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- W2407005293 abstract "Diagnostic criteria for neuromyelitis optica (NMO) require the presence of optic neuritis and myelitis plus at least two of the following features: (1) brain MRI not consistent with multiple sclerosis (MS); (2) “longitudinally extensive” transverse myelitis (LETM: MRI-detected cord lesion spanning ≥3 vertebral segments); and (3) seropositivity for NMO-IgG, an autoantibody that targets aquaporin-4 ( Neurology 2006; 66:1485). NMO-IgG is approximately 75% sensitive for NMO ( Lancet 2004; 364:2106). In Japan, Asian “opticospinal” MS (OSMS) is recognized as a distinct phenotype that comprises 30% of CNS demyelinating disease. OSMS and NMO may be the same disorder.To assess the diagnostic utility of an assay that uses …" @default.
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- W2407005293 date "2007-01-01" @default.
- W2407005293 modified "2023-09-28" @default.
- W2407005293 title "Aquaporin-4 Antibodies, Neuromyelitis Optica, and Multiple Sclerosis" @default.
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- W2407005293 doi "https://doi.org/10.1056/jn200707310000002" @default.
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