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Polymorphisms in the endothelial nitric oxide synthase gene are associated with Behcet's disease

dc.contributor.authorSILMAN, A
dc.contributor.authorGul, Ahmet
dc.contributor.authorHAJEER, AH
dc.contributor.authorWORTHINGTON, J
dc.contributor.authorOLLIER, WER
dc.contributor.authorKARASNEH, JA
dc.date.accessioned2021-03-03T08:47:08Z
dc.date.available2021-03-03T08:47:08Z
dc.date.issued2005
dc.identifier.citationKARASNEH J., HAJEER A., SILMAN A., WORTHINGTON J., OLLIER W., Gul A., "Polymorphisms in the endothelial nitric oxide synthase gene are associated with Behcet's disease", RHEUMATOLOGY, cilt.44, sa.5, ss.614-617, 2005
dc.identifier.issn1462-0324
dc.identifier.otherav_19780d04-5c52-47cf-bacf-e6b980544009
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/22403
dc.identifier.urihttps://doi.org/10.1093/rheumatology/keh561
dc.description.abstractObjective. Reduced plasma nitric oxide (NO) levels in Behcet's disease (BD) patients have been implicated in the development of the endothelial abnormalities and thrombotic complications occurring in these patients. This study investigated the association of the endothelial NO Synthase (eNOS) gene polymorphisms with BD.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectİmmünoloji ve Romatoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectROMATOLOJİ
dc.titlePolymorphisms in the endothelial nitric oxide synthase gene are associated with Behcet's disease
dc.typeMakale
dc.relation.journalRHEUMATOLOGY
dc.contributor.department, ,
dc.identifier.volume44
dc.identifier.issue5
dc.identifier.startpage614
dc.identifier.endpage617
dc.contributor.firstauthorID50936


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