741 related articles for article (PubMed ID: 19906129)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. [Genetic thrombophilic defects (Factor V Leiden, prothrombin G20210A, MTHFR C677T) in women with recurrent fetal loss].
Kovacheva K; Ivanov P; Konova E; Simeonova M; Komsa-Penkova R
Akush Ginekol (Sofiia); 2007; 46(7):10-6. PubMed ID: 18333414
[TBL] [Abstract][Full Text] [Related]
7. Genetic thrombophilic mutations among couples with recurrent miscarriage.
Jivraj S; Rai R; Underwood J; Regan L
Hum Reprod; 2006 May; 21(5):1161-5. PubMed ID: 16431900
[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. Factor V Leiden and G20210A prothrombin mutations in patients with recurrent pregnancy loss: data from the southeast of Turkey.
Altintas A; Pasa S; Akdeniz N; Cil T; Yurt M; Ayyildiz O; Batun S; Isi H
Ann Hematol; 2007 Oct; 86(10):727-31. PubMed ID: 17572893
[TBL] [Abstract][Full Text] [Related]
10. Thrombophilic gene polymorphisms and recurrent pregnancy loss in Greek women.
Chatzidimitriou M; Chatzidimitriou D; Mavridou M; Anetakis C; Chatzopoulou F; Lialiaris T; Mitka S
Int J Lab Hematol; 2017 Dec; 39(6):590-595. PubMed ID: 28603947
[TBL] [Abstract][Full Text] [Related]
11. Combined thrombophilic mutations in women with unexplained recurrent miscarriage.
Sotiriadis A; Vartholomatos G; Pavlou M; Kolaitis N; Dova L; Stefos T; Paraskevaidis E; Kalantaridou SN
Am J Reprod Immunol; 2007 Feb; 57(2):133-41. PubMed ID: 17217367
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. Analysis of plasminogen activator inhibitor-1, integrin beta3, beta fibrinogen, and methylenetetrahydrofolate reductase polymorphisms in Iranian women with recurrent pregnancy loss.
Jeddi-Tehrani M; Torabi R; Zarnani AH; Mohammadzadeh A; Arefi S; Zeraati H; Akhondi MM; Chamani-Tabriz L; Idali F; Emami S; Zarei S
Am J Reprod Immunol; 2011 Aug; 66(2):149-56. PubMed ID: 21241403
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. The frequency of factor V Leiden and concomitance of factor V Leiden with prothrombin G20210A mutation and methylene tetrahydrofolate reductase C677T gene mutation in healthy population of Denizli, Aegean region of Turkey.
Kabukcu S; Keskin N; Keskin A; Atalay E
Clin Appl Thromb Hemost; 2007 Apr; 13(2):166-71. PubMed ID: 17456626
[TBL] [Abstract][Full Text] [Related]
18. Paternal thrombophilic gene mutations are not associated with recurrent miscarriage.
Toth B; Vocke F; Rogenhofer N; Friese K; Thaler CJ; Lohse P
Am J Reprod Immunol; 2008 Oct; 60(4):325-32. PubMed ID: 18754836
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Thrombophilic mutations in Iranian patients with infertility and recurrent spontaneous abortion.
Behjati R; Modarressi MH; Jeddi-Tehrani M; Dokoohaki P; Ghasemi J; Zarnani AH; Aarabi M; Memariani T; Ghaffari M; Akhondi MA
Ann Hematol; 2006 Apr; 85(4):268-71. PubMed ID: 16450127
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]