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Clinical profile of patients with paraneoplastic neuromyelitis optica spectrum disorder and aquaporin-4 antibodies
BACKGROUND: In a minority of patients with neuromyelitis optica spectrum disorder (NMOSD) and aqua-porin-4 antibodies (AQP4-IgG), the disease has a paraneoplastic origin. It is unknown whether these patients have distinctive clinical features. OBJECTIVE: To report the clinical features of a series o...
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| Vydáno v: | Mult Scler |
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| Hlavní autoři: | , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5832634/ https://ncbi.nlm.nih.gov/pubmed/28920766 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1352458517731914 |
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