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Antibodies to dendritic neuronal surface antigens in opsoclonus myoclonus ataxia syndrome
Opsoclonus myoclonus ataxia syndrome (OMAS) is an autoimmune disorder characterized by rapid, random, conjugate eye movements (opsoclonus), myoclonus, and ataxia. Given these symptoms, autoantibodies targeting the cerebellum or brainstem could mediate the disease or be markers of autoimmunity. In a...
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Publicat a: | J Neuroimmunol |
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Autors principals: | , , , |
Format: | Artigo |
Idioma: | Inglês |
Publicat: |
2015
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Matèries: | |
Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4732568/ https://ncbi.nlm.nih.gov/pubmed/26298330 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jneuroim.2015.07.007 |
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