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Journal Abstract Search

339 related items for PubMed ID: 18957855

  • 21. Thrombophilic mutations are a main risk factor for placental abruption.
    Facchinetti F, Marozio L, Grandone E, Pizzi C, Volpe A, Benedetto C.
    Haematologica; 2003 Jul; 88(7):785-8. PubMed ID: 12857557
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  • 23. Prevalence of factor V Leiden, prothrombin and methylene tetrahydrofolate reductase mutations in women with adverse pregnancy outcomes in Lebanon.
    Zahed LF, Rayes RF, Mahfouz RA, Taher AT, Maarouf HH, Nassar AH.
    Am J Obstet Gynecol; 2006 Oct; 195(4):1114-8. PubMed ID: 17000243
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  • 24. Increased rates of thrombophilia in women with repeated IVF failures.
    Azem F, Many A, Ben Ami I, Yovel I, Amit A, Lessing JB, Kupferminc MJ.
    Hum Reprod; 2004 Feb; 19(2):368-70. PubMed ID: 14747183
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  • 25. Thrombophilic gene polymorphisms are risk factors for unexplained infertility.
    Coulam CB, Jeyendran RS.
    Fertil Steril; 2009 Apr; 91(4 Suppl):1516-7. PubMed ID: 18930220
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  • 26. 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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  • 27. [THROMBOPHILIC GENETIC MUTATIONS AND POLYMORPHISMS IN WOMEN WITH INFERTILITY AND FAILED IN VITRO FERTILIZATION].
    Abrahamyan G.
    Georgian Med News; 2017 Apr; (268-269):28-34. PubMed ID: 28820408
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  • 29. Diagnostic evaluation of women experiencing repeated in vitro fertilization failure.
    Vaquero E, Lazzarin N, Caserta D, Valensise H, Baldi M, Moscarini M, Arduini D.
    Eur J Obstet Gynecol Reprod Biol; 2006 Mar 01; 125(1):79-84. PubMed ID: 16223559
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  • 30. [Relationship between three thrombophilic gene mutations and unexplained recurrent early spontaneous abortion].
    Xu L, Liu XM, Zhang HY, Zhao J, Qi QW, Chang YF.
    Zhonghua Fu Chan Ke Za Zhi; 2007 Mar 01; 42(3):180-3. PubMed ID: 17537304
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  • 31. 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 01; 86(10):727-31. PubMed ID: 17572893
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  • 32. Third trimester nonrecurrent fetal loss is associated with factor V Leiden and prothrombin gene mutations.
    Karateke A, Haliloglu B, Gurbuz A.
    J Matern Fetal Neonatal Med; 2005 Nov 01; 18(5):299-304. PubMed ID: 16390788
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  • 34. Obstetric complications in patients with hereditary thrombophilia identified using the LCx microparticle enzyme immunoassay: a controlled study of 5,000 patients.
    Kocher O, Cirovic C, Malynn E, Rowland CM, Bare LA, Young BA, Henslee JG, Laffler TG, Huff JB, Kruskall MS, Wong G, Bauer KA.
    Am J Clin Pathol; 2007 Jan 01; 127(1):68-75. PubMed ID: 17145624
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  • 35. 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 Jan 01; 54(77):1438-42. PubMed ID: 17708272
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  • 36. Association of common thrombophilias and antiphospholipid antibodies with success rate of in vitro fertilisation.
    Steinvil A, Raz R, Berliner S, Steinberg DM, Zeltser D, Levran D, Shimron O, Sella T, Chodick G, Shalev V, Salomon O.
    Thromb Haemost; 2012 Dec 01; 108(6):1192-7. PubMed ID: 23052827
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  • 39. 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 01; 60(5):426-31. PubMed ID: 18803625
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