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.
123 related articles for article (PubMed ID: 24175756)
21. 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]
22. 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]
23. 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]
24. Combined effect of Factor V Leiden, MTHFR, and angiotensin-converting enzyme (insertion/deletion) gene mutations in hypertensive adult individuals: a population-based study from Sivas and Canakkale, Turkey. Demirel Y; Dogan S; Uludag A; Silan C; Atik S; Silan F; Ozdemir O Genet Test Mol Biomarkers; 2011 Nov; 15(11):785-91. PubMed ID: 21699409 [TBL] [Abstract][Full Text] [Related]
25. Association of retinal vein occlusion, homocysteine, and the thrombophilic mutations in a Turkish population: A case-control study. Koylu MT; Kucukevcilioglu M; Erdurman FC; Durukan AH; Sobacı G; Torun D; Tunca Y; Ayyildiz O Ophthalmic Genet; 2017; 38(4):352-356. PubMed ID: 28085519 [TBL] [Abstract][Full Text] [Related]
26. Prevalence of thrombophilic mutations and ACE I/D polymorphism in Turkish ischemic stroke patients. Celiker G; Can U; Verdi H; Yazici AC; Ozbek N; Atac FB Clin Appl Thromb Hemost; 2009; 15(4):415-20. PubMed ID: 18387982 [TBL] [Abstract][Full Text] [Related]
27. Prevalence of factor V leiden, MTHFR C677T and MTHFR A1298C polymorphisms in patients with deep vein thrombosis in Central Iran. Ehsani M; Imani A; Moravveji A Mol Biol Rep; 2018 Aug; 45(4):621-624. PubMed ID: 29855758 [TBL] [Abstract][Full Text] [Related]
28. Prothrombin polymorphism A19911G, factor V HR2 haplotype A4070G, and plasminogen activator-inhibitor-1 polymorphism 4G/5G and the risk of retinal vein occlusion. Kuhli-Hattenbach C; Hellstern P; Nägler DK; Kohnen T; Hattenbach LO Ophthalmic Genet; 2017; 38(5):413-417. PubMed ID: 28085526 [TBL] [Abstract][Full Text] [Related]
29. Factor V Leiden, prothrombin G20210A, and methylene tetrahydrofolate reductase mutations and stillbirth: the Stillbirth Collaborative Research Network. Silver RM; Saade GR; Thorsten V; Parker CB; Reddy UM; Drews-Botsch C; Conway D; Coustan D; Dudley DJ; Bukowski R; Rowland Hogue CJ; Pinar H; Varner MW; Goldenberg R; Willinger M Am J Obstet Gynecol; 2016 Oct; 215(4):468.e1-468.e17. PubMed ID: 27131585 [TBL] [Abstract][Full Text] [Related]
30. Impact of thrombophilic genes mutations on thrombosis risk in Egyptian nonmetastatic cancer patients. Wahba MA; Ismail MA; Saad AA; Habashy DM; Hafeez ZM; Boshnak NH Blood Coagul Fibrinolysis; 2015 Apr; 26(3):309-15. PubMed ID: 25565385 [TBL] [Abstract][Full Text] [Related]
31. Molecular analysis of factor V Leiden, factor V Hong Kong, factor II G20210A, methylenetetrahydrofolate reductase C677T, and A1298C mutations related to Turkish thrombosis patients. Dölek B; Eraslan S; Eroğlu S; Kesim BE; Ulutin T; Yalçiner A; Laleli YR; Gözükirmizi N Clin Appl Thromb Hemost; 2007 Oct; 13(4):435-8. PubMed ID: 17911197 [TBL] [Abstract][Full Text] [Related]
32. Relationship between polymorphisms in thrombophilic genes and preeclampsia in a Brazilian population. Dalmáz CA; Santos KG; Botton MR; Tedoldi CL; Roisenberg I Blood Cells Mol Dis; 2006; 37(2):107-10. PubMed ID: 16963292 [TBL] [Abstract][Full Text] [Related]
33. Two cousins with neonatal stroke, PAI-1 4G variant and MTHFR A1298C mutation. Golomb MR; Heiny M; Garg BP J Child Neurol; 2007 Jun; 22(6):753-5. PubMed ID: 17641264 [TBL] [Abstract][Full Text] [Related]
34. Do thrombophilic gene mutations have a role on thromboembolic events in cancer patients? Ozkan M; Sivgin S; Kocyigit I; Emirogullari F; Dikilitas M; Kaynar L; Ozkul Y; Er O Asia Pac J Clin Oncol; 2012 Sep; 8(3):e34-41. PubMed ID: 22898008 [TBL] [Abstract][Full Text] [Related]
35. Specific APO E genotypes in combination with the ACE D/D or MTHFR 677TT mutation yield an independent genetic risk of leukoaraiosis. Szolnoki Z; Somogyvári F; Kondacs A; Szabó M; Fodor L; Bene J; Melegh B Acta Neurol Scand; 2004 Mar; 109(3):222-7. PubMed ID: 14763962 [TBL] [Abstract][Full Text] [Related]
36. Contraception-related deep venous thrombosis and pulmonary embolism in a 17-Year-old girl heterozygous for factor V leiden, prothrombin G20210A mutation, MTHFR C677T and homozygous for PAI-1 mutation: report of a family with multiple genetic risk factors and review of the literature. Lenicek Krleza J; Jakovljevic G; Bronic A; Coen Herak D; Bonevski A; Stepan-Giljevic J; Roic G Pathophysiol Haemost Thromb; 2010; 37(1):24-9. PubMed ID: 20664190 [TBL] [Abstract][Full Text] [Related]
37. 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]
38. Renal transplantation experience in a patient with factor V Leiden homozygous, MTHFR C677T heterozygous, and PAI heterozygous mutation. Gülhan B; Tavil B; Gümrük F; Aki TF; Topaloglu R Pediatr Transplant; 2015 Aug; 19(5):E126-9. PubMed ID: 25996881 [TBL] [Abstract][Full Text] [Related]
39. Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy Jordanians. Eid SS; Rihani G Clin Lab Sci; 2004; 17(4):200-2. PubMed ID: 15559724 [TBL] [Abstract][Full Text] [Related]
40. [Prevalence of thrombophilic mutations of FV Leiden, prothrombin G20210A and PAl-1 4G/5G and their combinations in a group of 1450 healthy middle-aged individuals in the Prague and Central Bohemian regions (results of FRET real-time PCR assay)]. Kvasnicka J; Hájková J; Bobcíková P; Kvasnicka T; Dusková D; Poletínová S; Kieferová V Cas Lek Cesk; 2012; 151(2):76-82. PubMed ID: 22515013 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]