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Journal Abstract Search

319 related items for PubMed ID: 16938111

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
    [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
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. [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 Feb; 46(7):10-6. PubMed ID: 18333414
    [Abstract] [Full Text] [Related]

  • 6. Early pregnancy loss in celiac women: The role of genetic markers of thrombophilia.
    Ciacci C, Tortora R, Scudiero O, Di Fiore R, Salvatore F, Castaldo G.
    Dig Liver Dis; 2009 Oct; 41(10):717-20. PubMed ID: 19395327
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. [Patients with inherited trombophilia and recurrent pregnancy loss: incidence].
    Flores-Alatriste JD, Jacobo-Nájera S, Segura-Rodríguez R, Stern-Colin y Nunes JJ.
    Ginecol Obstet Mex; 2014 Jun; 82(6):383-8. PubMed ID: 25016897
    [Abstract] [Full Text] [Related]

  • 9. 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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  • 13. 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 01; 15(2):158-163. PubMed ID: 29703881
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. [Genetic variant C677T in the MTHFR in women with recurrent early fetal loss].
    Ivanov P, Kovacheva K, Komsa-Penkova R, Konova E, Simeonova M, Popov I, Gecheva S, Bozhinova S, Tanchev S, Tsafarov M.
    Akush Ginekol (Sofiia); 2007 Mar 22; 46(4):19-22. PubMed ID: 17974190
    [Abstract] [Full Text] [Related]

  • 16. The 4G/4G polymorphism of the hypofibrinolytic plasminogen activator inhibitor type 1 gene: an independent risk factor for serious pregnancy complications.
    Glueck CJ, Phillips H, Cameron D, Wang P, Fontaine RN, Moore SK, Sieve-Smith L, Tracy T.
    Metabolism; 2000 Jul 22; 49(7):845-52. PubMed ID: 10909993
    [Abstract] [Full Text] [Related]

  • 17. Thrombophilia and unexplained pregnancy loss in Indian patients.
    Vora S, Shetty S, Salvi V, Satoskar P, Ghosh K.
    Natl Med J India; 2008 Jul 22; 21(3):116-9. PubMed ID: 19004141
    [Abstract] [Full Text] [Related]

  • 18. 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 22; 85(4):268-71. PubMed ID: 16450127
    [Abstract] [Full Text] [Related]

  • 19. Double inherited thrombophilias and adverse pregnancy outcomes: fashion or science?
    Larciprete G, Rossi F, Deaibess T, Brienza L, Barbati G, Romanini E, Gioia S, Cirese E.
    J Obstet Gynaecol Res; 2010 Oct 22; 36(5):996-1002. PubMed ID: 20868443
    [Abstract] [Full Text] [Related]

  • 20. 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 Oct 22; 54(77):1438-42. PubMed ID: 17708272
    [Abstract] [Full Text] [Related]

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