AQP4-IgG-seropositive neuromyelitis optica spectrum disorder (NMOSD) coexisting with anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis: A case report and literature review
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology,General Medicine
Reference15 articles.
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2. The intrinsic pathogenic role of autoantibodies to aquaporin 4 mediating spinal cord disease in a rat passive-transfer model;Christian;Exp. Neurol.,2015
3. Comparison of myelin oligodendrocyte glycoprotein (MOG)-antibody disease and AQP4-IgG-positive neuromyelitis optica spectrum disorder (NMOSD) when they co-exist with anti-NMDA (N-methyl-D-aspartate) receptor encephalitis;Fan;Mult. Scler. Relat. Disord.,2018
4. A clinical approach to diagnosis of autoimmune encephalitis;Graus;Lancet Neurol.,2016
5. Cellular and synaptic mechanisms of anti-NMDA receptor encephalitis;Hughes;J. Neurosci.,2010
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2. Factors associated with disease relapse rate in the Neuromyelitis optica spectrum disorder;International Journal of Neuroscience;2023-07-26
3. Pediatric Neuromyelitis Optica Spectrum Disorder;Seminars in Pediatric Neurology;2023-07
4. Autoimmune encephalitis with anti-NMDAR antibodies – variety of clinical manifestations;Aktualności Neurologiczne;2023
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