Hyperhomocysteinemia and the Endocrine System: Implications for Atherosclerosis and Thrombosis

Author:

Fonseca Vivian1,Guba Susan C.2,Fink Louis M.2

Affiliation:

1. Department of Medicine, Section of Endocrinology, Tulane University Medical School (V.F.), New Orleans, Louisiana 70112;

2. The Department of Pathology, University of Arkansas for Medical Sciences and the John L. McClellan Memorial Veterans Hospital (S.C.G., L.M.F.), Little Rock, Arkansas

Publisher

The Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference204 articles.

1. Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease.;Kluijtmans;Am J Hum Genet,1996

2. Nutritional ecogenetics: homocysteine-related arteriosclerotic vascular disease, neural tube defects, and folic acid.;Motulsky;Am J Hum Genet,1996

3. Homocysteine and ischemic heart disease: results of a prospective study with implications regarding prevention.;Wald;Arch Int Med,1998

4. Homocysteine and coronary artery disease in French Canadian subjects: relation with vitamins B12, B6, pyridoxal phosphate, and folate.;Dalery;Am J Cardiol,1995

5. Association between plasma homocysteine concentrations and extracranial carotid-artery stenosis.;Selhub;N Engl J Med,1995

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