Homocysteine and the MTHFR 677C→T allele in premature coronary artery disease. Case control and family studies-Reference-Cited by-同舟云学术

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Homocysteine and the MTHFR 677C→T allele in premature coronary artery disease. Case control and family studies

Published:2001-01 Issue:1 Volume:31 Page:24-30
ISSN:0014-2972
Container-title:European Journal of Clinical Investigation
language:en
Short-container-title:

Author:

Pintó X.,Vilaseca M. A.,Garcia-Giralt N.,Ferrer I.,Palá M.,Meco J. F.,Mainou C.,Ordovás J. M.,Grinberg D.,Balcells S.,

Publisher

Wiley

Subject

Clinical Biochemistry,Biochemistry,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2362.2001.00760.x/fullpdf

Reference33 articles.

1. Plasma homocyst(e)ine levels in men with premature coronary artery disease;Genest;J Am Coll Cardiol,1990

2. A prospective study of plasma homocyst(e)ine and risk of myocardial infarction in US physicians;Stampfer;JAMA,1992

3. A quantitative assessment of plasma homocysteine as a risk factor for vascular disease. Probable benefits of increasing folic acid intakes;Boushey;JAMA,1995

4. Total plasma homocysteine and cardiovascular risk profile. The Hordaland Homocysteine Study;Nygard;JAMA,1995

5. Plasma homocysteine as a risk factor for vascular disease: The European concerted action project;Graham;JAMA,1997

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2. Risk factors of premature coronary artery disease in Iran: A systematic review and meta‐analysis;European Journal of Clinical Investigation;2019-05-18

3. Genetic polymorphism of MTHFR C677T and premature coronary artery disease susceptibility: A meta-analysis;Gene;2015-07

4. Possible influence of MTHFR C677T polymorphism on serum lipid levels in Serbian school children;Archives of Biological Sciences;2014

5. Methylenetetrahydrofolate reductase C677T polymorphism in patients with Henoch-Schönlein purpura;Pediatrics International;2011-06

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