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Journal Abstract Search

294 related items for PubMed ID: 15905108

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  • 3. MTHFR C677T Polymorphism and factor V Leiden mutation are not associated with recurrent spontaneous abortion of unexplained etiology in Japanese women.
    Kobashi G, Kato EH, Morikawa M, Shimada S, Ohta K, Fujimoto S, Minakami H, Yamada H.
    Semin Thromb Hemost; 2005 Jun; 31(3):266-71. PubMed ID: 16052395
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  • 4. Methylenetetrahydrofolate reductase C677T and glutathione S-transferase P1 A313G are associated with a reduced risk of preeclampsia in Maya-Mestizo women.
    Canto P, Canto-Cetina T, Juárez-Velázquez R, Rosas-Vargas H, Rangel-Villalobos H, Canizales-Quinteros S, Velázquez-Wong AC, Villarreal-Molina MT, Fernández G, Coral-Vázquez R.
    Hypertens Res; 2008 May; 31(5):1015-9. PubMed ID: 18712057
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  • 5. Genetic thrombophilias and preeclampsia: a meta-analysis.
    Lin J, August P.
    Obstet Gynecol; 2005 Jan; 105(1):182-92. PubMed ID: 15625161
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  • 10. Association of pre-eclampsia with hyperhomocysteinaemia and methylenetetrahydrofolate reductase gene C677T polymorphism in a Turkish population.
    Yilmaz H, Unlüçerçi Y, Gürdöl F, Isbilen E, Isbir T.
    Aust N Z J Obstet Gynaecol; 2004 Oct; 44(5):423-7. PubMed ID: 15387863
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  • 11. Molecular analysis of factor V Leiden, factor V Hong Kong, factor II G20210A, methylenetetrahydrofolate reductase C677T, and A1298C mutations related to Turkish thrombosis patients.
    Dölek B, Eraslan S, Eroğlu S, Kesim BE, Ulutin T, Yalçiner A, Laleli YR, Gözükirmizi N.
    Clin Appl Thromb Hemost; 2007 Oct; 13(4):435-8. PubMed ID: 17911197
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  • 12. Factor V Leiden, C > T MTHFR polymorphism and genetic susceptibility to preeclampsia.
    Grandone E, Margaglione M, Colaizzo D, Cappucci G, Paladini D, Martinelli P, Montanaro S, Pavone G, Di Minno G.
    Thromb Haemost; 1997 Jun; 77(6):1052-4. PubMed ID: 9241730
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  • 13. Methylenetetrahydrofolate reductase 677 C-->T polymorphism and plasma folate in relation to pre-eclampsia risk among Peruvian women.
    Williams MA, Sanchez SE, Zhang C, Bazul V.
    J Matern Fetal Neonatal Med; 2004 May; 15(5):337-44. PubMed ID: 15280126
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  • 14. 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 May; 54(77):1438-42. PubMed ID: 17708272
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  • 15. The early-onset preeclampsia is associated with MTHFR and FVL polymorphisms.
    Salimi S, Saravani M, Yaghmaei M, Fazlali Z, Mokhtari M, Naghavi A, Farajian-Mashhadi F.
    Arch Gynecol Obstet; 2015 Jun; 291(6):1303-12. PubMed ID: 25480409
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  • 17. 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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  • 18. Inherited thrombophilias and pre-eclampsia in Brazilian women.
    Dusse LM, Carvalho Md, Bragança WF, Paiva SG, Godoi LC, Guimarães DA, Fernandes AP.
    Eur J Obstet Gynecol Reprod Biol; 2007 Sep; 134(1):20-3. PubMed ID: 17097210
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  • 19. Methylenetetrahydrofolate reductase gene, homocysteine and coronary artery disease: the A1298C polymorphism does matter. Inferences from a case study (Madeira, Portugal).
    Freitas AI, Mendonça I, Guerra G, Brión M, Reis RP, Carracedo A, Brehm A.
    Thromb Res; 2008 Sep; 122(5):648-56. PubMed ID: 18384842
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  • 20. Methylenetetrahydrofolate reductase C677T and A1298C polymorphism and changes in homocysteine concentrations in women with idiopathic recurrent pregnancy losses.
    Mtiraoui N, Zammiti W, Ghazouani L, Braham NJ, Saidi S, Finan RR, Almawi WY, Mahjoub T.
    Reproduction; 2006 Feb; 131(2):395-401. PubMed ID: 16452733
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