MOG Antibody Disease: Nuances in Presentation, Diagnosis, and Management
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s11910-024-01344-z.pdf
Reference127 articles.
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2. Ciotti JR, Eby NS, Wu GF, Naismith RT, Chahin S, Cross AH. Clinical and laboratory features distinguishing MOG antibody disease from multiple sclerosis and AQP4 antibody-positive neuromyelitis optica. Mult Scler Relat Disord. 2020;45:102399. https://doi.org/10.1016/j.msard.2020.102399.
3. •• Banwell B, Bennett JL, Marignier R, Kim HJ, Brilot F, Flanagan EP, et al. Diagnosis of myelin oligodendrocyte glycoprotein antibody-associated disease: International MOGAD Panel proposed criteria. Lancet Neurol. 2023;22(3):268–82. https://doi.org/10.1016/S1474-4422(22)00431-8. (This proposed diagnostic criteria, as determined by an international panel of neuroimmunology experts, defines MOG antibody disease and accounts for common clinical presentations and MOG antibody titers.)
4. Johns TG, Bernard CC. The structure and function of myelin oligodendrocyte glycoprotein. J Neurochem. 1999;72(1):1–9. https://doi.org/10.1046/j.1471-4159.1999.0720001.x.
5. Peschl P, Bradl M, Höftberger R, Berger T, Reindl M. Myelin Oligodendrocyte Glycoprotein: Deciphering a Target in Inflammatory Demyelinating Diseases. Front Immunol. 2017;8(8):529. https://doi.org/10.3389/fimmu.2017.00529.
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