Multiple thromboses at multiple sites A known hereditary disease emerging late but suddenly and extensively

Basit Öğe Kaydı
dc.authoridOzcan, Firat/0000-0002-7954-7839
dc.contributor.authorOzcan, F.
dc.contributor.authorSen, N.
dc.contributor.authorTurak, O.
dc.contributor.authorOkten, S.
dc.contributor.authorOzlu, M. F.
dc.date.accessioned2024-09-18T20:27:55Z
dc.date.available2024-09-18T20:27:55Z
dc.date.issued2012
dc.departmentHatay Mustafa Kemal Üniversitesien_US
dc.description.abstractHyperhomocysteinemia is a significant independent, usually heritable, prothrombotic risk factor for atherothrombotic cardiovascular, cerebrovascular, and peripheral vascular disease. We report a 42-year-old woman who had multiple embolic events.en_US
dc.identifier.doi10.1007/s00059-011-3565-x
dc.identifier.endpage455en_US
dc.identifier.issn0340-9937
dc.identifier.issue4en_US
dc.identifier.pmid22193948en_US
dc.identifier.scopus2-s2.0-84864253500en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage453en_US
dc.identifier.urihttps://doi.org/10.1007/s00059-011-3565-x
dc.identifier.urihttps://hdl.handle.net/20.500.12483/10597
dc.identifier.volume37en_US
dc.identifier.wosWOS:000305737700013en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherUrban & Vogelen_US
dc.relation.ispartofHerzen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectHyperhomocysteinemiaen_US
dc.subjectMethylenetetrahydrofolate reductase gene mutationen_US
dc.subjectMyocardial infarctionen_US
dc.subjectHypercoagulabilityen_US
dc.subjectThrombolytic therapyen_US
dc.titleMultiple thromboses at multiple sites A known hereditary disease emerging late but suddenly and extensivelyen_US
dc.typeArticleen_US

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