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Effect of paraoxonase 1 gene polymorphisms on clinical course of Henoch-Schonlein purpura

dc.contributor.authorErgen, Arzu
dc.contributor.authorİsbir, TURGAY
dc.contributor.authorAgachan, Bedia
dc.contributor.authorYilmaz, Alev
dc.contributor.authorYilmaz, HÜLYA
dc.contributor.authorSirin, Aydan
dc.contributor.authorEmre, Sevinc
dc.contributor.authorBilge, Ilmay
dc.date.accessioned2021-03-03T17:56:31Z
dc.date.available2021-03-03T17:56:31Z
dc.date.issued2009
dc.identifier.citationYilmaz A., Emre S., Agachan B., Bilge I., Yilmaz H., Ergen A., İsbir T., Sirin A., "Effect of paraoxonase 1 gene polymorphisms on clinical course of Henoch-Schonlein purpura", JOURNAL OF NEPHROLOGY, cilt.22, sa.6, ss.726-732, 2009
dc.identifier.issn1121-8428
dc.identifier.othervv_1032021
dc.identifier.otherav_4c546c3a-329d-4998-8eb3-95a8de91b45e
dc.identifier.urihttp://hdl.handle.net/20.500.12627/54682
dc.description.abstractBackground: Henoch-Schonlein purpura (HSP) is a systemic vasculitis; its pathogenesis is still unknown. Oxidative stress may play a role in the pathogenesis of HSP. Paraoxonase1 (PON1) is an antioxidant enzyme. Two polymorphisms have been defined in the coding region of the PON1 gene, Q/R192 and L/M55. In the present study, we aimed to investigate the effect of PON1 gene polymorphisms on the course and renal involvement of HSP in Turkish children.
dc.language.isoeng
dc.subjectNefroloji
dc.subjectSağlık Bilimleri
dc.subjectİç Hastalıkları
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectÜROLOJİ VE NEFROLOJİ
dc.titleEffect of paraoxonase 1 gene polymorphisms on clinical course of Henoch-Schonlein purpura
dc.typeMakale
dc.relation.journalJOURNAL OF NEPHROLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume22
dc.identifier.issue6
dc.identifier.startpage726
dc.identifier.endpage732
dc.contributor.firstauthorID69224


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