Zobrazeno 1 - 10
of 159
pro vyhledávání: '"A. Herbik"'
Autor:
Robert J. Puzniak, Brent McPherson, Khazar Ahmadi, Anne Herbik, Jörn Kaufmann, Thomas Liebe, Andre Gouws, Antony B. Morland, Irene Gottlob, Michael B. Hoffmann, Franco Pestilli
Publikováno v:
Scientific Data, Vol 8, Iss 1, Pp 1-19 (2021)
Measurement(s) brain white matter Technology Type(s) magnetic resonance imaging Sample Characteristic - Organism Homo sapiens Machine-accessible metadata file describing the reported data: https://doi.org/10.6084/m9.figshare.16726246
Externí odkaz:
https://doaj.org/article/d13e3dc669d043cba0388f41862fc551
Autor:
Herbik, Magdalena
Publikováno v:
Polityka Unii Europejskiej wobec partnerów azjatyckich / The European Union Policy towards Asian Partners. :195-223
Externí odkaz:
https://www.ceeol.com/search/chapter-detail?id=870635
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
Autor:
Ahmadi, Khazar, Herbik, Anne, Wagner, Markus, Kanowski, Martin, Thieme, Hagen, Hoffmann, Michael B.
Publikováno v:
In NeuroImage 15 November 2019 202
Publikováno v:
In Clinical Neurophysiology March 2019 130(3):379-387
Akademický článek
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Autor:
Stefan Pollmann, Lisa Rosenblum, Stefanie Linnhoff, Eleonora Porracin, Franziska Geringswald, Anne Herbik, Katja Renner, Michael B. Hoffmann
Publikováno v:
Brain Sciences, Vol 10, Iss 12, p 941 (2020)
Foveal vision loss has been shown to reduce efficient visual search guidance due to contextual cueing by incidentally learned contexts. However, previous studies used artificial (T- among L-shape) search paradigms that prevent the memorization of a t
Externí odkaz:
https://doaj.org/article/60c8706146d24f9eabe3d9dc2af97a5f
Publikováno v:
In Clinical Neurophysiology December 2014 125(12):2418-2426
Publikováno v:
In Clinical Neurophysiology June 2013 124(6):1225-1231