(Q51560773)

7 April 2018

title

Serum homocysteine, MTHFR gene polymorphism, and carotid intimal-medial thickness in NIDDM subjects. (English)

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author

Anna Pastore

4

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author name string

A Mazza

1

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C Motti

2

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A Nulli

3

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F Andreotti

5

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V Ammaturo

6

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P Bianco

7

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E Santoro

8

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G Federici

9

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C Cortese

10

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publication date

1 October 1999

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Journal of Thrombosis and Thrombolysis

published in

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volume

8

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issue

3

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page(s)

207-212

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https://scigraph.springernature.com/pub.10.1023/a:1008962220476

exact match

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cites work

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1 reference

12 December 2020

Association of methylenetetrahydrofolate reductase gene polymorphism with carotid arterial wall thickening and myocardial infarction risk in NIDDM

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12 December 2020

Carotid artery intimal-medial wall thickening and plasma homocyst(e)ine in asymptomatic adults. The Atherosclerosis Risk in Communities Study

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12 December 2020

A Quantitative Assessment of Plasma Homocysteine as a Risk Factor for Vascular Disease

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12 December 2020

Plasma total homocysteine and cysteine in relation to glomerular filtration rate in diabetes mellitus

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12 December 2020

Increased levels of plasma homocysteine are associated with nephropathy, but not severe retinopathy in type 1 diabetes mellitus

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12 December 2020

Homocysteine and risk of premature coronary heart disease. Evidence for a common gene mutation

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12 December 2020

Plasma homocysteine concentrations in patients with type 1 diabetes.

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12 December 2020

Intimal plus medial thickness of the arterial wall: a direct measurement with ultrasound imaging

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Common mutation in methylenetetrahydrofolate reductase. Correlation with homocysteine and other risk factors for vascular disease.

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12 December 2020

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

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12 December 2020

Methylenetetrahydrofolate reductase (MTHFR) mutation, homocyst(e)ine, and coronary artery disease

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12 December 2020

The cellular and molecular mechanisms of diabetic complications

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Nutritional ecogenetics: homocysteine-related arteriosclerotic vascular disease, neural tube defects, and folic acid

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Elevated total plasma homocysteine and 677C-->T mutation of the 5,10-methylenetetrahydrofolate reductase gene in thrombotic vascular disease

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Hyperhomocyst(e)inemia and endothelial dysfunction in IDDM.

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12 December 2020

Carotid intima-media thickness and coronary heart disease risk factors

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12 December 2020

Defective homocysteine metabolism as a risk factor for diabetic retinopathy

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Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery disease.

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Hyperhomocysteinemia following a methionine load in patients with non-insulin-dependent diabetes mellitus and macrovascular disease

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Divergent association of apolipoprotein E polymorphism with vascular disease in patients with NIDDM and control subjects

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12 December 2020

Fully automated assay for total homocysteine, cysteine, cysteinylglycine, glutathione, cysteamine, and 2-mercaptopropionylglycine in plasma and urine.

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Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification

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

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12 December 2020

Hyperhomocysteinemia: an independent risk factor for vascular disease

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Plasma homocysteine concentrations in Japanese patients with non-insulin-dependent diabetes mellitus: effect of parenteral methylcobalamin treatment

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12 December 2020

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

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Moderate hyperhomocysteinaemia and retinopathy in insulin-dependent diabetes

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12 December 2020

Type 1 diabetes mellitus and homocyst(e)ine

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12 December 2020

Hyperhomocysteinemia is associated with an increased risk of cardiovascular disease, especially in non-insulin-dependent diabetes mellitus: a population-based study

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12 December 2020

Oxidative stress and diabetic vascular complications

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12 December 2020

Homocysteine and vascular disease

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12 December 2020

The (Ala-Val) mutation of methylenetetrahydrofolate reductase as a genetic risk factor for vascular disease in non-insulin-dependent diabetic patients

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Identifiers

DOI

10.1023/A:1008962220476

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7 April 2018

Dimensions Publication ID

1042855060

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7 April 2018