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Isolated dysphagia due to aquaporin-4 autoimmunity

dc.contributor.authorTürkoğlu, Recai
dc.contributor.authorKıyat-Atamer, Aslı
dc.contributor.authorTüzün, Erdem
dc.contributor.authorAkman-Demir, Gülşen
dc.date.accessioned2016-12-22T10:27:41Z
dc.date.available2016-12-22T10:27:41Z
dc.date.issued2012
dc.identifier.citationTurkoglu R, Kiyat-Atamer A, Tuzun E, Akman-Demir G. Isolated dysphagia due to aquaporin-4 autoimmunity. Turk J Gastroenterol 2012; 23 (6): 804-805. doi: 10.4318/tjg.2012.0437en_US
dc.identifier.issn1300-4948
dc.identifier.urihttps://hdl.handle.net/11446/1223en_US
dc.identifier.urihttp://www.turkjgastroenterol.org/sayilar/208/buyuk/13181.pdfen_US
dc.descriptionİstanbul Bilim Üniversitesi, Tıp Fakültesi.en_US
dc.description.abstractNeuromyelitis optica (NMO) is an inflammatory, demyelinating disease that affects the spinal cord and optic nerves and is associated with aquaporin- 4 antibodies (Aqp-4 Ab). NMO patients might occasionally present with medulla symptoms such as hiccups, nausea and vomiting and with small lesions in the dorsal medulla, which corresponds to a site of high Aqp-4 expression.en_US
dc.language.isoengen_US
dc.publisherAves Yayıncılıken_US
dc.identifier.doi10.4318/tjg.2012.0437en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectneuromyelitis opticaen_US
dc.titleIsolated dysphagia due to aquaporin-4 autoimmunityen_US
dc.title.alternativeAquaporin-4 otoimmünitesine bağlı izole disfajien_US
dc.typeletteren_US
dc.relation.journalTurkish Journal of Gastroenterologyen_US
dc.departmentDBÜ, Tıp Fakültesien_US
dc.identifier.issue6
dc.identifier.volume23
dc.identifier.startpage804
dc.identifier.endpage805
dc.contributor.authorIDTR194327en_US
dc.contributor.authorIDTR156716en_US
dc.contributor.authorIDTR24384en_US
dc.relation.publicationcategoryDiğeren_US


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