(Q51564037)

7 April 2018

title

Genetic causes of mild hyperhomocysteinemia in patients with premature occlusive coronary artery diseases. (English)

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7 April 2018

author

Michael Y. Tsai

1

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7 April 2018

author name string

Welge BG

2

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7 April 2018

Hanson NQ

3

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7 April 2018

Bignell MK

4

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7 April 2018

Vessey J

5

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Schwichtenberg K

6

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7 April 2018

Yang F

7

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Bullemer FE

8

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Rasmussen R

9

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Graham KJ

10

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publication date

1 March 1999

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7 April 2018

published in

Atherosclerosis

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7 April 2018

volume

143

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7 April 2018

issue

1

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7 April 2018

page(s)

163-170

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7 April 2018

Association between Plasma Homocysteine Concentrations and Extracranial Carotid-Artery Stenosis

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900271-8

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7 January 2021

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Serum total homocysteine and coronary heart disease

7 January 2021

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Prospective study of serum total homocysteine concentration and risk of stroke in middle-aged British men.

7 January 2021

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Plasma homocysteine levels and mortality in patients with coronary artery disease

7 January 2021

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Heterozygosity for Homocystinuria in Premature Peripheral and Cerebral Occlusive Arterial Disease

7 January 2021

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Hyperhomocysteinemia: an independent risk factor for vascular disease

7 January 2021

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Molecular and biochemical approaches in the identification of heterozygotes for homocystinuria

7 January 2021

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Excess prevalence of fasting and postmethionine-loading hyperhomocysteinemia in stable renal transplant recipients

7 January 2021

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Hyperhomocysteinemia in premature arterial disease: examination of cystathionine beta-synthase alleles at the molecular level.

7 January 2021

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

7 January 2021

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Methylenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine, and risk of myocardial infarction in US physicians

7 January 2021

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Methylenetetrahydrofolate reductase gene and coronary artery disease

7 January 2021

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A common mutation in methylenetetrahydrofolate reductase gene is not a major risk of coronary artery disease or myocardial infarction

7 January 2021

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Correlation of a common mutation in the methylenetetrahydrofolate reductase gene with plasma homocysteine in patients with premature coronary artery disease.

7 January 2021

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The 677C-->T mutation in the methylenetetrahydrofolate reductase gene: associations with plasma total homocysteine levels and risk of coronary atherosclerotic disease.

7 January 2021

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Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders

7 January 2021

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Cloning, mapping and RNA analysis of the human methionine synthase gene

7 January 2021

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Defects in human methionine synthase in cblG patients

7 January 2021

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High frequency (71%) of cystathionine β-synthase mutation G307S in Irish homocystinuria patients

7 January 2021

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Molecular basis of cystathionine beta-synthase deficiency in pyridoxine responsive and nonresponsive homocystinuria

7 January 2021

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Prospective study of coronary heart disease incidence in relation to fasting total homocysteine, related genetic polymorphisms, and B vitamins: the Atherosclerosis Risk in Communities (ARIC) study.

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900271-8

Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations.

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900271-8

Estimates of heritability of plasma homocyst(e)ine levels in aging adult male twins

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900271-8

10.1016/S0021-9150(98)00271-8

7 January 2021

Identifiers

DOI

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7 April 2018

release_76dylcn3ifcf5d7hxfk42kv2le

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/76dylcn3ifcf5d7hxfk42kv2le

mapped directly with Wikidata item

24 November 2022

based on heuristic

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7 April 2018