MOG-IgG in NMO and related disorders: a multicenter study of 50 patients. Part 4: Afferent visual system damage after optic neuritis in MOG-IgG-seropositive versus AQP4-IgG-seropositive patients

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作者
Florence Pache
Hanna Zimmermann
Janine Mikolajczak
Sophie Schumacher
Anna Lacheta
Frederike C. Oertel
Judith Bellmann-Strobl
Sven Jarius
Brigitte Wildemann
Markus Reindl
Amy Waldman
Kerstin Soelberg
Nasrin Asgari
Marius Ringelstein
Orhan Aktas
Nikolai Gross
Mathias Buttmann
Thomas Ach
Klemens Ruprecht
Friedemann Paul
Alexander U. Brandt
机构
[1] Charité – Universitätsmedizin Berlin,NeuroCure Clinical Research Center (NCRC)
[2] Charité – Universitätsmedizin Berlin,Department of Neurology
[3] University of Heidelberg,Molecular Neuroimmunology Group, Department of Neurology
[4] Medical University of Innsbruck,Clinical Department of Neurology
[5] Children’s Hospital of Philadelphia,Division of Neurology
[6] Vejle Hospital,Department of Neurology
[7] University of Southern Denmark,Department of Neurobiology, Institute of Molecular Medicine
[8] Heinrich Heine University,Department of Neurology, Medical Faculty
[9] University of Freiburg,Department of Ophthalmology, Medical Faculty
[10] University of Würzburg,Department of Neurology
[11] University of Würzburg,Department of Ophthalmology
[12] Max Delbrück Center for Molecular Medicine and Charité – Universitätsmedizin Berlin,Experimental and Clinical Research Center
关键词
Myelin oligodendrocyte glycoprotein antibodies (MOG-IgG); aquaporin-4 antibodies (AQP4-IgG); NMO-IgG; neuromyelitis optica; Devic syndrome; neuromyelitis optica spectrum disorders (NMOSD); optic neuritis; optical coherence tomography; visual evoked potentials; visual acuity; retinal neuro-axonal damage;
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