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Journal Abstract Search

213 related items for PubMed ID: 10456445

  • 1. Thrombophilic polymorphisms are common in women with fetal loss without apparent cause.
    Brenner B, Sarig G, Weiner Z, Younis J, Blumenfeld Z, Lanir N.
    Thromb Haemost; 1999 Jul; 82(1):6-9. PubMed ID: 10456445
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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 Jul; 46(7):10-6. PubMed ID: 18333414
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  • 3. Case-control study of the frequency of thrombophilic disorders in couples with late foetal loss and no thrombotic antecedent--the Nîmes Obstetricians and Haematologists Study5 (NOHA5).
    Gris JC, Quéré I, Monpeyroux F, Mercier E, Ripart-Neveu S, Tailland ML, Hoffet M, Berlan J, Daurès JP, Marès P.
    Thromb Haemost; 1999 Jun; 81(6):891-9. PubMed ID: 10404763
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  • 4. 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; 18(5):299-304. PubMed ID: 16390788
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  • 5. 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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  • 7. Factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T are not associated with coronary artery disease and type 2 diabetes mellitus in western Iran.
    Rahimi Z, Nomani H, Mozafari H, Vaisi-Raygani A, Madani H, Malek-Khosravi S, Parsian A.
    Blood Coagul Fibrinolysis; 2009 Jun; 20(4):252-6. PubMed ID: 19349859
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  • 9. The platelet glycoprotein Ia/IIa gene polymorphism C807T/G873A: a novel risk factor for retinal vein occlusion.
    Dodson PM, Haynes J, Starczynski J, Farmer J, Shigdar S, Fegan G, Johnson RJ, Fegan C.
    Eye (Lond); 2003 Aug; 17(6):772-7. PubMed ID: 12928694
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  • 10. Effects of factor V gene G1691A, methylenetetrahydrofolate reductase gene C677T, and prothombin gene G20210A mutations on deep venous thrombogenesis in Behçet's disease.
    Toydemir PB, Elhan AH, Tükün A, Toydemir R, Gürler A, Tüzüner A, Bökesoy I.
    J Rheumatol; 2000 Dec; 27(12):2849-54. PubMed ID: 11128675
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  • 12. Thrombophilia and unexplained pregnancy loss in Indian patients.
    Vora S, Shetty S, Salvi V, Satoskar P, Ghosh K.
    Natl Med J India; 2008 Dec; 21(3):116-9. PubMed ID: 19004141
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  • 19. Maternal and fetal inherited thrombophilias are not related to the development of severe preeclampsia.
    Livingston JC, Barton JR, Park V, Haddad B, Phillips O, Sibai BM.
    Am J Obstet Gynecol; 2001 Jul; 185(1):153-7. PubMed ID: 11483920
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  • 20. Embryo implantation after assisted reproductive procedures and maternal thrombophilia.
    Martinelli I, Taioli E, Ragni G, Levi-Setti P, Passamonti SM, Battaglioli T, Lodigiani C, Mannucci PM.
    Haematologica; 2003 Jul; 88(7):789-93. PubMed ID: 12857558
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