal pathways to the primary auditory or somatosensory thalamic nuclei or the secondary thalamic visual nucleus, can induce the formation of permanent retinal projections to the deafferented non-visual structures. These projections are retinotopically organized and form functional synapses. Consequently, neurons in the auditory or somatosensory cortices, which normally are not driven by visual stimuli, become visually responsive and have receptive field properties that ressemble, in several im

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26

Allen, Christopher P. G., Petroc Sumner, and Christopher D. Chambers. "The Timing and Neuroanatomy of Conscious Vision as Revealed by TMS-induced Blindsight." Journal of Cognitive Neuroscience 26, no. 7 (2014): 1507–18. http://dx.doi.org/10.1162/jocn_a_00557.

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Following damage to the primary visual cortex, some patients exhibit “blindsight,” where they report a loss of awareness while retaining the ability to discriminate visual stimuli above chance. Transient disruption of occipital regions with TMS can produce a similar dissociation, known as TMS-induced blindsight. The neural basis of this residual vision is controversial, with some studies attributing it to the retinotectal pathway via the superior colliculus whereas others implicate spared projections that originate predominantly from the LGN. Here we contrasted these accounts by combining TMS

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27

Brandes, Ulrik, Tim Dwyer, and Falk Schreiber. "Visual Understanding of Metabolic Pathways Across Organisms Using Layout in Two and a Half Dimensions." Journal of Integrative Bioinformatics 1, no. 1 (2004): 11–26. http://dx.doi.org/10.1515/jib-2004-2.

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Summary We propose a method for visualizing a set of related metabolic pathways across organisms using 2 1/2 dimensional graph visualization. Interdependent, twodimensional layouts of each pathway are stacked on top of each other so that biologists get a full picture of subtle and significant differences among the pathways. The (dis)similarities between pathways are expressed by the Hamming distances of the underlying graphs which are used to compute a stacking order for the pathways. Layouts are determined by a global layout of the union of all pathway graphs using a variant of the proven Sug

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28

IWATA, MAKOTO. "Visual Association Pathways in Human Brain." Tohoku Journal of Experimental Medicine 161, Supplement (1990): 61–78. http://dx.doi.org/10.1620/tjem.161.supplement_61.

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29

Lindblom, Bertil. "Optic chiasm and retrochiasmal visual pathways." Current Opinion in Ophthalmology 2, no. 5 (1991): 538–43. http://dx.doi.org/10.1097/00055735-199110000-00004.

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30

Wattam-Bell, John, Melissa Chiu, and Louisa Kulke. "Developmental Reorganisation of Visual Motion Pathways." i-Perception 3, no. 4 (2012): 230. http://dx.doi.org/10.1068/id230.

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31

Boets, B. "Eyeing visual pathways in dyslexia--Response." Science 345, no. 6196 (2014): 524. http://dx.doi.org/10.1126/science.345.6196.524-b.

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32

Rushton, D. "Development of Visual Pathways in Mammals." Journal of Neurology, Neurosurgery & Psychiatry 48, no. 2 (1985): 197–98. http://dx.doi.org/10.1136/jnnp.48.2.197-a.

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33

Wandell, Brian A., and Alex R. Wade. "Functional imaging of the visual pathways." Neurologic Clinics 21, no. 2 (2003): 417–43. http://dx.doi.org/10.1016/s0733-8619(03)00003-3.

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34

Jacobson, Daniel M. "Gliomas of the Anterior Visual Pathways." Neurosurgery Clinics of North America 10, no. 4 (1999): 683–98. http://dx.doi.org/10.1016/s1042-3680(18)30166-9.

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35

Beauchamp, Ross. "DEVELOPMENT OF VISUAL PATHWAYS IN MAMMALS." Optometry and Vision Science 62, no. 5 (1985): 357. http://dx.doi.org/10.1097/00006324-198505000-00010.

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36

Fortuyn, J. Droogleever. "Development of visual pathways in mammals." Clinical Neurology and Neurosurgery 87, no. 2 (1985): 154. http://dx.doi.org/10.1016/0303-8467(85)90126-x.

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37

Sadun, Alfredo A., and Richard M. Rubin. "The Anterior Visual Pathways???Part II." Journal of Neuro-Ophthalmology 16, no. 3 (1996): 212???222. http://dx.doi.org/10.1097/00041327-199609000-00012.

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38

Madill, S. A. "Disorders of the anterior visual pathways." Journal of Neurology, Neurosurgery & Psychiatry 75, suppl_4 (2004): iv12—iv19. http://dx.doi.org/10.1136/jnnp.2004.053421.

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39

Kudo, Motoi, Yasuhisa Nakamura, and Hironobu Tokuno. "Central visual pathways in the mole ()." Neuroscience Research Supplements 9 (January 1989): 183. http://dx.doi.org/10.1016/0921-8696(89)90968-7.

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40

de Lima Silveira, Luiz Carlos, Cézar Akiyoshi Saito, Harold Dias de Mello, et al. "Division of labor between M and P visual pathways: Different visual pathways minimize joint entropy differently." Psychology & Neuroscience 1, no. 1 (2008): 3–13. http://dx.doi.org/10.3922/j.psns.2008.1.002.

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41

atilgan, nilsu, and Sheng He. "Visual crowding effect in the Parvocellular and Magnocellular visual pathways." Journal of Vision 18, no. 10 (2018): 847. http://dx.doi.org/10.1167/18.10.847.

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42

Clifford-Jones, R. E., K. Cunningham, A. M. Halliday, et al. "Visual evoked potentials in meningiomas compressing the anterior visual pathways." Electroencephalography and Clinical Neurophysiology 61, no. 3 (1985): S52. http://dx.doi.org/10.1016/0013-4694(85)90227-5.

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43

Atilgan, Nilsu, Seung Min Yu, and Sheng He. "Visual crowding effect in the parvocellular and magnocellular visual pathways." Journal of Vision 20, no. 8 (2020): 6. http://dx.doi.org/10.1167/jov.20.8.6.

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44

Taylor, J. Eric T., Davood G. Gozli, David Chan, Greg Huffman, and Jay Pratt. "A touchy subject: advancing the modulated visual pathways account of altered vision near the hand." Translational Neuroscience 6, no. 1 (2015): 1–7. http://dx.doi.org/10.1515/tnsci-2015-0001.

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AbstractA growing body of evidence demonstrates that human vision operates differently in the space near and on the hands; for example, early findings in this literature reported that rapid onsets are detected faster near the hands, and that objects are searched more thoroughly. These and many other effects were attributed to enhanced attention via the recruitment of bimodal visual-tactile neurons representing the hand and near-hand space. However, recent research supports an alternative account: stimuli near the hands are preferentially processed by the action-oriented magnocellular visual pa

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45

Pietersen, A. N. J., S. K. Cheong, S. G. Solomon, C. Tailby, and P. R. Martin. "Temporal response properties of koniocellular (blue-on and blue-off) cells in marmoset lateral geniculate nucleus." Journal of Neurophysiology 112, no. 6 (2014): 1421–38. http://dx.doi.org/10.1152/jn.00077.2014.

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Visual perception requires integrating signals arriving at different times from parallel visual streams. For example, signals carried on the phasic-magnocellular (MC) pathway reach the cerebral cortex pathways some tens of milliseconds before signals traveling on the tonic-parvocellular (PC) pathway. Visual latencies of cells in the koniocellular (KC) pathway have not been specifically studied in simian primates. Here we compared MC and PC cells to “blue-on” (BON) and “blue-off” (BOF) KC cells; these cells carry visual signals originating in short-wavelength-sensitive (S) cones. We made extrac

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46

Ye, Qiaona, Kezheng Xu, Zidong Chen, et al. "Early impairment of magnocellular visual pathways mediated by isolated-check visual evoked potentials in primary open-angle glaucoma: a cross-sectional study." BMJ Open Ophthalmology 9, no. 1 (2024): e001463. http://dx.doi.org/10.1136/bmjophth-2023-001463.

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ObjectiveTo explore different performances in the magnocellular (MC) and parvocellular (PC) visual pathways in patients with primary open-angle glaucoma (POAG) and to objectively assess impairment in early stage of POAG.Methods and analysisThis is a cross-sectional study. MC and PC visual pathways were assessed using isolated-check visual evoked potential (ic-VEP). Visual acuity, intraocular pressure, fundus examination, optical coherence tomography and visual field were measured. Signal-to-noise ratios (SNRs), mediated by ic-VEP were recorded. The Spearman’s correlation analysis was used to e

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47

Findlay, John M., and Robin Walker. "A model of saccade generation based on parallel processing and competitive inhibition." Behavioral and Brain Sciences 22, no. 4 (1999): 661–74. http://dx.doi.org/10.1017/s0140525x99002150.

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During active vision, the eyes continually scan the visual environment using saccadic scanning movements. This target article presents an information processing model for the control of these movements, with some close parallels to established physiological processes in the oculomotor system. Two separate pathways are concerned with the spatial and the temporal programming of the movement. In the temporal pathway there is spatially distributed coding and the saccade target is selected from a “salience map.” Both pathways descend through a hierarchy of levels, the lower ones operating automatic

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48

Khairunnisa, Aulia. "Homonymous Hemianopia dan Stroke: Aspek Visual dari Penyakit Serebrovaskular." Majalah Kesehatan Indonesia 2, no. 2 (2021): 45–48. http://dx.doi.org/10.47679/makein.202129.

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Visual impairment due to stroke impacts quality of life and causes loss of vision pathways and depression. Vascular occlusion in afferent or efferent visual pathways can cause a myriad of effects. Homonymous hemianopia is a visual field list that, if there is a lesion in one area, can cause visual disturbances. Vascular causes are the most common cause of lesion occlusion in the retro chiasmal visual pathway. Clinical manifestations can include blindness of one eye, bitemporal hemianopia, binasal hemianopia, hemianopia homonym dextra / left. In the history, the patient often complains of crash

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49

Freud, Erez, Marlene Behrmann, and Jacqueline C. Snow. "What Does Dorsal Cortex Contribute to Perception?" Open Mind 4 (August 2020): 40–56. http://dx.doi.org/10.1162/opmi_a_00033.

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According to the influential “Two Visual Pathways” hypothesis, the cortical visual system is segregated into two pathways, with the ventral, occipitotemporal pathway subserving object perception, and the dorsal, occipitoparietal pathway subserving the visuomotor control of action. However, growing evidence suggests that the dorsal pathway also plays a functional role in object perception. In the current article, we present evidence that the dorsal pathway contributes uniquely to the perception of a range of visuospatial attributes that are not redundant with representations in ventral cortex.

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50

Roth, Eatai, Robert W. Hall, Thomas L. Daniel, and Simon Sponberg. "Integration of parallel mechanosensory and visual pathways resolved through sensory conflict." Proceedings of the National Academy of Sciences 113, no. 45 (2016): 12832–37. http://dx.doi.org/10.1073/pnas.1522419113.

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The acquisition of information from parallel sensory pathways is a hallmark of coordinated movement in animals. Insect flight, for example, relies on both mechanosensory and visual pathways. Our challenge is to disentangle the relative contribution of each modality to the control of behavior. Toward this end, we show an experimental and analytical framework leveraging sensory conflict, a means for independently exciting and modeling separate sensory pathways within a multisensory behavior. As a model, we examine the hovering flower-feeding behavior in the hawkmoth Manduca sexta. In the laborat

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