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Items: 1 to 20 of 118

1.

Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia.

Makris M, Preston FE, Beauchamp NJ, Cooper PC, Daly ME, Hampton KK, Bayliss P, Peake IR, Miller GJ.

Thromb Haemost. 1997 Dec;78(6):1426-9.

PMID:
9423788
2.

[Prevalence of G20210A prothrombin gene mutation in Poland].

Bykowska K, Vertun-Baranowska B, Windyga J, Łopaciuk S.

Pol Arch Med Wewn. 2000 Nov;104(5):729-33. Polish.

PMID:
11434083
4.

The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease.

Ferraresi P, Marchetti G, Legnani C, Cavallari E, Castoldi E, Mascoli F, Ardissino D, Palareti G, Bernardi F.

Arterioscler Thromb Vasc Biol. 1997 Nov;17(11):2418-22.

5.

The prothrombin gene G20210A variant: prevalence in a U.K. anticoagulant clinic population.

Cumming AM, Keeney S, Salden A, Bhavnani M, Shwe KH, Hay CR.

Br J Haematol. 1997 Aug;98(2):353-5.

PMID:
9266933
6.

Factor V gene (1691A and 4070G) and prothrombin gene 20210A mutations in patients with Behçet's disease.

Ateş A, Düzgün N, Ulu A, Tiryaki AO, Akar N.

Pathophysiol Haemost Thromb. 2003 May-Jun;33(3):157-63.

PMID:
15170396
7.

AB0 blood group and risk of venous or arterial thrombosis in carriers of factor V Leiden or prothrombin G20210A polymorphisms.

Miñano A, Ordóñez A, España F, González-Porras JR, Lecumberri R, Fontcuberta J, Llamas P, Marín F, Estellés A, Alberca I, Vicente V, Corral J.

Haematologica. 2008 May;93(5):729-34. doi: 10.3324/haematol.12271.

8.

The prothrombin gene G20210A variant in an unselected thromboembolic population. A Belgian prospective clinical study.

Hainaut P, Gala JL, Lesage V, Lavenne E, Azerad MA, Zech F, Heusterspreute M, Philippe M, Moriau M.

Acta Clin Belg. 1998 Oct;53(5):344-8.

PMID:
9861761
9.

A patient homozygous for mutation 20210A in the prothrombin gene with venous thrombosis and transient ischemic attacks of thrombotic origin.

González Ordóñez AJ, Medina Rodriguez JM, Fernández Alvarez CR, Macias Robles MD, Coto García E.

Haematologica. 1998 Nov;83(11):1050-1. Review.

10.

Contribution of prothrombin 20210A allele and factor V Leiden mutation to thrombosis risk in thrombophilic families with other hemostatic deficiencies.

Tirado I, Mateo J, Soria JM, Oliver A, Borrell M, Coll I, Vallvé C, Souto JC, Martínez-Sánchez E, Fontcuberta J.

Haematologica. 2001 Nov;86(11):1200-8.

11.

Major and potential prothrombotic genotypes in a cohort of patients with venous thromboembolism.

Varela ML, Adamczuk YP, Forastiero RR, Martinuzzo ME, Cerrato GS, Pombo G, Carreras LO.

Thromb Res. 2001 Dec 1;104(5):317-24.

PMID:
11738073
12.

Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism--pooled analysis of 8 case-control studies including 2310 cases and 3204 controls. Study Group for Pooled-Analysis in Venous Thromboembolism.

Emmerich J, Rosendaal FR, Cattaneo M, Margaglione M, De Stefano V, Cumming T, Arruda V, Hillarp A, Reny JL.

Thromb Haemost. 2001 Sep;86(3):809-16. Erratum in: Thromb Haemost 2001 Dec;86(6):1598.

PMID:
11583312
13.

Prevalence of the prothrombin gene variant (nt20210A) in venous thrombosis and arterial disease.

Arruda VR, Annichino-Bizzacchi JM, Gonçalves MS, Costa FF.

Thromb Haemost. 1997 Dec;78(6):1430-3.

PMID:
9423789
14.

Hereditary thrombophilia and venous thromboembolism.

Murin S, Marelich GP, Arroliga AC, Matthay RA.

Am J Respir Crit Care Med. 1998 Nov;158(5 Pt 1):1369-73. Review.

PMID:
9817680
15.

A prothrombin gene mutation is significantly associated with venous thrombosis.

Kapur RK, Mills LA, Spitzer SG, Hultin MB.

Arterioscler Thromb Vasc Biol. 1997 Nov;17(11):2875-9.

16.

Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant.

Margaglione M, Brancaccio V, Giuliani N, D'Andrea G, Cappucci G, Iannaccone L, Vecchione G, Grandone E, Di Minno G.

Ann Intern Med. 1998 Jul 15;129(2):89-93.

PMID:
9669991
17.

Inherited thrombophilia and first venous thromboembolism during pregnancy and puerperium.

Martinelli I, De Stefano V, Taioli E, Paciaroni K, Rossi E, Mannucci PM.

Thromb Haemost. 2002 May;87(5):791-5.

PMID:
12038778
18.
19.

[Genetic risk factors of thrombosis].

Emmerich J, Aiach M.

Ann Cardiol Angeiol (Paris). 2002 Jun;51(3):129-34. Review. French.

PMID:
12471642
20.

[Genetic thrombophilia and cerebral venous thrombosis].

Romero A, Marco P, Verdú J, Sánchez S, Castaño V.

Med Clin (Barc). 2007 May 5;128(17):655-6. Spanish.

PMID:
17537363
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