Evidence of Müller Glial Dysfunction in Patients with Aquaporin-4 Immunoglobulin G–Positive Neuromyelitis Optica Spectrum Disorder-Reference-Cited by-同舟云学术

Evidence of Müller Glial Dysfunction in Patients with Aquaporin-4 Immunoglobulin G–Positive Neuromyelitis Optica Spectrum Disorder

Published:2019-06 Issue:6 Volume:126 Page:801-810
ISSN:0161-6420
Container-title:Ophthalmology
language:en
Short-container-title:Ophthalmology

Author:

You Yuyi,Zhu Ling,Zhang Ting,Shen Ting,Fontes Ariadna,Yiannikas Con,Parratt John,Barton Joshua,Schulz Angela,Gupta Vivek,Barnett Michael H.,Fraser Clare L.^ORCID,Gillies Mark^ORCID,Graham Stuart L.,Klistorner Alexander

Funder

National Health and Medical Research Council

Ophthalmic Research Institute of Australia

National MS Society

Sydney Eye Hospital Foundation

Sydney Medical School Foundation

Publisher

Elsevier BV

Subject

Ophthalmology

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3. Differing structural and functional patterns of optic nerve damage in multiple sclerosis and neuromyelitis optica spectrum disorder;Shen;Ophthalmology,2019

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5. Radiological differentiation of optic neuritis with myelin oligodendrocyte glycoprotein antibodies, aquaporin-4 antibodies, and multiple sclerosis;Ramanathan;Mult Scler,2016

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