Characterization of neuromyelitis optica and neuromyelitis optica spectrum disorder patients with a late onset

Tarih
2014
Yazar
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.
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Özet
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).
Bağlantı
http://hdl.handle.net/20.500.12627/126918
https://doi.org/10.1177/1352458513515085
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