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Items: 1 to 20 of 93

1.

Polymorphisms in thrombophilia and renin-angiotensin system pathways, preterm delivery, and evidence of placental hemorrhage.

Gargano JW, Holzman CB, Senagore PK, Reuss ML, Pathak DR, Friderici KH, Jernigan K, Fisher R.

Am J Obstet Gynecol. 2009 Sep;201(3):317.e1-9. doi: 10.1016/j.ajog.2009.05.060.

2.

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. doi: 10.1097/AOG.0b013e3181c68907.

PMID:
20027027
3.

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. Epub 2006 Apr 13.

PMID:
16613994
4.

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. doi: 10.1111/j.1447-0756.2010.01523.x. Epub 2011 May 12.

PMID:
21564405
5.

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.

PMID:
15097012
6.

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. doi: 10.1007/s00404-014-3561-5. Epub 2014 Dec 6.

PMID:
25480409
7.

Associations between 2 polymorphisms in the methylenetetrahydrofolate reductase gene and placental abruption.

Ananth CV, Peltier MR, De Marco C, Elsasser DA, Getahun D, Rozen R, Smulian JC; New Jersey-Placental Abruption Study Investigators..

Am J Obstet Gynecol. 2007 Oct;197(4):385.e1-7.

8.

Thrombophilic polymorphisms--factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations--and preterm birth.

Resch B, Gallistl S, Kutschera J, Mannhalter C, Muntean W, Mueller WD.

Wien Klin Wochenschr. 2004 Sep 30;116(17-18):622-6.

PMID:
15515881
9.

Frequency of selected thrombophilias in women with placental abruption.

Procházka M, Lubuský M, Slavík L, Hrachovec P, Zielina P, Kudela M, Lindqvist PG.

Aust N Z J Obstet Gynaecol. 2007 Aug;47(4):297-301.

PMID:
17627684
10.

Thrombophilic polymorphisms in preterm delivery.

Valdez LL, Quintero A, Garcia E, Olivares N, Celis A, Rivas F Jr, Rivas F.

Blood Cells Mol Dis. 2004 Jul-Aug;33(1):51-6.

PMID:
15223011
11.

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 Sep-Oct;37(2):107-10. Epub 2006 Sep 11.

PMID:
16963292
12.

Influence of renin-angiotensin system gene polymorphisms on the risk of ST-segment-elevation myocardial infarction and association with coronary artery disease risk factors.

Konopka A, Szperl M, Piotrowski W, Roszczynko M, Stępińska J.

Mol Diagn Ther. 2011 Jun 1;15(3):167-76. doi: 10.2165/11590650-000000000-00000.

PMID:
21657802
13.

Association of methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism with preterm delivery and placental abruption: a systematic review and meta-analysis.

Chen J, Chen L, Zhu LH, Zhang ST, Wu YL.

Acta Obstet Gynecol Scand. 2016 Feb;95(2):157-65. doi: 10.1111/aogs.12789. Epub 2015 Nov 6. Review.

PMID:
26439908
14.
15.

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. doi: 10.1089/gtmb.2009.0063.

PMID:
19839754
16.

-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.

PMID:
15091001
17.

The association of factor V leiden and prothrombin gene mutation and placenta-mediated pregnancy complications: a systematic review and meta-analysis of prospective cohort studies.

Rodger MA, Betancourt MT, Clark P, Lindqvist PG, Dizon-Townson D, Said J, Seligsohn U, Carrier M, Salomon O, Greer IA.

PLoS Med. 2010 Jun 15;7(6):e1000292. doi: 10.1371/journal.pmed.1000292. Review.

18.

The role of point mutations in the genes, predisposing inherited thrombophilia in the pathogeneses of proximal and distal deep vein thrombosis in Georgian population.

Pirtskhelani N, Kochiashvili N, Makhaldiani L, Pargalava N, Gaprindashvili E, Kartvelishvili K.

Georgian Med News. 2014 Feb;(227):98-102.

PMID:
24632657
19.

Plasminogen activator inhibitor-1, factor V, factor II and methylenetetrahydrofolate reductase polymorphisms in women with recurrent miscarriage.

Pietropolli A, Giuliani E, Bruno V, Patrizi L, Piccione E, Ticconi C.

J Obstet Gynaecol. 2014 Apr;34(3):229-34. doi: 10.3109/01443615.2013.836476. Epub 2014 Jan 31.

PMID:
24484533
20.

Genetic polymorphisms of the renin-angiotensin system in preterm delivery and premature rupture of membranes.

Valdez-Velazquez LL, Quintero-Ramos A, Perez SA, Mendoza-Carrera F, Montoya-Fuentes H, Rivas F Jr, Olivares N, Celis A, Vazquez OF, Rivas F.

J Renin Angiotensin Aldosterone Syst. 2007 Dec;8(4):160-8. doi: 10.3317/jraas.2007.026.

PMID:
18205094

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