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Journal Abstract Search

946 related items for PubMed ID: 16635210

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  • 23. Inherited thrombophilia in infertile women: implication in unexplained infertility.
    Casadei L, Puca F, Privitera L, Zamaro V, Emidi E.
    Fertil Steril; 2010 Jul; 94(2):755-7. PubMed ID: 19939360
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  • 24. 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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  • 27. Hereditary thrombophilia, anti-beta2 glycoprotein 1 IgM, and anti-annexin V antibodies in recurrent pregnancy loss.
    Karata S, Aydin Y, Ocer F, Buyru A, Balci H.
    Am J Reprod Immunol; 2012 Mar 22; 67(3):251-5. PubMed ID: 22103678
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  • 28. 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 Mar 22; 54(77):1438-42. PubMed ID: 17708272
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  • 29. 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 22; 34(3):229-34. PubMed ID: 24484533
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  • 33. [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 22; 82(6):383-8. PubMed ID: 25016897
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  • 35. Association between adverse pregnancy outcomes and maternal factor V G1691A (Leiden) and prothrombin G20210A genotypes in women with a history of recurrent idiopathic miscarriages.
    Mahjoub T, Mtiraoui N, Tamim H, Hizem S, Finan RR, Nsiri B, Almawi WY.
    Am J Hematol; 2005 Sep 22; 80(1):12-9. PubMed ID: 16138341
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  • 38. 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 22; 86(10):727-31. PubMed ID: 17572893
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  • 39. Evaluation of chromosomal abnormalities and common trombophilic mutations in cases with recurrent miscarriage.
    Karatas A, Eroz R, Albayrak M, Ozlu T, Cakmak B, Keskin F.
    Afr Health Sci; 2014 Mar 22; 14(1):216-22. PubMed ID: 26060483
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