| Unbound MEDLINE results for: | Bookmark this site | | Articles related to 11011848 [Unique ID], provided by the PubMed system | |
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| | 1 - 10 of 440 journal articles in the PubMed database | Email to a friend | | |
| De Stefano V, Casorelli I, Rossi E, et al.
Interaction between hyperhomocysteinemia and inherited thrombophilic factors in venous thromboembolism. [Journal Article, Review]
Semin Thromb Hemost 2000; 26(3):305-11.
Abstract | Full Citation | Find Related Articles | | Morelli VM, Lourenço DM, D'Almeida V, et al.
Hyperhomocysteinemia increases the risk of venous thrombosis independent of the C677T mutation of the methylenetetrahydrofolate reductase gene in selected Brazilian patients. [Journal Article]
Blood Coagul Fibrinolysis 2002 Apr; 13(3):271-5.
Abstract | Full Citation | Find Related Articles | | Domagala TB, Adamek L, Nizankowska E, et al.
Mutations C677T and A1298C of the 5,10-methylenetetrahydrofolate reductase gene and fasting plasma homocysteine levels are not associated with the increased risk of venous thromboembolic disease. [Journal Article]
Blood Coagul Fibrinolysis 2002 Jul; 13(5):423-31.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Keijzer MB, den Heijer M, Blom HJ, et al.
Interaction between hyperhomocysteinemia, mutated methylenetetrahydrofolatereductase (MTHFR) and inherited thrombophilic factors in recurrent venous thrombosis. [Journal Article]
Thromb Haemost 2002 Nov; 88(5):723-8.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Ruiz-Argüelles GJ, Garcés-Eisele J, Reyes-Núñez V, et al.
Primary thrombophilia in Mexico. II. Factor V G1691A (Leiden), prothrombin G20210A, and methylenetetrahydrofolate reductase C677T polymorphism in thrombophilic Mexican mestizos. [Journal Article]
Am J Hematol 2001 Jan; 66(1):28-31.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Cattaneo M, Chantarangkul V, Taioli E, et al.
The G20210A mutation of the prothrombin gene in patients with previous first episodes of deep-vein thrombosis: prevalence and association with factor V G1691A, methylenetetrahydrofolate reductase C677T and plasma prothrombin levels. [Journal Article]
Thromb Res 1999 Jan 1; 93(1):1-8.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Almawi WY, Tamim H, Kreidy R, et al.
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. [Journal Article]
J Thromb Thrombolysis 2005 Jun; 19(3):189-96.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Gemmati D, Serino ML, Trivellato C, et al.
C677T substitution in the methylenetetrahydrofolate reductase gene as a risk factor for venous thrombosis and arterial disease in selected patients. [Journal Article]
Haematologica 1999 Sep; 84(9):824-8.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Martinelli I, De Stefano V, Taioli E, et al.
Inherited thrombophilia and first venous thromboembolism during pregnancy and puerperium. [Journal Article, Multicenter Study]
Thromb Haemost 2002 May; 87(5):791-5.
Abstract | Full Citation | Find Related Articles |   |
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