Autoantibody to MOG suggests two distinct clinical subtypes of NMOSD

We characterized a unique group of patients with neuromyelitis optica spectrum disorder (NMOSD) who carried autoantibodies of aquaporin-4 (AQP4) and myelin-oligodendrocyte glycoprotein (MOG). Among the 125 NMOSD patients, 10 (8.0%) were AQP4- and MOG-ab double positive, and 14 (11.2%) were MOG-ab si...

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Pubblicato in:Sci China Life Sci
Autori principali: Yan, Yaping, Li, Yujing, Fu, Ying, Yang, Li, Su, Lei, Shi, Kaibin, Li, Minshu, Liu, Qiang, Borazanci, Aimee, Liu, Yaou, He, Yong, Bennett, Jeffrey L., Vollmer, Timothy L., Shi, Fu-Dong
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2016
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5101174/
https://ncbi.nlm.nih.gov/pubmed/26920678
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11427-015-4997-y
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