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dc.contributor.authorMelms, A.
dc.contributor.authorAkman-Demir, G.
dc.contributor.authorWandinger, K. P.
dc.contributor.authorKristoferitsch, W.
dc.contributor.authorWildemann, B.
dc.contributor.authorJarius, S.
dc.contributor.authorPaul, F.
dc.contributor.authorFranciotta, D.
dc.contributor.authorde Seze, J.
dc.contributor.authorMuench, C.
dc.contributor.authorSalvetti, M.
dc.contributor.authorRuprecht, K.
dc.contributor.authorLiebetrau, M.
dc.date.accessioned2021-03-04T14:10:53Z
dc.date.available2021-03-04T14:10:53Z
dc.date.issued2012
dc.identifier.citationJarius S., Paul F., Franciotta D., de Seze J., Muench C., Salvetti M., Ruprecht K., Liebetrau M., Wandinger K. P. , Akman-Demir G., et al., "Neuromyelitis optica spectrum disorders in patients with myasthenia gravis: ten new aquaporin-4 antibody positive cases and a review of the literature", MULTIPLE SCLEROSIS JOURNAL, cilt.18, sa.8, ss.1135-1143, 2012
dc.identifier.issn1352-4585
dc.identifier.othervv_1032021
dc.identifier.otherav_802f2e84-7ee9-4a38-b83c-18f0a3da596b
dc.identifier.urihttp://hdl.handle.net/20.500.12627/87456
dc.identifier.urihttps://doi.org/10.1177/1352458511431728
dc.description.abstractBackground: Neuromyelitis optica (NMO, Devic syndrome) and myasthenia gravis (MG) are rare antibody-mediated autoimmune disorders. Concurrent incidence has been reported in only few patients, mostly non-Caucasians.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectSinirbilim ve Davranış
dc.subjectNEUROSCIENCES
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleNeuromyelitis optica spectrum disorders in patients with myasthenia gravis: ten new aquaporin-4 antibody positive cases and a review of the literature
dc.typeMakale
dc.relation.journalMULTIPLE SCLEROSIS JOURNAL
dc.contributor.departmentRuprecht Karls University Heidelberg , ,
dc.identifier.volume18
dc.identifier.issue8
dc.identifier.startpage1135
dc.identifier.endpage1143
dc.contributor.firstauthorID205281


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