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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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| 出版年: | Sci China Life Sci |
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| 主要な著者: | , , , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2016
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| 主題: | |
| オンライン･アクセス: | 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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