175 related articles for article (PubMed ID: 11790575)
1. The PORtromb Project: prothrombin G20210A mutation and venous thromboembolism in young people.
Mansilha A; Araújo F; Sampaio S; Cunha Ribeiro LM; Braga A
Cardiovasc Surg; 2002 Feb; 10(1):45-8. PubMed ID: 11790575
[TBL] [Abstract][Full Text] [Related]
2. The VITA project: prothrombin G20210A mutation and venous thromboembolism in the general population.
Tosetto A; Missiaglia E; Frezzato M; Rodeghiero F
Thromb Haemost; 1999 Nov; 82(5):1395-8. PubMed ID: 10595625
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 11583312
[TBL] [Abstract][Full Text] [Related]
4. Risk of venous thrombosis in carriers of the prothrombin G20210A variant and factor V Leiden and their interaction with oral contraceptives.
Aznar J; Vayá A; Estellés A; Mira Y; Seguí R; Villa P; Ferrando F; Falcó C; Corella D; España F
Haematologica; 2000 Dec; 85(12):1271-6. PubMed ID: 11114134
[TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 17650440
[TBL] [Abstract][Full Text] [Related]
6. Type and location of venous thromboembolism in carriers of Factor V Leiden or prothrombin G20210A mutation versus patients with no mutation.
Kovac M; Mitic G; Mikovic Z; Antonijevic N; Djordjevic V; Mikovic D; Mandic V; Rakicevic L; Radojkovic D
Clin Appl Thromb Hemost; 2010 Feb; 16(1):66-70. PubMed ID: 18796457
[TBL] [Abstract][Full Text] [Related]
7. Phenotypic APC resistance in carriers of the A20210 prothrombin mutation is associated with an increased risk of venous thrombosis.
Castaman G; Tosetto A; Simioni M; Ruggeri M; Madeo D; Rodeghiero F
Thromb Haemost; 2001 Sep; 86(3):804-8. PubMed ID: 11583311
[TBL] [Abstract][Full Text] [Related]
8. The risk of recurrent venous thromboembolism in carriers and non-carriers of the G1691A allele in the coagulation factor V gene and the G20210A allele in the prothrombin gene. DURAC Trial Study Group. Duration of Anticoagulation.
Lindmarker P; Schulman S; Sten-Linder M; Wiman B; Egberg N; Johnsson H
Thromb Haemost; 1999 May; 81(5):684-9. PubMed ID: 10365737
[TBL] [Abstract][Full Text] [Related]
9. Allele 4G of gene PAI-1 associated with prothrombin mutation G20210A increases the risk for venous thrombosis.
Barcellona D; Fenu L; Cauli C; Pisu G; Marongiu F
Thromb Haemost; 2003 Dec; 90(6):1061-4. PubMed ID: 14652637
[TBL] [Abstract][Full Text] [Related]
10. Prothrombin A19911G polymorphism and the risk of venous thromboembolism.
Martinelli I; Battaglioli T; Tosetto A; Legnani C; Sottile L; Ghiotto R; Mannucci PM
J Thromb Haemost; 2006 Dec; 4(12):2582-6. PubMed ID: 16981886
[TBL] [Abstract][Full Text] [Related]
11. Single and combined prothrombotic factors in patients with idiopathic venous thromboembolism: prevalence and risk assessment.
Salomon O; Steinberg DM; Zivelin A; Gitel S; Dardik R; Rosenberg N; Berliner S; Inbal A; Many A; Lubetsky A; Varon D; Martinowitz U; Seligsohn U
Arterioscler Thromb Vasc Biol; 1999 Mar; 19(3):511-8. PubMed ID: 10073951
[TBL] [Abstract][Full Text] [Related]
12. Risk of recurrent venous thrombosis in homozygous carriers and double heterozygous carriers of factor V Leiden and prothrombin G20210A.
Lijfering WM; Middeldorp S; Veeger NJ; Hamulyák K; Prins MH; Büller HR; van der Meer J
Circulation; 2010 Apr; 121(15):1706-12. PubMed ID: 20368522
[TBL] [Abstract][Full Text] [Related]
13. Different circumstances of the first venous thromboembolism among younger or older heterozygous carriers of the G20210A polymorphism in the prothrombin gene.
De Stefano V; Rossi E; Paciaroni K; D'Orazio A; Cina G; Marchitelli E; Pepe R; Leone G
Haematologica; 2003 Jan; 88(1):61-6. PubMed ID: 12551828
[TBL] [Abstract][Full Text] [Related]
14. 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. PubMed ID: 9423788
[TBL] [Abstract][Full Text] [Related]
15. Homozygotes for prothrombin gene 20210 A allele in a thrombophilic family without clinical manifestations of venous thromboembolism.
Souto JC; Mateo J; Soria JM; Llobet D; Coll I; Borrell M; Fontcuberta J
Haematologica; 1999 Jul; 84(7):627-32. PubMed ID: 10406905
[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. Study of the prothrombin gene 20201 GA variant in FV:Q506 carriers in relationship to the presence or absence of juvenile venous thromboembolism.
Ehrenforth S; von Depka Prondsinski M; Aygören-Pürsün E; Nowak-Göttl U; Scharrer I; Ganser A
Arterioscler Thromb Vasc Biol; 1999 Feb; 19(2):276-80. PubMed ID: 9974407
[TBL] [Abstract][Full Text] [Related]
18. Prevalence of the G20210A prothrombin gene mutation in Northwestern Greece and association with venous thromboembolism.
Zalavras ChG; Giotopoulou S; Dokou E; Mitsis M; Ioannou HV; Tsaousi C; Tzolou A; Kolaitis N; Vartholomatos G
Int Angiol; 2003 Mar; 22(1):55-7. PubMed ID: 12771857
[TBL] [Abstract][Full Text] [Related]
19. Impact of the factor II: G20210A variant on the risk of venous thromboembolism in relatives from families with the factor V: R506Q mutation.
Rintelen C; Pabinger I; Bettelheim P; Lechner K; Kyrle PA; Knöbl P; Schneider B; Mannhalter C
Eur J Haematol; 2001 Sep; 67(3):165-9. PubMed ID: 11737249
[TBL] [Abstract][Full Text] [Related]
20. Factor V G1691A and prothrombin G20210A in childhood spontaneous venous thrombosis--evidence of an age-dependent thrombotic onset in carriers of factor V G1691A and prothrombin G20210A mutation.
Schobess R; Junker R; Auberger K; Münchow N; Burdach S; Nowak-Göttl U
Eur J Pediatr; 1999 Dec; 158 Suppl 3():S105-8. PubMed ID: 10650846
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
