601 related articles for article (PubMed ID: 10073951)
1. 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]
2. 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]
3. 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]
4. Prospective evaluation of the thrombotic risk in children with acute lymphoblastic leukemia carrying the MTHFR TT 677 genotype, the prothrombin G20210A variant, and further prothrombotic risk factors.
Nowak-Göttl U; Wermes C; Junker R; Koch HG; Schobess R; Fleischhack G; Schwabe D; Ehrenforth S
Blood; 1999 Mar; 93(5):1595-9. PubMed ID: 10029588
[TBL] [Abstract][Full Text] [Related]
5. Primary thrombophilia in Mexico. II. Factor V G1691A (Leiden), prothrombin G20210A, and methylenetetrahydrofolate reductase C677T polymorphism in thrombophilic Mexican mestizos.
Ruiz-Argüelles GJ; Garcés-Eisele J; Reyes-Núñez V; Ramírez-Cisneros FJ
Am J Hematol; 2001 Jan; 66(1):28-31. PubMed ID: 11426488
[TBL] [Abstract][Full Text] [Related]
6. Factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations are not associated with chronic limb ischemia: the Linz Peripheral Arterial Disease (LIPAD) study.
Mueller T; Marschon R; Dieplinger B; Haidinger D; Gegenhuber A; Poelz W; Webersinke G; Haltmayer M
J Vasc Surg; 2005 May; 41(5):808-15. PubMed ID: 15886665
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Impact of environmental and hereditary risk factors on the clinical manifestation of thrombophilia in homozygous carriers of factor V:G1691A.
Ehrenforth S; Nemes L; Mannhalter C; Rosendaal FR; Koder S; Zoghlami-Rintelen C; Scharrer I; Pabinger I
J Thromb Haemost; 2004 Mar; 2(3):430-6. PubMed ID: 15009459
[TBL] [Abstract][Full Text] [Related]
9. Increased lipoprotein (a) levels as an independent risk factor for venous thromboembolism.
von Depka M; Nowak-Göttl U; Eisert R; Dieterich C; Barthels M; Scharrer I; Ganser A; Ehrenforth S
Blood; 2000 Nov; 96(10):3364-8. PubMed ID: 11071628
[TBL] [Abstract][Full Text] [Related]
10. Venous thromboembolism in young patients from western India: a study.
Ghosh K; Shetty S; Madkaikar M; Pawar A; Nair S; Khare A; Pathare A; Jijina F; Mohanty D
Clin Appl Thromb Hemost; 2001 Apr; 7(2):158-65. PubMed ID: 11292195
[TBL] [Abstract][Full Text] [Related]
11. Risk of venous thromboembolism in carriers of factor V Leiden with a concomitant inherited thrombophilic defect: a retrospective analysis.
Meinardi JR; Middeldorp S; de Kam PJ; Koopman MM; van Pampus EC; Hamulyák K; Prins MH; Büller HR; van der Meer J
Blood Coagul Fibrinolysis; 2001 Dec; 12(8):713-20. PubMed ID: 11734673
[TBL] [Abstract][Full Text] [Related]
12. Methionine synthase A2756G and methylenetetrahydrofolate reductase A1298C polymorphisms are not risk factors for idiopathic venous thromboembolism.
Salomon O; Rosenberg N; Zivelin A; Steinberg DM; Kornbrot N; Dardik R; Inbal A; Seligsohn U
Hematol J; 2001; 2(1):38-41. PubMed ID: 11920232
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Clinical impact of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations among sickle cell disease patients of Central India.
Nishank SS; Singh MP; Yadav R
Eur J Haematol; 2013 Nov; 91(5):462-6. PubMed ID: 23992124
[TBL] [Abstract][Full Text] [Related]
15. Prothrombin and factor V mutations in women with a history of thrombosis during pregnancy and the puerperium.
Gerhardt A; Scharf RE; Beckmann MW; Struve S; Bender HG; Pillny M; Sandmann W; Zotz RB
N Engl J Med; 2000 Feb; 342(6):374-80. PubMed ID: 10666427
[TBL] [Abstract][Full Text] [Related]
16. Frequency of prothrombotic risk factors in patients with deep venous thrombosis and controls: their implications for thrombophilia screening in Chilean subjects.
Guzmán N; Salazar LA
Genet Test Mol Biomarkers; 2010 Oct; 14(5):599-602. PubMed ID: 20707729
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Prevalence of three prothrombotic polymorphisms. Factor V G1691A, factor II G20210A and methylenetetrahydrofolate reductase (MTHFR) C 677T in Argentina. On behalf of the Grupo Cooperativo Argentino de Hemostasia y Trombosis.
Genoud V; Castañon M; Annichino-Bizzacchi J; Korin J; Kordich L
Thromb Res; 2000 Nov; 100(3):127-31. PubMed ID: 11108898
[No Abstract] [Full Text] [Related]
19. Prothrombin G20210A gene mutation and further prothrombotic risk factors in childhood thrombophilia.
Junker R; Koch HG; Auberger K; Münchow N; Ehrenforth S; Nowak-Göttl U
Arterioscler Thromb Vasc Biol; 1999 Oct; 19(10):2568-72. PubMed ID: 10521389
[TBL] [Abstract][Full Text] [Related]
20. Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations.
Grandone E; Margaglione M; Colaizzo D; D'Andrea G; Cappucci G; Brancaccio V; Di Minno G
Am J Obstet Gynecol; 1998 Nov; 179(5):1324-8. PubMed ID: 9822524
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]