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Homocystinuria: A risk factor of premature vascular disease

Boers, G. H. J

1, 2019

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Homocysteine and folate status in methotrexate‐treated patients with rheumatoid arthritis

Rheumatology (Oxford, England), 2002-06, Vol.41 (6), p.658-665

2002

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Unfiltered coffee increases plasma homocysteine concentrations in healthy volunteers: a randomized trial

The American journal of clinical nutrition, 2000-02, Vol.71 (2), p.480-484

2000

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Plasma homocysteine and menopausal status

European journal of clinical investigation, 1995-11, Vol.25 (11), p.801-805

1995

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Hyperhomocysteinaemia and endothelial dysfunction in young patients with peripheral arterial occlusive disease

European journal of clinical investigation, 1995-03, Vol.25 (3), p.176-181

1995

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Delay in diagnosis of homocystinuria: retrospective study of consecutive patients

BMJ (Online), 1996-10, Vol.313 (7064), p.1037

International edition, 1996

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Lipid peroxidation and susceptibility of low-density lipoprotein to in vitro oxidation in hyperhomocysteinaemia

European journal of clinical investigation, 1995-03, Vol.25 (3), p.149-154

1995

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Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease

American journal of human genetics, 1996-01, Vol.58 (1), p.35-41

1996

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Neural tube defects and elevated homocysteine levels in amniotic fluid

American journal of obstetrics and gynecology, 1995-05, Vol.172 (5), p.1436-1441

1995

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Hyperhomocysteinemia as a risk factor for arterial and venous disease. A review of evidence and relevance

Thrombosis and haemostasis, 1997-07, Vol.78 (1), p.520

Boers, G H

1997

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Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia

American journal of human genetics, 1995, Vol.56 (1), p.142-150

1995

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Three Different Methods for the Determination of Total Homocysteine in Plasma

Annals of clinical biochemistry, 1995-03, Vol.32 (2), p.218-220

1995

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Thermolabile methylenetetrahydrofolate reductase in coronary artery disease

Circulation (New York, N.Y.), 1997-10, Vol.96 (8), p.2573-2577

1997

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Maternal hyperhomocysteinemia: A risk factor for neural-tube defects?

Metabolism, clinical and experimental, 1994-12, Vol.43 (12), p.1475-1480

1994

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Methylenetetrahydrofolate reductase polymorphism affects the change in homocysteine and folate concentrations resulting from low dose folic acid supplementation in women with unexplained recurrent miscarriages

The Journal of nutrition, 1998-08, Vol.128 (8), p.1336-1341

1998

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Carotid and femoral artery wall thickness and stiffness in patients at risk for cardiovascular disease, with special emphasis on hyperhomocysteinemia

Arteriosclerosis, thrombosis, and vascular biology, 1998-12, Vol.18 (12), p.1958

1998

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Hyperhomocysteinemia: a risk factor in women with unexplained recurrent early pregnancy loss

Fertility and sterility, 1993-11, Vol.60 (5), p.820-825

1993

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Homocysteine metabolism in endothelial cells of a patient homozygous for cystathionine beta-synthase (CS) deficiency

Thrombosis and haemostasis, 1997-08, Vol.78 (2), p.827

1997

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Homocystinuria: what about mild hyperhomocysteinaemia?

Postgraduate Medical Journal, 1996-09, Vol.72 (851), p.513-518

1996

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The case for mild hyperhomocysteinaemia as a risk factor

Journal of inherited metabolic disease, 1997-06, Vol.20 (2), p.301-306

Boers, G. H. J.

1997

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Effect of various regimens of vitamin B6 and folic acid on mild hyperhomocysteinaemia in vascular patients

Journal of inherited metabolic disease, 1994-01, Vol.17 (1), p.159-162

1994

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Hyperhomocysteinemia: a risk factor for placental abruption or infarction

European journal of obstetrics & gynecology and reproductive biology, 1996-05, Vol.66 (1), p.23-29

1996

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Hyperhomocysteinaemia; with reference to its neuroradiological aspects

Neuroradiology, 1995-07, Vol.37 (5), p.403-411

1995

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The Molecular Basis of Cystathionine β-Synthase Deficiency in Dutch Patients with Homocystinuria: Effect of CBS Genotype on Biochemical and Clinical Phenotype and on Response to Treatment

American journal of human genetics, 1999-07, Vol.65 (1), p.59-67

1999

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Methionine transamination in patients with homocystinuria due to cystathionine β-synthase deficiency

Metabolism, clinical and experimental, 2000-08, Vol.49 (8), p.1071-1077

2000

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Homocystinuria: A risk factor of premature vascular disease

Homocysteine and folate status in methotrexate‐treated patients with rheumatoid arthritis

Unfiltered coffee increases plasma homocysteine concentrations in healthy volunteers: a randomized trial

Plasma homocysteine and menopausal status

Hyperhomocysteinaemia and endothelial dysfunction in young patients with peripheral arterial occlusive disease

Delay in diagnosis of homocystinuria: retrospective study of consecutive patients

Lipid peroxidation and susceptibility of low-density lipoprotein to in vitro oxidation in hyperhomocysteinaemia

Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease

Neural tube defects and elevated homocysteine levels in amniotic fluid

Hyperhomocysteinemia as a risk factor for arterial and venous disease. A review of evidence and relevance

Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia

Three Different Methods for the Determination of Total Homocysteine in Plasma

Thermolabile methylenetetrahydrofolate reductase in coronary artery disease

Maternal hyperhomocysteinemia: A risk factor for neural-tube defects?

Methylenetetrahydrofolate reductase polymorphism affects the change in homocysteine and folate concentrations resulting from low dose folic acid supplementation in women with unexplained recurrent miscarriages

Carotid and femoral artery wall thickness and stiffness in patients at risk for cardiovascular disease, with special emphasis on hyperhomocysteinemia

Hyperhomocysteinemia: a risk factor in women with unexplained recurrent early pregnancy loss

Homocysteine metabolism in endothelial cells of a patient homozygous for cystathionine beta-synthase (CS) deficiency

Homocystinuria: what about mild hyperhomocysteinaemia?

The case for mild hyperhomocysteinaemia as a risk factor

Effect of various regimens of vitamin B6 and folic acid on mild hyperhomocysteinaemia in vascular patients

Hyperhomocysteinemia: a risk factor for placental abruption or infarction

Hyperhomocysteinaemia; with reference to its neuroradiological aspects

The Molecular Basis of Cystathionine β-Synthase Deficiency in Dutch Patients with Homocystinuria: Effect of CBS Genotype on Biochemical and Clinical Phenotype and on Response to Treatment

Methionine transamination in patients with homocystinuria due to cystathionine β-synthase deficiency

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