219 related articles for article (PubMed ID: 9974407)
21. 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]
22. 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. PubMed ID: 18387978
[TBL] [Abstract][Full Text] [Related]
23. Methylenetetrahydrofolate reductase C677T genotype and venous thromboembolic disease.
Couturaud F; Oger E; Abalain JH; Chenu E; Guias B; Floch HH; Mercier B; Mottier D; Leroyer C
Respiration; 2000; 67(6):657-61. PubMed ID: 11124649
[TBL] [Abstract][Full Text] [Related]
24. The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation.
Margaglione M; D'Andrea G; d'Addedda M; Giuliani N; Cappucci G; Iannaccone L; Vecchione G; Grandone E; Brancaccio V; Di Minno G
Thromb Haemost; 1998 May; 79(5):907-11. PubMed ID: 9609218
[TBL] [Abstract][Full Text] [Related]
25. The risk of first venous thromboembolism during pregnancy and puerperium in double heterozygotes for factor V Leiden and prothrombin G20210A.
Martinelli I; Battaglioli T; De Stefano V; Tormene D; Valdrè L; Grandone E; Tosetto A; Mannucci PM;
J Thromb Haemost; 2008 Mar; 6(3):494-8. PubMed ID: 18182035
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Prevalence and association of the factor V Leiden and prothrombin G20210A in healthy subjects and patients with venous thromboembolism.
Coen D; Zadro R; Honović L; Banfić L; Stavljenić Rukavina A
Croat Med J; 2001 Aug; 42(4):488-92. PubMed ID: 11471205
[TBL] [Abstract][Full Text] [Related]
28. Thrombin generation and D-dimer concentrations in a patient cohort investigated for venous thromboembolism. Relations to venous thrombosis, factor V Leiden and prothrombin G20210A. The LIST study.
Chaireti R; Jennersjö C; Lindahl TL
Thromb Res; 2009 Jun; 124(2):178-84. PubMed ID: 19232683
[TBL] [Abstract][Full Text] [Related]
29. Risk of obstetric and thromboembolic complications in family members of women with previous adverse obstetric outcomes carrying common inherited thombophilias.
Villani M; Tiscia GL; Margaglione M; Colaizzo D; Fischetti L; Vergura P; Grandone E
J Thromb Haemost; 2012 Feb; 10(2):223-8. PubMed ID: 22136658
[TBL] [Abstract][Full Text] [Related]
30. The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or both.
Martinelli I; Bucciarelli P; Margaglione M; De Stefano V; Castaman G; Mannucci PM
Br J Haematol; 2000 Dec; 111(4):1223-9. PubMed ID: 11167765
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Haplotypes of the EPCR gene, prothrombin levels, and the risk of venous thrombosis in carriers of the prothrombin G20210A mutation.
Navarro S; Medina P; Mira Y; Estellés A; Villa P; Ferrando F; Vayá A; Bertina RM; España F
Haematologica; 2008 Jun; 93(6):885-91. PubMed ID: 18403391
[TBL] [Abstract][Full Text] [Related]
33. A FV multiallelic marker detects genetic components of APC resistance contributing to venous thromboembolism in FV Leiden carriers.
Mingozzi F; Legnani C; Lunghi B; Scanavini D; Castoldi E; Palareti G; Marchetti G; Bernardi F
Thromb Haemost; 2003 Jun; 89(6):983-9. PubMed ID: 12783110
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Simultaneous detection of FV Q506 and prothrombin 20210 A variation by allele-specific PCR.
Mitterer M; Lanthaler AJ; Mair W; Giacomuzzi K; Coser P
Haematologica; 1999 Mar; 84(3):204-7. PubMed ID: 10189382
[TBL] [Abstract][Full Text] [Related]
36. Prevalence of 20210 A allele of the prothrombin gene in venous thromboembolism patients.
Leroyer C; Mercier B; Oger E; Chenu E; Abgrall JF; Férec C; Mottier D
Thromb Haemost; 1998 Jul; 80(1):49-51. PubMed ID: 9684784
[TBL] [Abstract][Full Text] [Related]
37. Prothrombotic risk factors in children with spontaneous venous thrombosis and their asymptomatic parents: a family study.
Kosch A; Junker R; Kurnik K; Schobess R; Günther G; Koch H; Nowak-Göttl U
Thromb Res; 2000 Sep; 99(6):531-7. PubMed ID: 10974337
[TBL] [Abstract][Full Text] [Related]
38. Association of a common polymorphism in the factor XIII gene with venous thrombosis.
Catto AJ; Kohler HP; Coore J; Mansfield MW; Stickland MH; Grant PJ
Blood; 1999 Feb; 93(3):906-8. PubMed ID: 9920839
[TBL] [Abstract][Full Text] [Related]
39. 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; 129(2):89-93. PubMed ID: 9669991
[TBL] [Abstract][Full Text] [Related]
40. The A20210 allele in the prothrombin gene enhances the risk of venous thrombosis in carriers of inherited protein S deficiency.
Castaman G; Tosetto A; Cappellari A; Ruggeri M; Rodeghiero F
Blood Coagul Fibrinolysis; 2000 Jun; 11(4):321-6. PubMed ID: 10847418
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]