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423 related items for PubMed ID: 19133039

  • 1. The prevalence of inherited thrombophilic polymorphisms in an asymptomatic Australian antenatal population.
    Said JM, Brennecke SP, Moses EK, Walker SP, Monagle PT, Campbell J, Bryant VJ, Borg AJ, Higgins JR.
    Aust N Z J Obstet Gynaecol; 2008 Dec; 48(6):536-41. PubMed ID: 19133039
    [Abstract] [Full Text] [Related]

  • 2. Ethnic differences in the prevalence of inherited thrombophilic polymorphisms in an asymptomatic Australian prenatal population.
    Said JM, Brennecke SP, Moses EK, Walker SP, Borg AJ, Williams JT, Higgins JR.
    Hum Biol; 2006 Aug; 78(4):403-12. PubMed ID: 17278618
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  • 3. Inherited thrombophilia polymorphisms and pregnancy outcomes in nulliparous women.
    Said JM, Higgins JR, Moses EK, Walker SP, Borg AJ, Monagle PT, Brennecke SP.
    Obstet Gynecol; 2010 Jan; 115(1):5-13. PubMed ID: 20027027
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  • 4. Inherited thrombophilias and adverse pregnancy outcomes: a case-control study in an Australian population.
    Said JM, Higgins JR, Moses EK, Walker SP, Monagle PT, Brennecke SP.
    Acta Obstet Gynecol Scand; 2012 Feb; 91(2):250-5. PubMed ID: 21985600
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  • 5. Risk of pregnancy-related venous thrombosis in carriers of severe inherited thrombophilia.
    Martinelli I, Legnani C, Bucciarelli P, Grandone E, De Stefano V, Mannucci PM.
    Thromb Haemost; 2001 Sep; 86(3):800-3. PubMed ID: 11583310
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  • 6. [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 Sep; 46(7):10-6. PubMed ID: 18333414
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  • 7. Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy Jordanians.
    Eid SS, Rihani G.
    Clin Lab Sci; 2004 Sep; 17(4):200-2. PubMed ID: 15559724
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  • 8. The prevalence of methylenetetrahydrofolate reductase 677 C-T, factor V 1691 G-A, and prothrombin 20210 G-A mutations in healthy populations in Setif, Algeria.
    Bourouba R, Houcher B, Djabi F, Egin Y, Akar N.
    Clin Appl Thromb Hemost; 2009 Oct; 15(5):529-34. PubMed ID: 18840629
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  • 18. Thrombophilia in infancy: factor V Leiden and MTHFR or factor II double heterozygocity as a risk factor.
    Koren A, Levin C, Hujirat Y, El-Hasid R, Kutai M, Lanir N, Shalev S, Brenner B.
    Pediatr Hematol Oncol; 2003 Oct; 20(3):219-27. PubMed ID: 12637218
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  • 20. Acquired and inherited thrombophilia: implication in recurrent IVF and embryo transfer failure.
    Qublan HS, Eid SS, Ababneh HA, Amarin ZO, Smadi AZ, Al-Khafaji FF, Khader YS.
    Hum Reprod; 2006 Oct; 21(10):2694-8. PubMed ID: 16835215
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