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Journal Abstract Search

280 related items for PubMed ID: 10650848

  • 1. The 677T genotype of the common MTHFR thermolabile variant and fasting homocysteine in childhood venous thrombosis.
    Koch HG, Nabel P, Junker R, Auberger K, Schobess R, Homberger A, Linnebank M, Nowak-Göttl U.
    Eur J Pediatr; 1999 Dec; 158 Suppl 3():S113-6. PubMed ID: 10650848
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  • 2. 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.
    Domagala TB, Adamek L, Nizankowska E, Sanak M, Szczeklik A.
    Blood Coagul Fibrinolysis; 2002 Jul; 13(5):423-31. PubMed ID: 12138370
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  • 3. Role of genetic prothrombotic risk factors in childhood caval vein thrombosis.
    Münchow N, Kosch A, Schobess R, Junker R, Auberger K, Nowak-Göttl U.
    Eur J Pediatr; 1999 Dec; 158 Suppl 3():S109-12. PubMed ID: 10650847
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  • 5. Prevalence of methylenetetrahydrofolate reductase C677T and its association with arterial and venous thrombosis in the Chinese population.
    Zheng YZ, Tong J, Do XP, Pu XQ, Zhou BT.
    Br J Haematol; 2000 Jun; 109(4):870-4. PubMed ID: 10929044
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  • 6. 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.
    Cattaneo M, Chantarangkul V, Taioli E, Santos JH, Tagliabue L.
    Thromb Res; 1999 Jan 01; 93(1):1-8. PubMed ID: 10065893
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  • 8. Hyperhomocysteinemia and other inherited prothrombotic conditions in young adults with a history of ischemic stroke.
    Madonna P, de Stefano V, Coppola A, Cirillo F, Cerbone AM, Orefice G, Di Minno G.
    Stroke; 2002 Jan 01; 33(1):51-6. PubMed ID: 11779888
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  • 9. Association study of methylenetetrahydrofolate reductase C677T mutation with cerebral venous thrombosis in an Iranian population.
    Ghaznavi H, Soheili Z, Samiei S, Soltanpour MS.
    Blood Coagul Fibrinolysis; 2015 Dec 01; 26(8):869-73. PubMed ID: 26083986
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  • 10. The role of vitamin B12 in fasting hyperhomocysteinemia and its interaction with the homozygous C677T mutation of the methylenetetrahydrofolate reductase (MTHFR) gene. A case-control study of patients with early-onset thrombotic events.
    D'Angelo A, Coppola A, Madonna P, Fermo I, Pagano A, Mazzola G, Galli L, Cerbone AM.
    Thromb Haemost; 2000 Apr 01; 83(4):563-70. PubMed ID: 10780318
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  • 11. Methylenetetrahydrofolate reductase 677 C-->T mutation and coronary heart disease risk in UK Indian Asians.
    Chambers JC, Ireland H, Thompson E, Reilly P, Obeid OA, Refsum H, Ueland P, Lane DA, Kooner JS.
    Arterioscler Thromb Vasc Biol; 2000 Nov 01; 20(11):2448-52. PubMed ID: 11073851
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  • 12. C677T and A1298C polymorphisms of the methylenetetrahydrofolate reductase gene: incidence and effect of combined genotypes on plasma fasting and post-methionine load homocysteine in vascular disease.
    Hanson NQ, Aras O, Yang F, Tsai MY.
    Clin Chem; 2001 Apr 01; 47(4):661-6. PubMed ID: 11274015
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  • 13. Interaction between hyperhomocysteinemia, mutated methylenetetrahydrofolatereductase (MTHFR) and inherited thrombophilic factors in recurrent venous thrombosis.
    Keijzer MB, den Heijer M, Blom HJ, Bos GM, Willems HP, Gerrits WB, Rosendaal FR.
    Thromb Haemost; 2002 Nov 01; 88(5):723-8. PubMed ID: 12428084
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  • 14. Hyperhomocysteinemia and the MTHFR C677T mutation in Budd-Chiari syndrome.
    Li XM, Wei YF, Hao HL, Hao YB, He LS, Li JD, Mei B, Wang SY, Wang C, Wang JX, Zhu JZ, Liang JQ.
    Am J Hematol; 2002 Sep 01; 71(1):11-4. PubMed ID: 12221667
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  • 15. Factor V G1691A, prothrombin G20210A, and methylenetetrahydrofolate reductase [MTHFR] C677T gene polymorphism in angiographically documented coronary artery disease.
    Almawi WY, Ameen G, Tamim H, Finan RR, Irani-Hakime N.
    J Thromb Thrombolysis; 2004 Jun 01; 17(3):199-205. PubMed ID: 15353918
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  • 16. Hyperhomocysteinemia increases the risk of venous thrombosis independent of the C677T mutation of the methylenetetrahydrofolate reductase gene in selected Brazilian patients.
    Morelli VM, Lourenço DM, D'Almeida V, Franco RF, Miranda F, Zago MA, Noguti MA, Cruz E, Kerbauy J.
    Blood Coagul Fibrinolysis; 2002 Apr 01; 13(3):271-5. PubMed ID: 11943942
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  • 17. Polymorphism in methylenetetrahydrofolate reductase gene: its impact on plasma homocysteine levels and carotid atherosclerosis in ESRD patients receiving hemodialysis.
    Lim PS, Hung WR, Wei YH.
    Nephron; 2001 Mar 01; 87(3):249-56. PubMed ID: 11287760
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