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Homocysteine and cardiovascular disease : cause or effect?

The American journal of clinical nutrition, 2000-08, Vol.72 (2), p.315-323

2000

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Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease : The result of a meta-analysis

Circulation (New York, N.Y.), 1998-12, Vol.98 (23), p.2520-2526

1998

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The natural history of vascular disease in homocystinuria and the effects of treatment

Journal of inherited metabolic disease, 1997-06, Vol.20 (2), p.295-300

1997

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L-arginine regulates asymmetric dimethylarginine metabolism by inhibiting dimethylarginine dimethylaminohydrolase activity in hepatic (HepG2) cells

Cellular and molecular life sciences : CMLS, 2006-12, Vol.63 (23), p.2838-2846

2006

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Genetic contribution of the endothelial constitutive nitric oxide synthase gene to plasma nitric oxide levels

Arteriosclerosis, thrombosis, and vascular biology, 1997-11, Vol.17 (11), p.3147

1997

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Homocysteine and its disulfide derivatives: a suggested consensus terminology

Arteriosclerosis, thrombosis, and vascular biology, 2000-07, Vol.20 (7), p.1704

2000

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Plasma extracellular superoxide dismutase levels in an Australian population with coronary artery disease

Arteriosclerosis, thrombosis, and vascular biology, 1998-12, Vol.18 (12), p.1915

1998

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Polymorphisms of the apolipoprotein E gene and severity of coronary artery disease defined by angiography

Arteriosclerosis, thrombosis, and vascular biology, 1995-08, Vol.15 (8), p.1030

1995

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Determinants of severity of coronary artery disease in Australian men and women

Circulation (New York, N.Y.), 1994-05, Vol.89 (5), p.1974-1981

1994

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Relationship between homocysteine and superoxide dismutase in homocystinuria: possible relevance to cardiovascular risk

Arteriosclerosis, thrombosis, and vascular biology, 2000-05, Vol.20 (5), p.1199

2000

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Disordered methionine/homocysteine metabolism in premature vascular disease. Its occurrence, cofactor therapy, and enzymology

Arteriosclerosis and thrombosis, 1993-09, Vol.13 (9), p.1253

1993

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NADH/NADPH oxidase p22 phox C242T polymorphism and coronary artery disease in the Australian population

European journal of clinical investigation, 1999-09, Vol.29 (9), p.744-748

1999

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Distribution in healthy and coronary populations of the methylenetetrahydrofolate reductase (MTHFR) C677T mutation

Arteriosclerosis, thrombosis, and vascular biology, 1996-07, Vol.16 (7), p.878

1996

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The Glu-298→Asp (894G→T) mutation at exon 7 of the endothelial nitric oxide synthase gene and coronary artery disease

Journal of molecular medicine (Berlin, Germany), 1999-06, Vol.77 (6), p.511-514

1999

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Elevated circulating homocyst(e)ine levels in placental vascular disease and associated pre‐eclampsia

BJOG : an international journal of obstetrics and gynaecology, 2000-07, Vol.107 (7), p.935-938

2000

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Vascular Complications of Severe Hyperhomocysteinemia in Patients with Homocystinuria Due to Cystathionine β-Synthase Deficiency: Effects of Homocysteine-Lowering Therapy

Seminars in thrombosis and hemostasis, 2000, Vol.26 (3), p.335-340

2000

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Polymorphisms of factor V, factor VII, and fibrinogen genes. Relevance to severity of coronary artery disease

Arteriosclerosis, thrombosis, and vascular biology, 1997-02, Vol.17 (2), p.246

1997

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Strong association between N-acetyltransferase 2 genotype and PD in Hong Kong Chinese

Neurology, 2003-03, Vol.60 (6), p.1002

2003

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Relationship between total plasma homocysteine, polymorphisms of homocysteine metabolism related enzymes, risk factors and coronary artery disease in the Australian hospital-based population

Atherosclerosis, 1999-09, Vol.146 (1), p.133-140

1999

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Overview of inherited metabolic disorders causing cardiovascular disease

Journal of inherited metabolic disease, 2003-01, Vol.26 (2-3), p.245-257

Wilcken, D. E. L.

2003

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Homocysteine, smoking and vascular disease

European heart journal, 2002-10, Vol.23 (20), p.1559-1560

Wilcken, D E L

2002

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Common DNA polymorphisms at the lipoprotein lipase gene : Association with severity of coronary artery disease and diabetes

Circulation (New York, N.Y.), 1996-04, Vol.93 (7), p.1339-1345

1996

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MTHFR 677C→T mutation, folate intake, neural-tube defect, and risk of cardiovascular disease

The Lancet (British edition), 1997-08, Vol.350 (9078), p.603-604

Wilcken, David EL

1997

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Circulating transforming growth factor β1 and coronary artery disease

Cardiovascular research, 1997-05, Vol.34 (2), p.404-410

1997

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Vascular outcome in patients with homocystinuria due to cystathionine beta-synthase deficiency treated chronically: a multicenter observational study

Arteriosclerosis, thrombosis, and vascular biology, 2001-12, Vol.21 (12), p.2080

2001

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Homocysteine and cardiovascular disease : cause or effect?

Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease : The result of a meta-analysis

The natural history of vascular disease in homocystinuria and the effects of treatment

L-arginine regulates asymmetric dimethylarginine metabolism by inhibiting dimethylarginine dimethylaminohydrolase activity in hepatic (HepG2) cells

Genetic contribution of the endothelial constitutive nitric oxide synthase gene to plasma nitric oxide levels

Homocysteine and its disulfide derivatives: a suggested consensus terminology

Plasma extracellular superoxide dismutase levels in an Australian population with coronary artery disease

Polymorphisms of the apolipoprotein E gene and severity of coronary artery disease defined by angiography

Determinants of severity of coronary artery disease in Australian men and women

Relationship between homocysteine and superoxide dismutase in homocystinuria: possible relevance to cardiovascular risk

Disordered methionine/homocysteine metabolism in premature vascular disease. Its occurrence, cofactor therapy, and enzymology

NADH/NADPH oxidase p22 phox C242T polymorphism and coronary artery disease in the Australian population

Distribution in healthy and coronary populations of the methylenetetrahydrofolate reductase (MTHFR) C677T mutation

The Glu-298→Asp (894G→T) mutation at exon 7 of the endothelial nitric oxide synthase gene and coronary artery disease

Elevated circulating homocyst(e)ine levels in placental vascular disease and associated pre‐eclampsia

Vascular Complications of Severe Hyperhomocysteinemia in Patients with Homocystinuria Due to Cystathionine β-Synthase Deficiency: Effects of Homocysteine-Lowering Therapy

Polymorphisms of factor V, factor VII, and fibrinogen genes. Relevance to severity of coronary artery disease

Strong association between N-acetyltransferase 2 genotype and PD in Hong Kong Chinese

Relationship between total plasma homocysteine, polymorphisms of homocysteine metabolism related enzymes, risk factors and coronary artery disease in the Australian hospital-based population

Overview of inherited metabolic disorders causing cardiovascular disease

Homocysteine, smoking and vascular disease

Common DNA polymorphisms at the lipoprotein lipase gene : Association with severity of coronary artery disease and diabetes

MTHFR 677C→T mutation, folate intake, neural-tube defect, and risk of cardiovascular disease

Circulating transforming growth factor β1 and coronary artery disease

Vascular outcome in patients with homocystinuria due to cystathionine beta-synthase deficiency treated chronically: a multicenter observational study

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