BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

215 related articles for article (PubMed ID: 15097012)

  • 1. Maternal and fetal variants of genetic thrombophilias and the risk of preeclampsia.
    Vefring H; Lie RT; ØDegård R; Mansoor MA; Nilsen ST
    Epidemiology; 2004 May; 15(3):317-22. PubMed ID: 15097012
    [TBL] [Abstract][Full Text] [Related]  

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

  • 3. Relationship between polymorphisms in thrombophilic genes and preeclampsia in a Brazilian population.
    Dalmáz CA; Santos KG; Botton MR; Tedoldi CL; Roisenberg I
    Blood Cells Mol Dis; 2006; 37(2):107-10. PubMed ID: 16963292
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Factor V Leiden, pregnancy complications and adverse outcomes: the Hordaland Homocysteine Study.
    Nurk E; Tell GS; Refsum H; Ueland PM; Vollset SE
    QJM; 2006 May; 99(5):289-98. PubMed ID: 16613994
    [TBL] [Abstract][Full Text] [Related]  

  • 5. -455G/A beta-fibrinogen gene polymorphism, factor V Leiden, prothrombin G20210A mutation and MTHFR C677T, and placental vascular complications.
    Camilleri RS; Peebles D; Portmann C; Everington T; Cohen H
    Blood Coagul Fibrinolysis; 2004 Mar; 15(2):139-47. PubMed ID: 15091001
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Fetal genotype for specific inherited thrombophilias is not associated with severe preeclampsia.
    Stanley-Christian H; Ghidini A; Sacher R; Shemirani M
    J Soc Gynecol Investig; 2005 Apr; 12(3):198-201. PubMed ID: 15784506
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ethnic differences in the association of factor V Leiden mutation and the C677T methylenetetrahydrofolate reductase gene polymorphism with preeclampsia.
    Prasmusinto D; Skrablin S; Fimmers R; van der Ven K
    Eur J Obstet Gynecol Reprod Biol; 2004 Feb; 112(2):162-9. PubMed ID: 14746952
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic thrombophilias and preeclampsia: a meta-analysis.
    Lin J; August P
    Obstet Gynecol; 2005 Jan; 105(1):182-92. PubMed ID: 15625161
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Placenta-mediated pregnancy complications are not associated with fetal or paternal factor V Leiden mutation.
    Nevalainen J; Ignatius J; Savolainen ER; Ryynanen M; Jarvenpaa J
    Eur J Obstet Gynecol Reprod Biol; 2018 Nov; 230():32-35. PubMed ID: 30243226
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Methylenetetrahydrofolate reductase C677T polymorphism and Factor V Leiden variant in Mexican women with preeclampsia/eclampsia.
    Dávalos IP; Moran MC; Martínez-Abundis E; González-Ortiz M; Flores-Martínez SE; Machorro V; Sandoval L; Figuera LE; Mena JP; Oliva JM; Tlacuilo-Parra JA; Sánchez-Corona J; Salazar-Páramo M
    Blood Cells Mol Dis; 2005; 35(1):66-9. PubMed ID: 15905108
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prevalence of factor V G1691A (Leiden), prothrombin G20210A, and methylene tetrahydrofolate reductase C677T thrombophilic mutations in children with inflammatory bowel disease.
    Kader HA; Berman WF; Al-Seraihy AS; Ware RE; Ulshen MH; Treem WR
    J Pediatr Gastroenterol Nutr; 2002 Nov; 35(5):629-35. PubMed ID: 12454577
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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; 46(7):10-6. PubMed ID: 18333414
    [TBL] [Abstract][Full Text] [Related]  

  • 14. MTHFR C677T and factor V Leiden in recurrent pregnancy loss: a study among an endogamous group in North India.
    Mukhopadhyay R; Saraswathy KN; Ghosh PK
    Genet Test Mol Biomarkers; 2009 Dec; 13(6):861-5. PubMed ID: 19839754
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous thrombosis.
    Almawi WY; Tamim H; Kreidy R; Timson G; Rahal E; Nabulsi M; Finan RR; Irani-Hakime N
    J Thromb Thrombolysis; 2005 Jun; 19(3):189-96. PubMed ID: 16082606
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Absence of association of thrombophilia polymorphisms with intrauterine growth restriction.
    Infante-Rivard C; Rivard GE; Yotov WV; Génin E; Guiguet M; Weinberg C; Gauthier R; Feoli-Fonseca JC
    N Engl J Med; 2002 Jul; 347(1):19-25. PubMed ID: 12097536
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Preeclampsia in North Indian women: the contribution of genetic polymorphisms.
    Aggarwal S; Dimri N; Tandon I; Agarwal S
    J Obstet Gynaecol Res; 2011 Oct; 37(10):1335-41. PubMed ID: 21564405
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Evaluation of factor V Leiden, prothrombin and methylenetetrahydrofolate reductase gene mutations in patients with severe pregnancy complications in northern Finland.
    Jarvenpaa J; Pakkila M; Savolainen ER; Perheentupa A; Jarvela I; Ryynanen M
    Gynecol Obstet Invest; 2006; 62(1):28-32. PubMed ID: 16514238
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.