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dc.contributor.authorGurdol, Figen Melek
dc.contributor.authorİsbir, TURGAY
dc.contributor.authorUnlucerci, Yaşar Meryem Yeşim
dc.contributor.authorYılmaz, H
dc.contributor.authorİşbilen, Elif
dc.date.accessioned2021-03-05T17:43:20Z
dc.date.available2021-03-05T17:43:20Z
dc.date.issued2004
dc.identifier.citationYılmaz H., Unlucerci Y. M. Y. , Gurdol F. M. , İşbilen E., İsbir T., "Association of pre-eclampsia with hyperhomocysteinaemia and methylenetetrahydrofolate reductase gene C677T polymorphism in a Turkish population", AUSTRALIAN & NEW ZEALAND JOURNAL OF OBSTETRICS & GYNAECOLOGY, cilt.44, ss.423-427, 2004
dc.identifier.issn0004-8666
dc.identifier.otherav_c6e6ef3e-6a56-41cc-ba47-300f8d0fc079
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/131842
dc.identifier.urihttps://doi.org/10.1111/j.1479-828x.2004.00283.x
dc.description.abstractBackground: Hyperhomocysteinaemia is a common finding in a wide variety of pathological conditions that exhibit endothelial disturbances. In the pathogenesis of pre-eclampsia, endothelial cell activation or dysfunction has been proposed as a central feature, and the presence of hyperhomocysteinaemia in varying degrees has been detected. One of the known causes of hyperhomocysteinaemia is polymorphism in the methylenetetrahydrofolate reductase gene that lowers the activity of the enzyme.
dc.language.isoeng
dc.subjectKadın Hastalıkları ve Doğum
dc.subjectCerrahi Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKADIN HASTALIKLARI & DOĞUM
dc.titleAssociation of pre-eclampsia with hyperhomocysteinaemia and methylenetetrahydrofolate reductase gene C677T polymorphism in a Turkish population
dc.typeMakale
dc.relation.journalAUSTRALIAN & NEW ZEALAND JOURNAL OF OBSTETRICS & GYNAECOLOGY
dc.contributor.department, ,
dc.identifier.volume44
dc.identifier.issue5
dc.identifier.startpage423
dc.identifier.endpage427
dc.contributor.firstauthorID40434


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