Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Pieter B de Best"'
Structural changes to primary visual cortex in the congenital absence of cone input in achromatopsia
Autor:
Barbara Molz, Anne Herbik, Heidi A. Baseler, Pieter B. de Best, Richard W. Vernon, Noa Raz, Andre D. Gouws, Khazar Ahmadi, Rebecca Lowndes, Rebecca J. McLean, Irene Gottlob, Susanne Kohl, Lars Choritz, John Maguire, Martin Kanowski, Barbara Käsmann-Kellner, Ilse Wieland, Eyal Banin, Netta Levin, Michael B. Hoffmann, Antony B. Morland
Publikováno v:
NeuroImage: Clinical, Vol 33, Iss , Pp 102925- (2022)
Autosomal recessive Achromatopsia (ACHM) is a rare inherited disorder associated with dysfunctional cone photoreceptors resulting in a congenital absence of cone input to visual cortex. This might lead to distinct changes in cortical architecture wit
Externí odkaz:
https://doaj.org/article/5b376ad1773c4fc9a913d40790812f34
Autor:
Rebecca Lowndes, Barbara Molz, Lucy Warriner, Anne Herbik, Pieter B. de Best, Noa Raz, Andre Gouws, Khazar Ahmadi, Rebecca J. McLean, Irene Gottlob, Susanne Kohl, Lars Choritz, John Maguire, Martin Kanowski, Barbara Käsmann-Kellner, Ilse Wieland, Eyal Banin, Netta Levin, Michael B. Hoffmann, Antony B. Morland, Heidi A. Baseler
Publikováno v:
Frontiers in Neuroscience, Vol 15 (2021)
Most individuals with congenital achromatopsia (ACHM) carry mutations that affect the retinal phototransduction pathway of cone photoreceptors, fundamental to both high acuity vision and colour perception. As the central fovea is occupied solely by c
Externí odkaz:
https://doaj.org/article/f802a11afd7945488b5067da8e56a31e
Structural changes to primary visual cortex in the congenital absence of cone input in achromatopsia
Autor:
Andre Gouws, Anne Herbik, Susanne Kohl, Netta Levin, Khazar Ahmadi, Eyal Banin, Barbara Molz, John Maguire, Lars Choritz, Rebecca Lowndes, Antony B. Morland, Noa Raz, Barbara Käsmann-Kellner, Heidi A. Baseler, Irene Gottlob, Richard J. W. Vernon, Rebecca J. McLean, Ilse Wieland, Michael B. Hoffmann, Martin Kanowski, Pieter B. de Best
Autosomal recessive Achromatopsia (ACHM) is a rare inherited disorder associated with dysfunctional cone photoreceptors resulting in a congenital absence of cone input to visual cortex. This might lead to distinct changes in cortical architecture wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8854c9a1248a2dc8a6d5346913b77a6
https://doi.org/10.1101/2021.07.19.21260427
https://doi.org/10.1101/2021.07.19.21260427
Autor:
Yoni Pertzov, Netta Levin, Serge O. Dumoulin, Noa Raz, Pieter B de Best, Nitzan Guy, Tamir Ben-Hur
Publikováno v:
JAMA Neurology, 76(11), 1391-1396. American Medical Association
De Best, P B, Raz, N, Guy, N, Ben-Hur, T, Dumoulin, S O, Pertzov, Y & Levin, N 2019, ' Role of Population Receptive Field Size in Complex Visual Dysfunctions : A Posterior Cortical Atrophy Model ', JAMA Neurology, vol. 76, no. 11, pp. 1391-1396 . https://doi.org/10.1001/jamaneurol.2019.2447
JAMA Neurology, 76, 1391-1396. American Medical Association
JAMA Neurol
De Best, P B, Raz, N, Guy, N, Ben-Hur, T, Dumoulin, S O, Pertzov, Y & Levin, N 2019, ' Role of Population Receptive Field Size in Complex Visual Dysfunctions : A Posterior Cortical Atrophy Model ', JAMA Neurology, vol. 76, no. 11, pp. 1391-1396 . https://doi.org/10.1001/jamaneurol.2019.2447
JAMA Neurology, 76, 1391-1396. American Medical Association
JAMA Neurol
Importance: The neuronal mechanism of visual agnosia and foveal crowding that underlies the behavioral symptoms of several classic neurodegenerative diseases, including impaired holistic perception, navigation, and reading, is still unclear. A better
Publikováno v:
Investigative Ophthalmology & Visual Science
Investigative Opthalmology & Visual Science
Investigative Opthalmology & Visual Science
Purpose Posterior cortical atrophy (PCA) is a rare neurodegenerative syndrome manifesting with visuospatial processing impairment. We recently suggested that abnormal population receptive field properties are associated with the symptoms of PCA patie
Autor:
Anne Herbik, Irene Gottlob, Rebecca J. McLean, Eyal Banin, Michael B. Hoffmann, Lars Choritz, Pieter B. de Best, Netta Levin, Ilse Wieland, Susanne Kohl, Richard J. W. Vernon, Noa Raz, Andre Gouws, Barbara Molz, Barbara Käsmann-Kellner, Khazar Ahmadi, Martin Kanowski, John Maguire, Antony B. Morland, Heidi A. Baseler, Rebecca Lowndes
Publikováno v:
Journal of Vision. 21:2362
Autor:
Pieter B. de Best, Noa Raz, Nitzan Guy, Tamir Ben-Hur, Serge O. Dumoulin, Yoni Pertzov, Netta Levin
Publikováno v:
JAMA Neurology
Autor:
Lowndes, Rebecca, Molz, Barbara, Warriner, Lucy, Herbik, Anne, de Best, Pieter B., Raz, Noa, Gouws, Andre, Ahmadi, Khazar, McLean, Rebecca J., Gottlob, Irene, Kohl, Susanne, Choritz, Lars, Maguire, John, Kanowski, Martin, Käsmann-Kellner, Barbara, Wieland, Ilse, Banin, Eyal, Levin, Netta, Hoffmann, Michael B., Morland, Antony B.
Publikováno v:
Frontiers in Neuroscience; 10/14/2021, Vol. 15, p1-10, 10p
Autor:
de Best, Pieter B., Raz, Noa, Guy, Nitzan, Ben-Hur, Tamir, Dumoulin, Serge O., Pertzov, Yoni, Levin, Netta
Publikováno v:
JAMA Neurology; Nov2019, Vol. 76 Issue 11, p1391-1396, 6p