These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
209 related articles for article (PubMed ID: 17111197)
1. 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]
2. 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]
3. 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]
4. Recurrent pregnancy loss and its relation to combined parental thrombophilic gene mutations. Ozdemir O; Yenicesu GI; Silan F; Köksal B; Atik S; Ozen F; Göl M; Cetin A Genet Test Mol Biomarkers; 2012 Apr; 16(4):279-86. PubMed ID: 22047507 [TBL] [Abstract][Full Text] [Related]
5. Thrombophilic Gene Mutations in Relation to Different Manifestations of Venous Thromboembolism: A Single Tertiary Center Study. Bezgin T; Kaymaz C; Akbal Ö; Yılmaz F; Tokgöz HC; Özdemir N Clin Appl Thromb Hemost; 2018 Jan; 24(1):100-106. PubMed ID: 27729560 [TBL] [Abstract][Full Text] [Related]
6. Comparison of thrombophilic gene mutations among patients experiencing recurrent miscarriage and deep vein thrombosis. Coulam CB; Wallis D; Weinstein J; DasGupta DS; Jeyendran RS Am J Reprod Immunol; 2008 Nov; 60(5):426-31. PubMed ID: 18803625 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. Which thrombophilic gene mutations are risk factors for recurrent pregnancy loss? Goodman CS; Coulam CB; Jeyendran RS; Acosta VA; Roussev R Am J Reprod Immunol; 2006 Oct; 56(4):230-6. PubMed ID: 16938111 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Factor V Leiden G1691A, prothrombin G20210A, and MTHFR C677T mutations in Turkish inflammatory bowel disease patients. Yasa MH; Bolaman Z; Yukselen V; Kadikoylu G; Karaoglul AO; Batun S Hepatogastroenterology; 2007; 54(77):1438-42. PubMed ID: 17708272 [TBL] [Abstract][Full Text] [Related]
13. Multiple thrombophilic gene mutations rather than specific gene mutations are risk factors for recurrent miscarriage. Coulam CB; Jeyendran RS; Fishel LA; Roussev R Am J Reprod Immunol; 2006 May; 55(5):360-8. PubMed ID: 16635210 [TBL] [Abstract][Full Text] [Related]
14. Correlation with Platelet Parameters and Genetic Markers of Thrombophilia Panel (Factor II g.20210G>A, Factor V Leiden, MTHFR (C677T, A1298C), PAI-1, β-Fibrinogen, Factor XIIIA (V34L), Glycoprotein IIIa (L33P)) in Ischemic Strokes. Tasdemir S; Erdem HB; Sahin I; Ozel L; Ozdemir G; Eroz R; Tatar A Neuromolecular Med; 2016 Jun; 18(2):170-6. PubMed ID: 26951304 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Impact of hemostatic gene single point mutations in patients with non-diabetic coronary artery disease. Var A; Utük O; Akçali S; Sanlidağ T; Uyanik BS; Dinç G Mol Biol Rep; 2009 Nov; 36(8):2235-43. PubMed ID: 19123042 [TBL] [Abstract][Full Text] [Related]
18. Association of Polymorphisms in Coagulation Factor Genes and Enzymes of Homocysteine Metabolism With Arterial Ischemic Stroke in Children. Coen Herak D; Lenicek Krleza J; Radic Antolic M; Horvat I; Djuranovic V; Zrinski Topic R; Zadro R Clin Appl Thromb Hemost; 2017 Nov; 23(8):1042-1051. PubMed ID: 28301901 [TBL] [Abstract][Full Text] [Related]
19. Combined germline variations of thrombophilic genes promote genesis of lung cancer. Ozen F; Polat F; Arslan S; Ozdemir O Asian Pac J Cancer Prev; 2013; 14(9):5449-54. PubMed ID: 24175756 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]