194 related articles for article (PubMed ID: 32633259)
1. The effects of genetic polymorphisms and diabetes mellitus on the development of peripheral artery disease.
Yalım Z; Tutgun Onrat S; Alan S; Aldemir M; Avşar A; Doğan İ; Onrat E
Turk Kardiyol Dern Ars; 2020 Jul; 48(5):484-493. PubMed ID: 32633259
[TBL] [Abstract][Full Text] [Related]
2. Genetic polymorphisms associated with retinal vein occlusion: a Greek case-control study and meta-analysis.
Yioti GG; Panagiotou OA; Vartholomatos GA; Kolaitis NI; Pappa CN; Evangelou E; Stefaniotou MI
Ophthalmic Genet; 2013 Sep; 34(3):130-9. PubMed ID: 23289804
[TBL] [Abstract][Full Text] [Related]
3. Evaluation of Factor V G1691A, prothrombin G20210A, Factor XIII V34L, MTHFR A1298C, MTHFR C677T and PAI-1 4G/5G genotype frequencies of patients subjected to cardiovascular disease (CVD) panel in south-east region of Turkey.
Oztuzcu S; Ergun S; Ulaşlı M; Nacarkahya G; Iğci YZ; Iğci M; Bayraktar R; Tamer A; Çakmak EA; Arslan A
Mol Biol Rep; 2014 Jun; 41(6):3671-6. PubMed ID: 24532105
[TBL] [Abstract][Full Text] [Related]
4. A prospective case-control study analyzes 12 thrombophilic gene mutations in Turkish couples with recurrent pregnancy loss.
Yenicesu GI; Cetin M; Ozdemir O; Cetin A; Ozen F; Yenicesu C; Yildiz C; Kocak N
Am J Reprod Immunol; 2010 Feb; 63(2):126-36. PubMed ID: 19906129
[TBL] [Abstract][Full Text] [Related]
5. Analysis of inherited thrombophilic mutations and natural anticoagulant deficiency in patients with idiopathic portal hypertension.
Bayan K; Tüzün Y; Yilmaz S; Canoruc N; Dursun M
J Thromb Thrombolysis; 2009 Jul; 28(1):57-62. PubMed ID: 18685811
[TBL] [Abstract][Full Text] [Related]
6. Risk Factors of Thrombophilia-Related Mutations for Early and Late Pregnancy Loss.
Borsi E; Potre O; Ionita I; Samfireag M; Secosan C; Potre C
Medicina (Kaunas); 2024 Mar; 60(4):. PubMed ID: 38674167
[No Abstract] [Full Text] [Related]
7. Analysis of thrombophilic genetic mutations in patients with Sheehan's syndrome: is thrombophilia responsible for the pathogenesis of Sheehan's syndrome?
Gokalp D; Tuzcu A; Bahceci M; Ayyildiz O; Yurt M; Celik Y; Alpagat G
Pituitary; 2011 Jun; 14(2):168-73. PubMed ID: 21107737
[TBL] [Abstract][Full Text] [Related]
8. The association of factor V G1961A (factor V Leiden), prothrombin G20210A, MTHFR C677T and PAI-1 4G/5G polymorphisms with recurrent pregnancy loss in Bosnian women.
Jusić A; Balić D; Avdić A; Pođanin M; Balić A
Med Glas (Zenica); 2018 Aug; 15(2):158-163. PubMed ID: 29703881
[TBL] [Abstract][Full Text] [Related]
9. Variant alleles in factor V, prothrombin, plasminogen activator inhibitor-1, methylenetetrahydrofolate reductase and risk of thromboembolism in metastatic colorectal cancer patients treated with first-line chemotherapy plus bevacizumab.
Falvella FS; Cremolini C; Miceli R; Nichetti F; Cheli S; Antoniotti C; Infante G; Martinetti A; Marmorino F; Sottotetti E; Berenato R; Caporale M; Colombo A; de Braud F; Di Bartolomeo M; Clementi E; Loupakis F; Pietrantonio F
Pharmacogenomics J; 2017 Jul; 17(4):331-336. PubMed ID: 27001121
[TBL] [Abstract][Full Text] [Related]
10. Factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations are not associated with chronic limb ischemia: the Linz Peripheral Arterial Disease (LIPAD) study.
Mueller T; Marschon R; Dieplinger B; Haidinger D; Gegenhuber A; Poelz W; Webersinke G; Haltmayer M
J Vasc Surg; 2005 May; 41(5):808-15. PubMed ID: 15886665
[TBL] [Abstract][Full Text] [Related]
11. Genetic polymorphisms associated with thrombophilia and vascular disease in women with unexplained late intrauterine fetal death: a multicenter study.
Hefler L; Jirecek S; Heim K; Grimm C; Antensteiner G; Zeillinger R; Husslein P; Tempfer C
J Soc Gynecol Investig; 2004 Jan; 11(1):42-4. PubMed ID: 14706682
[TBL] [Abstract][Full Text] [Related]
12. Analysis of thrombophilic gene mutations in coronary artery ectasia.
Yalım Z; Tutgun Onrat S; Emren SV; Dural İE; Avşar A; Onrat E
Turk Kardiyol Dern Ars; 2020 Jun; 48(4):368-373. PubMed ID: 32525847
[TBL] [Abstract][Full Text] [Related]
13. Plasminogen activator inhibitor-1, factor V, factor II and methylenetetrahydrofolate reductase polymorphisms in women with recurrent miscarriage.
Pietropolli A; Giuliani E; Bruno V; Patrizi L; Piccione E; Ticconi C
J Obstet Gynaecol; 2014 Apr; 34(3):229-34. PubMed ID: 24484533
[TBL] [Abstract][Full Text] [Related]
14. Genetic factors associated with the predisposition to late onset Alzheimer's disease.
Durmaz A; Kumral E; Durmaz B; Onay H; Aslan GI; Ozkinay F; Pehlivan S; Orman M; Cogulu O
Gene; 2019 Jul; 707():212-215. PubMed ID: 31102717
[TBL] [Abstract][Full Text] [Related]
15. Association between plasminogen activator inhibitor 1 gene polymorphisms and preeclampsia.
Fabbro D; D'Elia AV; Spizzo R; Driul L; Barillari G; Di Loreto C; Marchesoni D; Damante G
Gynecol Obstet Invest; 2003; 56(1):17-22. PubMed ID: 12867763
[TBL] [Abstract][Full Text] [Related]
16. A comprehensive analysis of 12 thrombophilic mutations and related parameters in patients with inflammatory bowel disease: data from Turkey.
Yilmaz S; Bayan K; Tüzün Y; Batun S; Altintaş A
J Thromb Thrombolysis; 2006 Dec; 22(3):205-12. PubMed ID: 17111197
[TBL] [Abstract][Full Text] [Related]
17. Polymorphisms in prothrombotic genes in young stroke patients in Greece: a case-controlled study.
Ranellou K; Paraskeva A; Kyriazopoulos P; Batistatou A; Evangelou A; El-Aly M; Zis P; Tavernarakis A; Charalabopoulos K
Blood Coagul Fibrinolysis; 2015 Jun; 26(4):430-5. PubMed ID: 25699610
[TBL] [Abstract][Full Text] [Related]
18. Factor V Leiden, prothrombin, MTHFR, and PAI-1 gene polymorphisms in patients with arterial disease: A comprehensive systematic-review and meta-analysis.
Valeriani E; Pastori D; Astorri G; Porfidia A; Menichelli D; Pignatelli P
Thromb Res; 2023 Oct; 230():74-83. PubMed ID: 37643522
[TBL] [Abstract][Full Text] [Related]
19. Combined Effect of MTHFR C677T and PAI-1 4G/5G Polymorphisms on the Risk of Venous Thromboembolism in Chinese Lung Cancer Patients.
Wang B; Xu P; Shu Q; Yan S; Xu H
Clin Appl Thromb Hemost; 2021; 27():10760296211031291. PubMed ID: 34325549
[TBL] [Abstract][Full Text] [Related]
20. Association of deep venous thrombosis with prothrombotic gene polymorphism identified in lung cancer cases.
Arslan S; Manduz S; Epöztürk K; Karahan O; Akkurt I
Mol Biol Rep; 2011 Apr; 38(4):2395-400. PubMed ID: 21080081
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
