Acute and Chronic Management of Neuromyelitis Optica Spectrum Disorder

Author:

Sherman Elena,Han May H.

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical)

Reference46 articles.

1. Pittock SJ, Weinshenker BG, Lucchinetti CF, Wingerchuk DM, Corboy JR, Lennon VA. Neuromyelitis optica brain lesions localized at sites of high aquaporin 4 expression. Arch Neurol. 2006;63(7):964–8. doi: 10.1001/archneur.63.7.964 .

2. Pittock SJ, Lucchinetti CF. Neuromyelitis optica and the evolving spectrum of autoimmune aquaporin-4 channelopathies: a decade later. Ann N Y Acad Sci. 2015. doi: 10.1111/nyas.12794 . Provides a comprehensive review of NMOSD including clinical features, pathophysiology, diagnostic testing, and current and emerging therapeutic options.

3. Bizzoco E, Lolli F, Repice AM, Hakiki B, Falcini M, Barilaro A, et al. Prevalence of neuromyelitis optica spectrum disorder and phenotype distribution. J Neurol. 2009;256(11):1891–8. doi: 10.1007/s00415-009-5171-x .

4. Wingerchuk DM, Banwell B, Bennett JL, Cabre P, Carroll W, Chitnis T, et al. International consensus diagnostic criteria for neuromyelitis optica spectrum disorders. Neurology. 2015;85(2):177–89. doi: 10.1212/wnl.0000000000001729 . Most recent publication of consensus criteria for NMOSD including criteria for diagnosis in patients who are both antibody positive and negative. Provides excellent description of less-common presentations of NMO and radiologic findings that can be suggestive of diesease.

5. Wingerchuk DM, Lennon VA, Pittock SJ, Lucchinetti CF, Weinshenker BG. Revised diagnostic criteria for neuromyelitis optica. Neurology. 2006;66(10):1485–9. doi: 10.1212/01.wnl.0000216139.44259.74 .

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