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Results: 8

1.

Clinical studies and thrombin generation in patients homozygous or heterozygous for the G20210A mutation in the prothrombin gene.

Kyrle PA, Mannhalter C, Béguin S, Stümpflen A, Hirschl M, Weltermann A, Stain M, Brenner B, Speiser W, Pabinger I, Lechner K, Eichinger S.

Arterioscler Thromb Vasc Biol. 1998 Aug;18(8):1287-91.

PMID:
9714136
[PubMed - indexed for MEDLINE]
Free Article
2.

The risk of recurrent venous thromboembolism among heterozygous carriers of factor V Leiden or prothrombin G20210A mutation. A systematic review of prospective studies.

Marchiori A, Mosena L, Prins MH, Prandoni P.

Haematologica. 2007 Aug;92(8):1107-14. Review.

PMID:
17650440
[PubMed - indexed for MEDLINE]
Free Article
3.

[G20210A transition in the prothrombin gene and venous thromboembolic disease].

Trillot N, Zawadzki C, Watel A, Jude B.

Rev Med Interne. 2000 Oct;21(10):911-4. Review. French.

PMID:
11075405
[PubMed - indexed for MEDLINE]
4.

Effects of oral contraceptives on hemostasis and thrombosis.

Rosing J, Tans G.

Am J Obstet Gynecol. 1999 Jun;180(6 Pt 2):S375-82. Review.

PMID:
10368524
[PubMed - indexed for MEDLINE]
5.

Thrombin generation in plasma: its assessment via the endogenous thrombin potential.

Hemker HC, Béguin S.

Thromb Haemost. 1995 Jul;74(1):134-8. Review. Erratum in: Thromb Haemost 1995 Nov;74(5):1388.

PMID:
8578446
[PubMed - indexed for MEDLINE]
6.

Clinical relevance of protein C.

Pabinger I.

Blut. 1986 Aug;53(2):63-75. Review.

PMID:
3524711
[PubMed - indexed for MEDLINE]
7.

Congenital prothrombin deficiency.

Lancellotti S, De Cristofaro R.

Semin Thromb Hemost. 2009 Jun;35(4):367-81. doi: 10.1055/s-0029-1225759. Epub 2009 Jul 13. Review.

PMID:
19598065
[PubMed - indexed for MEDLINE]
8.

Congenital prothrombin deficiency: an update.

Lancellotti S, Basso M, De Cristofaro R.

Semin Thromb Hemost. 2013 Sep;39(6):596-606. doi: 10.1055/s-0033-1348948. Epub 2013 Jul 12. Review.

PMID:
23852823
[PubMed - indexed for MEDLINE]
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