A case of anti-myelin oligodendrocyte glycoprotein (MOG) antibody-related disease with human leukocyte antigen (HLA) positivity indicative of neuro-Sweet disease
Author:
Affiliation:
1. Department of Neurology, National Hospital Organization Kumamoto Medical Center
2. Department of Neurology, National Hospital Organization Kumamotominami National Hospital
Publisher
Societas Neurologica Japonica
Subject
Clinical Neurology
Link
https://www.jstage.jst.go.jp/article/clinicalneurol/60/1/60_cn-001360/_pdf
Reference17 articles.
1. 1) Reindl M, Pauli F, Rostásy K, et al. The spectrum of MOG autoantibody-associated demyelinating diseases. Nat Rev Neurol 2013;9:455-461.
2. 2) Cobo-Calvo Á, Sepúlveda M, Bernard-Valnet R, et al. Antibodies to myelin oligodendrocyte glycoprotein in aquaporin 4 antibody seronegative longitudinally extensive transverse myelitis: Clinical and prognostic implications. Mult Scler 2016;22:312-319.
3. 3) Fujimori J, Takai Y, Nakashima I, et al. Bilateral frontal cortex encephalitis and paraparesis in a patient with anti-MOG antibodies. J Neurol Neurosurg Psychiatry 2017;88:534-536.
4. 4) Fukushima N, Suzuki M, Ogawa R, et al. A case of anti-MOG antibody-positive multiphasic disseminated encephalomyelitis co-occurring with unilateral cerebral cortical encephalitis. Clin Neurol 2017;57:723-728.
5. 5) Hisanaga K, Iwasaki Y, Itoyama Y, et al. Neuro-Sweet disease: Clinical manifestations and criteria for diagnosis. Neurology 2005;64:1756-1761.
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1. Anti-MOG antibodies associated demyelination following encephalomeningitis: Case report;Journal of Neuroimmunology;2021-04
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