Clinical features and prognosis of late-onset neuromyelitis optica spectrum disorders in a Latin American cohort-Reference-Cited by-同舟云学术

Clinical features and prognosis of late-onset neuromyelitis optica spectrum disorders in a Latin American cohort

Published:2020-01-13 Issue:5 Volume:267 Page:1260-1268
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Carnero Contentti Edgar^ORCID,Daccach Marques Vanessa,Soto de Castillo Ibis,Tkachuk Verónica,Ariel Bustos,Castillo Maria C.,Cristiano Edgardo,Diégues Serva Gabriel Braga,dos Santos Antonio Carlos,Finkelsteyn Ana Mariel,López Pablo A.,Patrucco Liliana,Molina Omaira,Pettinicchi Juan Pablo,Toneguzzo Vanesa,Caride Alejandro,Rojas Juan Ignacio

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-020-09699-2.pdf

Reference27 articles.

1. Wingerchuk DM, Lennon VA, Lucchinetti CF et al (2007) The spectrum of neuromyelitis optica. Lancet Neurol 6:805–815

2. Carnero Contentti E, De Virgiliis M, Hryb JP et al (2019) Aquaporin-4 serostatus and visual outcomes in clinically isolated acute optic neuritis. J Neuroophthalmol 39(2):165–169

3. Akman-Demir G, Tüzün E, Waters P et al (2011) Prognostic implications of aquaporin-4 antibody status in neuromyelitis optica patients. J Neurol 258(3):464–470

4. Wingerchuk D, Banwell B, Bennett J et al (2015) International consensus diagnostic criteria for neuromyelitis optica spectrum disorders. Neurology 85:177–189

5. Lennon V, Wingerchuk D, Kryzer T et al (2004) A serum autoantibody marker of neuromyelitis optica: distinction from multiple sclerosis. Lancet 364:2106–2112

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