A protean disease: The phenotypic range of neuromyelitis optica spectrum disorder

Abstract

Keywords

Neuromyelitis optica spectrum disorder late onset

Get full access to this article

View all access options for this article.

References

Sechi

Addis

Batzu

et al . Late presentation of NMOSD as rapidly progressive leukoencephalopathy with atypical clinical and radiological findings. Mult Scler 2018; 24: 685–688.

Wingerchuk

Banwell

Bennett

et al . International consensus diagnostic criteria for neuromyelitis optica spectrum disorders. Neurology 2015; 85: 177–189.

Magana

Matiello

Pittock

et al . Posterior reversible encephalopathy syndrome in neuromyelitis optica spectrum disorders. Neurology 2009; 72: 712–717.

Seok

Cho

Ahn

et al . Clinical characteristics of late-onset neuromyelitis optica spectrum disorder: A multicenter retrospective study in Korea. Mult Scler 2017; 23: 1748–1756.

Kim

Waters

Woodhall

et al . Gender effect on neuromyelitis optica spectrum disorder with aquaporin4-immunoglobulin G. Mult Scler 2017; 23: 1104–1111.

Mao

Yin

Zhong

et al . Late-onset neuromyelitis optica spectrum disorder in AQP4-seropositivepatients in a Chinese population. BMC Neurol 2015; 15: 160.

Collongues

Marignier

Jacob

et al . Characterization of neuromyelitis optica and neuromyelitis optica spectrum disorder patients with a late onset. Mult Scler 2014; 20: 1086–1094.

Cai

Chu

et al . Paraneoplastic neuromyelitis optica spectrum disorders: Three new cases and a review of the literature. The Int J Neurosci 2016; 126: 660–668.