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Clinical Course, Imaging Characteristics, and Therapeutic Response in Myelin Oligodendrocyte Glycoprotein Antibody Disease: A Case Series.

PMID: 32140030 (view PubMed database entry)
DOI: 10.1055/s-0040-1701371 (read at publisher's website )
PMCID: PMC7055612 (free full text version available)

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Joe James, James Jose, V Abdul Gafoor, B Smita, Neetha Balaram, Aparna Ramachandran,

Myelin oligodendrocyte glycoprotein (MOG) antibody disease is a novel central nervous system autoimmune disorder which forms part of aquaporin 4 (AQP-4) negative, neuromyelitis optica (NMO) spectrum disorder. It has a distinct clinical profile, neuroimaging features and courses from AQP-4 positive NMO and multiple sclerosis. This article is a case series of six patients with MOG antibody disease with longitudinal follow-up for up to 8 months.

J Neurosci Rural Pract (Journal of neurosciences in rural practice)
[2020, 11(1):205-210]

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