Acute myocardial infarction, ischemic cerebrovascular disease and variceal bleeding due to portal vein thrombosis in a patient with hereditary thrombophilia
dc.contributor.buuauthor | Baran, Bülent | |
dc.contributor.buuauthor | Yılmaz, Yusuf | |
dc.contributor.buuauthor | Algın, Oktay | |
dc.contributor.buuauthor | Keskin, Murat | |
dc.contributor.buuauthor | Kıyıcı, Murat | |
dc.contributor.buuauthor | Kocamaz, Güzin | |
dc.contributor.buuauthor | Dolar, Enver | |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/İç Hastalıkları Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Radyoloji Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Gastroenteroloji Anabilim Dalı. | tr_TR |
dc.contributor.orcid | 0000-0003-4518-5283 | tr_TR |
dc.contributor.orcid | 0000-0001-7966-2346 | tr_TR |
dc.contributor.orcid | 0000-0002-3208-6211 | tr_TR |
dc.contributor.orcid | 0000-0002-3877-8366 | tr_TR |
dc.contributor.orcid | 0000-0003-4526-4352 | tr_TR |
dc.contributor.researcherid | K-6651-2012 | tr_TR |
dc.contributor.researcherid | AAG-9177-2021 | tr_TR |
dc.contributor.researcherid | A-7978-2012 | tr_TR |
dc.contributor.scopusid | 35955740500 | tr_TR |
dc.contributor.scopusid | 22936014300 | tr_TR |
dc.contributor.scopusid | 23995109100 | tr_TR |
dc.contributor.scopusid | 23050640000 | tr_TR |
dc.contributor.scopusid | 6507627491 | tr_TR |
dc.contributor.scopusid | 23995302100 | tr_TR |
dc.contributor.scopusid | 6602075084 | tr_TR |
dc.date.accessioned | 2024-02-27T07:38:18Z | |
dc.date.available | 2024-02-27T07:38:18Z | |
dc.date.issued | 2008-04 | |
dc.description.abstract | We report On a 43-year-old female patient with multiple thrombotic risk factors who, in a few months, developed acute myocardial infarction, an ischemic cerebrovascular event and variceal bleeding due to portal vein thrombosis. The factor V Leiden mutation was carried in heterozygous form, homocysteine was elevated at 19.6 mu mol/l, and methylene-tetrahydrofolate reductase C677T mutation was carried in. homozygous form. Moderately increased plasma homocysteine level and a reduced protein S activity were evident. Anticardiolipin IgG antibodies were mildly positive. We conclude that the presence of multiple genetic and environmental risk factors greatly amplifies the risk of clinical thrombotic events. | en_US |
dc.identifier.citation | Baran, B. vd. (2008). "Acute myocardial infarction, ischemic cerebrovascular disease and variceal bleeding due to portal vein thrombosis in a patient with hereditary thromblophilia". Blood Coagulation and Fibrinolysis, 19(3), 243-246. | en_US |
dc.identifier.endpage | 246 | tr_TR |
dc.identifier.issn | 0957-5235 | |
dc.identifier.issn | 1473-5733 | |
dc.identifier.issue | 3 | tr_TR |
dc.identifier.pubmed | 18388507 | |
dc.identifier.scopus | 2-s2.0-41849132863 | tr_TR |
dc.identifier.startpage | 243 | tr_TR |
dc.identifier.uri | https://doi.org/10.1097/MBC.0b013e3282f30ae5 | en_US |
dc.identifier.uri | https://journals.lww.com/bloodcoagulation/Fulltext/2008/04000/Acute_myocardial_infarction,_ischemic.12.aspx | en_US |
dc.identifier.uri | https://hdl.handle.net/11452/39989 | en_US |
dc.identifier.volume | 19 | tr_TR |
dc.identifier.wos | 000255228300012 | tr_TR |
dc.indexed.pubmed | PubMed | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.wos | SCIE | en_US |
dc.language.iso | en | en_US |
dc.publisher | Lippincott Williams & Wilkins | en_US |
dc.relation.journal | Blood Coagulation and Fibrinolysis | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Factor V Leiden mutation | en_US |
dc.subject | Hereditary thrombophilia | en_US |
dc.subject | Methylenetetrahydrofolate mutation | en_US |
dc.subject | Portal vein thrombosis | en_US |
dc.subject | Factor-v-leiden | en_US |
dc.subject | Venous thrombosi | en_US |
dc.subject | Antiphospholipid antibodies | en_US |
dc.subject | Cirrhotic-patients | en_US |
dc.subject | Risk | en_US |
dc.subject | Metaanalysis | en_US |
dc.subject | Disorders | en_US |
dc.subject | Mutaion | en_US |
dc.subject | Mthfr | en_US |
dc.subject | Thromboembolism | en_US |
dc.subject | Hematology | en_US |
dc.subject.emtree | 5,10 methylenetetrahydrofolate reductase (FADH2) | en_US |
dc.subject.emtree | Acetylsalicylic acid | en_US |
dc.subject.emtree | Blood clotting factor 5 Leiden | en_US |
dc.subject.emtree | Cardiolipin antibody | en_US |
dc.subject.emtree | Carvedilol | en_US |
dc.subject.emtree | Clopidogrel | en_US |
dc.subject.emtree | Esomeprazole | en_US |
dc.subject.emtree | Homocysteine | en_US |
dc.subject.emtree | Immunoglobulin G antibody | en_US |
dc.subject.emtree | Isosorbide mononitrate | en_US |
dc.subject.emtree | Lansoprazole | en_US |
dc.subject.emtree | Low molecular weight heparin | en_US |
dc.subject.emtree | Nadroparin | en_US |
dc.subject.emtree | Pravastatin | en_US |
dc.subject.emtree | Protein S | en_US |
dc.subject.emtree | Proton pump inhibitor | en_US |
dc.subject.emtree | Acute heart infarction | en_US |
dc.subject.emtree | Adult | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Bleeding | en_US |
dc.subject.emtree | Case report | en_US |
dc.subject.emtree | Cerebrovascular accident | en_US |
dc.subject.emtree | Coronary stent | en_US |
dc.subject.emtree | Drug substitution | en_US |
dc.subject.emtree | Drug withdrawal | en_US |
dc.subject.emtree | Environmental factor | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Gene mutation | en_US |
dc.subject.emtree | Genetic risk | en_US |
dc.subject.emtree | Heterozygosity | en_US |
dc.subject.emtree | Homozygosity | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Percutaneous coronary intervention | en_US |
dc.subject.emtree | Portal vein thrombosis | en_US |
dc.subject.emtree | Portal vein thrombosis | en_US |
dc.subject.emtree | Protein function | en_US |
dc.subject.emtree | Risk factor | en_US |
dc.subject.emtree | Thrombophilia | en_US |
dc.subject.emtree | Thrombosis | en_US |
dc.subject.emtree | Upper gastrointestinal bleeding | en_US |
dc.subject.emtree | Varix bleeding | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Factor V | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Genetic predisposition to disease | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Methylenetetrahydrofolate reductase (nadph2) | en_US |
dc.subject.mesh | Myocardial infarction | en_US |
dc.subject.mesh | Portal vein | en_US |
dc.subject.mesh | Stroke | en_US |
dc.subject.mesh | Thrombophilia | en_US |
dc.subject.mesh | Venous thrombosis | en_US |
dc.subject.scopus | Mutation; Prothrombin; Activated Protein C Resistance | en_US |
dc.subject.wos | Hematology | en_US |
dc.title | Acute myocardial infarction, ischemic cerebrovascular disease and variceal bleeding due to portal vein thrombosis in a patient with hereditary thrombophilia | en_US |
dc.type | Article | en_US |
dc.wos.quartile | Q4 | en_US |
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