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Structural changes to primary visual cortex in the congenital absence of cone input in achromatopsia.
Molz, Barbara; Herbik, Anne; Baseler, Heidi A; de Best, Pieter B; Vernon, Richard W; Raz, Noa; Gouws, Andre D; Ahmadi, Khazar; Lowndes, Rebecca; 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.
Afiliação
  • Molz B; Department of Psychology, University of York, Heslington, YO10 5DD York, United Kingdom; Language and Genetics Department, Max Planck Institute for Psycholinguistics, 6525 XD Nijmegen, Netherlands.
  • Herbik A; Department of Ophthalmology, University Hospital, Otto-von-Guericke University, 39120 Magdeburg, Germany.
  • Baseler HA; Department of Psychology, University of York, Heslington, YO10 5DD York, United Kingdom; Hull York Medical School, University of York, Heslington, YO10 5DD York, United Kingdom; York Biomedical Research Institute, University of York, Heslington, YO10 5DD York, United Kingdom.
  • de Best PB; MRI Unit, Department of Neurology, Hadassah Medical Center, 91120 Jerusalem, Israel.
  • Vernon RW; Department of Psychology, University of York, Heslington, YO10 5DD York, United Kingdom.
  • Raz N; MRI Unit, Department of Neurology, Hadassah Medical Center, 91120 Jerusalem, Israel.
  • Gouws AD; York Neuroimaging Centre, Department of Psychology, University of York, YO10 5NY York, United Kingdom.
  • Ahmadi K; Department of Ophthalmology, University Hospital, Otto-von-Guericke University, 39120 Magdeburg, Germany.
  • Lowndes R; York Neuroimaging Centre, Department of Psychology, University of York, YO10 5NY York, United Kingdom.
  • McLean RJ; University of Leicester Ulverscroft Eye Unit, University of Leicester, Leicester Royal Infirmary, LE2 7LX Leicester, United Kingdom.
  • Gottlob I; University of Leicester Ulverscroft Eye Unit, University of Leicester, Leicester Royal Infirmary, LE2 7LX Leicester, United Kingdom.
  • Kohl S; Molecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology, University Clinics Tübingen, 72076 Tübingen, Germany.
  • Choritz L; Department of Ophthalmology, University Hospital, Otto-von-Guericke University, 39120 Magdeburg, Germany.
  • Maguire J; School of Optometry and Vision Sciences, University of Bradford, BD7 1DP Bradford, United Kingdom.
  • Kanowski M; Department of Neurology, University Hospital, Otto-von-Guericke University, 39120 Magdeburg, Germany.
  • Käsmann-Kellner B; Department of Ophthalmology, Saarland University Hospital and Medical Faculty of the Saarland University, 66421 Homburg, Germany.
  • Wieland I; Department for Molecular Genetics, Institute for Human Genetics, University Hospital, Otto-von-Guericke University, 39120 Magdeburg, Germany.
  • Banin E; Degenerative Diseases of the Retina Unit, Department of Ophthalmology, Hadassah Medical Center, 91120 Jerusalem, Israel.
  • Levin N; MRI Unit, Department of Neurology, Hadassah Medical Center, 91120 Jerusalem, Israel.
  • Hoffmann MB; Department of Ophthalmology, University Hospital, Otto-von-Guericke University, 39120 Magdeburg, Germany; Center for Behavioral Brain Sciences, 39106 Magdeburg, Germany.
  • Morland AB; Department of Psychology, University of York, Heslington, YO10 5DD York, United Kingdom; York Biomedical Research Institute, University of York, Heslington, YO10 5DD York, United Kingdom; York Neuroimaging Centre, Department of Psychology, University of York, YO10 5NY York, United Kingdom. Electroni
Neuroimage Clin ; 33: 102925, 2022.
Article em En | MEDLINE | ID: mdl-34959047

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Córtex Visual / Defeitos da Visão Cromática Tipo de estudo: Clinical_trials Limite: Adult / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Córtex Visual / Defeitos da Visão Cromática Tipo de estudo: Clinical_trials Limite: Adult / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article