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dc.contributor.authorKuscu, D.
dc.contributor.authorPalace, J.
dc.contributor.authorConfavreux, C.
dc.contributor.authorSaips, S.
dc.contributor.authorSivas, A.
dc.contributor.authorAltintas, A.
dc.contributor.authorAkman-Demirs, G.
dc.contributor.authorDe Seze, J.
dc.contributor.authorCollongues, N.
dc.contributor.authorMarignier, R.
dc.contributor.authorJacob, A.
dc.contributor.authorLeite, M. I.
dc.contributor.authorPaul, F.
dc.contributor.authorZephir, H.
dc.contributor.authorElsone, L.
dc.contributor.authorJarius, S.
dc.contributor.authorPapeix, C.
dc.contributor.authorMutch, K.
dc.contributor.authorWildemann, B.
dc.contributor.authorKitley, J.
dc.contributor.authorKarabudak, R.
dc.contributor.authorAktas, O.
dc.date.accessioned2021-03-05T16:07:23Z
dc.date.available2021-03-05T16:07:23Z
dc.date.issued2014
dc.identifier.citationCollongues N., Marignier R., Jacob A., Leite M. I. , Sivas A., Paul F., Zephir H., Akman-Demirs G., Elsone L., Jarius S., et al., "Characterization of neuromyelitis optica and neuromyelitis optica spectrum disorder patients with a late onset", MULTIPLE SCLEROSIS JOURNAL, cilt.20, ss.1086-1094, 2014
dc.identifier.issn1352-4585
dc.identifier.othervv_1032021
dc.identifier.otherav_bf249dd2-732e-48d3-b360-a273821c70df
dc.identifier.urihttp://hdl.handle.net/20.500.12627/126918
dc.identifier.urihttps://doi.org/10.1177/1352458513515085
dc.description.abstractBackground: 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).
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri
dc.subjectNöroloji
dc.subjectNEUROSCIENCES
dc.subjectKLİNİK NEUROLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectDahili Tıp Bilimleri
dc.subjectSinirbilim ve Davranış
dc.titleCharacterization of neuromyelitis optica and neuromyelitis optica spectrum disorder patients with a late onset
dc.typeMakale
dc.relation.journalMULTIPLE SCLEROSIS JOURNAL
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume20
dc.identifier.issue8
dc.identifier.startpage1086
dc.identifier.endpage1094
dc.contributor.firstauthorID215575


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