Retinal vein occlusion in young patients: Combined MTHFR and PAI-1 mutations

Basit Öğe Kaydı
dc.authorscopusid11142262000
dc.authorscopusid8065719600
dc.authorscopusid36482717600
dc.authorscopusid56254195100
dc.contributor.authorErdurmuş, Mesut
dc.contributor.authorÇelebi, Serdal
dc.contributor.authorDüzenli Gepdiremen, Selma
dc.contributor.authorÇelebi, Harika
dc.date.accessioned2024-09-25T19:43:17Z
dc.date.available2024-09-25T19:43:17Z
dc.date.issued2012
dc.departmentAbant İzzet Baysal Üniversitesien_US
dc.description.abstractIn this case presentation, we reported 3 young patients with retinal vein occlusion. None of the patients showed any risc factors at the end of detailed systemic examinations. Methylenetetrahydrofolate reductase C677T and A1298C with plasminogen activator inhibitor-1 heterozygote gene mutations were detected in all patients on genetic analysis. The presence of thrombophilic risk factors should be considered in young patients with central retinal vein occlusion.en_US
dc.identifier.endpage58en_US
dc.identifier.issn1300-1256
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-84862077020en_US
dc.identifier.scopusqualityQ4en_US
dc.identifier.startpage54en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12491/12522
dc.identifier.volume20en_US
dc.indekslendigikaynakScopusen_US
dc.language.isotren_US
dc.relation.ispartofRetina-Vitreusen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.snmzYK_20240925en_US
dc.subjectRetinal vein occlusionen_US
dc.subjectThrombophilic risk factorsen_US
dc.subjectYoung adultsen_US
dc.titleRetinal vein occlusion in young patients: Combined MTHFR and PAI-1 mutationsen_US
dc.title.alternativeGenç olgularda retinal ven oklüzyonu: MTHFR ve PAI-1 mutasyonu birlikteli?i]en_US
dc.typeArticleen_US

Dosyalar

Koleksiyon

Scopus İndeksli Yayınlar Koleksiyonu