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]