Neuromyelitis optica spectrum disorders with antibodies to myelin oligodendrocyte glycoprotein or aquaporin-4: Clinical and paraclinical characteristics in Algerian patients-Reference-Cited by-同舟云学术

Neuromyelitis optica spectrum disorders with antibodies to myelin oligodendrocyte glycoprotein or aquaporin-4: Clinical and paraclinical characteristics in Algerian patients

Published:2017-10 Issue: Volume:381 Page:240-244
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Bouzar Melissa,Daoudi Smail,Hattab Samira,Bouzar Amel A.,Deiva Kumaran,Wildemann Brigitte,Reindl Markus,Jarius Sven

Funder

Dietmar Hopp

Merck Serono

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference25 articles.

1. Neuromyelitis optica: clinical features, immunopathogenesis and treatment;Jarius;Clin. Exp. Immunol.,2014

2. The history of neuromyelitis optica;Jarius;J. Neuroinflammation,2013

3. International consensus diagnostic criteria for neuromyelitis optica spectrum disorders;Wingerchuk;Neurology,2015

4. Complement activating antibodies to myelin oligodendrocyte glycoprotein in neuromyelitis optica and related disorders;Mader;J. Neuroinflammation,2011

5. Myelin-oligodendrocyte glycoprotein antibodies in adults with a neuromyelitis optica phenotype;Kitley;Neurology,2012

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