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D'Angelo A, Coppola A, Madonna P, et al. 
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. [Journal Article]
Thromb Haemost 2000 Apr; 83(4):563-70.
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Postiglione A, Milan G, Ruocco A, et al. 
Plasma folate, vitamin B(12), and total homocysteine and homozygosity for the C677T mutation of the 5,10-methylene tetrahydrofolate reductase gene in patients with Alzheimer's dementia. A case-control study. [Journal Article]
Gerontology 2001 Nov-Dec; 47(6):324-9.
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Födinger M, Mannhalter C, Wölfl G, et al. 
Mutation (677 C to T) in the methylenetetrahydrofolate reductase gene aggravates hyperhomocysteinemia in hemodialysis patients. [Journal Article]
Kidney Int 1997 Aug; 52(2):517-23.
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de Jong SC, Stehouwer CD, van den Berg M, et al. 
Determinants of fasting and post-methionine homocysteine levels in families predisposed to hyperhomocysteinemia and premature vascular disease. [Journal Article]
Arterioscler Thromb Vasc Biol 1999 May; 19(5):1316-24.
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Billion S, Tribout B, Cadet E, et al. 
Hyperhomocysteinaemia, folate and vitamin B12 in unsupplemented haemodialysis patients: effect of oral therapy with folic acid and vitamin B12. [Journal Article]
Nephrol Dial Transplant 2002 Mar; 17(3):455-61.
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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.
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de Franchis R, Fermo I, Mazzola G, et al. 
Contribution of the cystathionine beta-synthase gene (844ins68) polymorphism to the risk of early-onset venous and arterial occlusive disease and of fasting hyperhomocysteinemia. [Journal Article]
Thromb Haemost 2000 Oct; 84(4):576-82.
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Anwar W, Guéant JL, Abdelmouttaleb I, et al. 
Hyperhomocysteinemia is related to residual glomerular filtration and folate, but not to methylenetetrahydrofolate-reductase and methionine synthase polymorphisms, in supplemented end-stage renal disease patients undergoing hemodialysis. [Journal Article]
Clin Chem Lab Med 2001 Aug; 39(8):747-52.
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McQuillan BM, Beilby JP, Nidorf M, et al. 
Hyperhomocysteinemia but not the C677T mutation of methylenetetrahydrofolate reductase is an independent risk determinant of carotid wall thickening. The Perth Carotid Ultrasound Disease Assessment Study (CUDAS) [Journal Article]
Circulation 1999 May 11; 99(18):2383-8.
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