Characterization of neuromyelitis optica and neuromyelitis optica spectrum disorder patients with a late onset
- Kuscu, D.
- Palace, J.
- Confavreux, C.
- Saips, S.
- Sivas, A.
- Altintas, A.
- Akman-Demirs, G.
- De Seze, J.
- Collongues, N.
- Marignier, R.
- Jacob, A.
- Leite, M. I.
- Paul, F.
- Zephir, H.
- Elsone, L.
- Jarius, S.
- Papeix, C.
- Mutch, K.
- Wildemann, B.
- Kitley, J.
- Karabudak, R.
- Aktas, O.
Publication date
January 2014
DOI Publisher
SAGE Publications Journal
Multiple Sclerosis JournalAbstract
Background: Few data are available for patients with a late onset (>= 50 years) of neuromyelitis optica (LONMO) or neuromyelitis optica spectrum disease (LONMOSD), defined by an optic neuritis/longitudinally extensive transverse myelitis with aquaporin-4 antibodies (AQP4-Ab)
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