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Items: 9

1.

Venous thromboembolic disease and the prothrombin, methylene tetrahydrofolate reductase and factor V genes.

Alhenc-Gelas M, Arnaud E, Nicaud V, Aubry ML, Fiessinger JN, Aiach M, Emmerich J.

Thromb Haemost. 1999 Apr;81(4):506-10.

PMID:
10235429
2.

Interaction between hyperhomocysteinemia and inherited thrombophilic factors in venous thromboembolism.

De Stefano V, Casorelli I, Rossi E, Zappacosta B, Leone G.

Semin Thromb Hemost. 2000;26(3):305-11. Review.

PMID:
11011848
4.

Thrombophilia and venous thromboembolism in pregnancy: a meta-analysis of genetic risk.

Ziakas PD, Poulou LS, Pavlou M, Zintzaras E.

Eur J Obstet Gynecol Reprod Biol. 2015 Aug;191:106-11. doi: 10.1016/j.ejogrb.2015.06.005. Epub 2015 Jun 16. Review.

PMID:
26115054
5.

Recommendations from the EGAPP Working Group: routine testing for Factor V Leiden (R506Q) and prothrombin (20210G>A) mutations in adults with a history of idiopathic venous thromboembolism and their adult family members.

Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Working Group.

Genet Med. 2011 Jan;13(1):67-76. doi: 10.1097/GIM.0b013e3181fbe46f.

PMID:
21150787
6.

The prothrombin 20210 G to A variation and thrombosis.

Bertina RM.

Curr Opin Hematol. 1998 Sep;5(5):339-42. Review.

PMID:
9776213
7.

Novel inherited risk factors for venous thrombosis.

Key NS.

J Lab Clin Med. 1998 Dec;132(6):444-5. Review. No abstract available.

PMID:
9851730
8.

Prothrombin 20209C>T: 16 new cases, association with the 19911A>G polymorphism, and literature review.

Warshawsky I, Makkar V, Rimmerman C, Kottke-Marchant K.

J Thromb Haemost. 2009 Sep;7(9):1585-7. doi: 10.1111/j.1538-7836.2009.03513.x. Epub 2009 Jun 9. Review. No abstract available.

9.

Methylene tetrahydrofolate reductase gene and coronary artery disease.

Iqbal MP, Frossard PM.

J Pak Med Assoc. 2003 Jan;53(1):33-6. Review. No abstract available.

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