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Journal Abstract Search

745 related items for 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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 Aug; 54(77):1438-42. PubMed ID: 17708272
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  • 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
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  • 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
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  • 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
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  • 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
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