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Journal Abstract Search

351 related items for PubMed ID: 12042290

  • 1. Prevalence of genetic markers for thrombophilia in recurrent pregnancy loss.
    Carp H, Salomon O, Seidman D, Dardik R, Rosenberg N, Inbal A.
    Hum Reprod; 2002 Jun; 17(6):1633-7. PubMed ID: 12042290
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  • 2. [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 Jun; 46(7):10-6. PubMed ID: 18333414
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  • 3. Factor V leiden and prothrombin G20210A mutations, but not methylenetetrahydrofolate reductase C677T, are associated with recurrent miscarriages.
    Foka ZJ, Lambropoulos AF, Saravelos H, Karas GB, Karavida A, Agorastos T, Zournatzi V, Makris PE, Bontis J, Kotsis A.
    Hum Reprod; 2000 Feb; 15(2):458-62. PubMed ID: 10655323
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  • 7. Plasminogen activator inhibitor-1, factor V, factor II and methylenetetrahydrofolate reductase polymorphisms in women with recurrent miscarriage.
    Pietropolli A, Giuliani E, Bruno V, Patrizi L, Piccione E, Ticconi C.
    J Obstet Gynaecol; 2014 Apr; 34(3):229-34. PubMed ID: 24484533
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  • 9. 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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  • 13. Analyzes of three common thrombophilic gene mutations in German women with recurrent abortions.
    Pauer HU, Voigt-Tschirschwitz T, Hinney B, Burfeind P, Wolf C, Emons G, Neesen J.
    Acta Obstet Gynecol Scand; 2003 Oct; 82(10):942-7. PubMed ID: 12956845
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  • 14. Association between FVL G1691A, FII G20210A, and MTHFR C677T and A1298C polymorphisms and Turkish women with recurrent pregnancy loss.
    Yengel I, Yorulmaz T, Api M.
    Med Glas (Zenica); 2020 Feb 01; 17(1):129-135. PubMed ID: 31994856
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  • 16. Risk Factors of Thrombophilia-Related Mutations for Early and Late Pregnancy Loss.
    Borsi E, Potre O, Ionita I, Samfireag M, Secosan C, Potre C.
    Medicina (Kaunas); 2024 Mar 22; 60(4):. PubMed ID: 38674167
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  • 17. Inherited thrombophilia with recurrent pregnancy loss in Turkish women--a real phenomenon?
    Yildiz G, Yavuzcan A, Yildiz P, Süer N, Tandoğan N.
    Ginekol Pol; 2012 Aug 22; 83(8):598-603. PubMed ID: 23342883
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  • 18. Thrombophilic genes alterations as risk factor for recurrent pregnancy loss.
    Farahmand K, Totonchi M, Hashemi M, Reyhani Sabet F, Kalantari H, Gourabi H, Mohseni Meybodi A.
    J Matern Fetal Neonatal Med; 2016 Aug 22; 29(8):1269-73. PubMed ID: 26135458
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  • 19. Prevalence of factor V G1691A (Leiden), prothrombin G20210A, and methylene tetrahydrofolate reductase C677T thrombophilic mutations in children with inflammatory bowel disease.
    Kader HA, Berman WF, Al-Seraihy AS, Ware RE, Ulshen MH, Treem WR.
    J Pediatr Gastroenterol Nutr; 2002 Nov 22; 35(5):629-35. PubMed ID: 12454577
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  • 20. Prothrombin and factor V mutations in women with a history of thrombosis during pregnancy and the puerperium.
    Gerhardt A, Scharf RE, Beckmann MW, Struve S, Bender HG, Pillny M, Sandmann W, Zotz RB.
    N Engl J Med; 2000 Feb 10; 342(6):374-80. PubMed ID: 10666427
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