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Journal Abstract Search

474 related items for PubMed ID: 12095808

  • 21. Effect of MTHFR 677C>T on plasma total homocysteine levels in renal graft recipients.
    Födinger M, Wölfl G, Fischer G, Rasoul-Rockenschaub S, Schmid R, Hörl WH, Sunder-Plassmann G.
    Kidney Int; 1999 Mar; 55(3):1072-80. PubMed ID: 10027946
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  • 23. C677T substitution in the methylenetetrahydrofolate reductase gene as a risk factor for venous thrombosis and arterial disease in selected patients.
    Gemmati D, Serino ML, Trivellato C, Fiorini S, Scapoli GL.
    Haematologica; 1999 Sep; 84(9):824-8. PubMed ID: 10477457
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  • 24. Thermolabile MTHFR genotype and retinal vascular occlusive disease.
    Cahill M, Karabatzaki M, Donoghue C, Meleady R, Mynett-Johnson LA, Mooney D, Graham IM, Whitehead AS, Shields DC.
    Br J Ophthalmol; 2001 Jan; 85(1):88-90. PubMed ID: 11133719
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  • 26. The C677T mutation in the methylenetetrahydrofolate reductase gene contributes to hyperhomocysteinemia in patients taking anticonvulsants.
    Ono H, Sakamoto A, Mizoguchi N, Sakura N.
    Brain Dev; 2002 Jun; 24(4):223-6. PubMed ID: 12015164
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  • 27. The 677C-->T mutation in the methylenetetrahydrofolate reductase gene: associations with plasma total homocysteine levels and risk of coronary atherosclerotic disease.
    Verhoef P, Kok FJ, Kluijtmans LA, Blom HJ, Refsum H, Ueland PM, Kruyssen DA.
    Atherosclerosis; 1997 Jul 11; 132(1):105-13. PubMed ID: 9247365
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  • 28. The relation between erythrocyte volume and folate levels is influenced by a common mutation in the methylenetetrahydrofolate reductase (MTHFR) gene (C677T).
    Lalouschek W, Aull S, Serles W, Wolfsberger M, Deecke L, Pabinger-Fasching I, Mannhalter C.
    J Investig Med; 2000 Jan 11; 48(1):14-20. PubMed ID: 10695265
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  • 29. Hyperhomocysteinemia and retinal vascular occlusive disease.
    Abu El-Asrar AM, Abdel Gader AG, Al-Amro SA, Al-Attas OS.
    Eur J Ophthalmol; 2002 Jan 11; 12(6):495-500. PubMed ID: 12510718
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  • 32. Thrombophilia as a cause for central and branch retinal artery occlusion in patients without an apparent embolic source.
    Salomon O, Huna-Baron R, Moisseiev J, Rosenberg N, Rubovitz A, Steinberg DM, Davidson J, Sela BA, Seligsohn U.
    Eye (Lond); 2001 Aug 11; 15(Pt 4):511-4. PubMed ID: 11767028
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  • 33. 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 11; 13(3):271-5. PubMed ID: 11943942
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  • 34. Opposite effects of plasma homocysteine and the methylenetetrahydrofolate reductase C677T mutation on carotid artery geometry in asymptomatic adults.
    Demuth K, Moatti N, Hanon O, Benoit MO, Safar M, Girerd X.
    Arterioscler Thromb Vasc Biol; 1998 Dec 11; 18(12):1838-43. PubMed ID: 9848874
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  • 36. 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 11; 20(11):2448-52. PubMed ID: 11073851
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  • 39. Interplay between methylenetetrahydrofolate reductase gene polymorphism 677C-->T and serum folate levels in determining hyperhomocysteinemia in heart transplant recipients.
    Potena L, Grigioni F, Viggiani M, Magnani G, Sorbello S, Falchetti E, Sassi S, Mantovani V, Bacchi-Reggiani L, Magelli C, Branzi A.
    J Heart Lung Transplant; 2001 Dec 11; 20(12):1245-51. PubMed ID: 11744407
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  • 40. Homocysteine, methylenetetrahydrofolate reductase C677T polymorphism and the B-vitamins: a facet of nature-nurture interplay.
    Herrmann W, Obeid R, Schorr H, Zarzour W, Geisel J.
    Clin Chem Lab Med; 2003 Apr 11; 41(4):547-53. PubMed ID: 12747601
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