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Volumn 97, Issue 6, 1997, Pages 215-217

Approaches to defining the optimal dietary folate intake for cardiovascular health

Author keywords

Diet; Diseases; Health; Nutrition

Indexed keywords


EID: 84986047412     PISSN: 00346659     EISSN: None     Source Type: Journal    
DOI: 10.1108/00346659710180316     Document Type: Article
Times cited : (1)

References (13)
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    • supplement 1
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    • Celermajer, D.S., Sorensen, K., Ryalls, M., Robinson, J., Thomas, O., Leonard, J.V. and Deanfield, J.E. (1993), “Impaired endothelial function occurs in systemic arteries of children with homozygous homocystinuria but not in their heterozygous parents”, Journal American College of Cardiology, Vol. 22, pp. 854-8.
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  • 5
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    • Frosst, P., Blom, H.J., Milos, P., Goyette, P., Shepperd, C.A. and Matthews, R.G. (1995), “A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase”, Nature Genetics, Vol. 10, pp. 111-3.
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  • 6
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    • Endothelium and inelastic arteries: an early marker of vascular dysfucntion in non-insulin dependent diabetes
    • Goodfellow, J., Ramsey, M.W., Luddington, L.A., Jones, C.J.H., Coates, P.A. and Dunstan, F. (1996), “Endothelium and inelastic arteries: an early marker of vascular dysfucntion in non-insulin dependent diabetes”, British Medical Journal, Vol. 312, pp. 744-5.
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    • The common ‘thermolabile’ variant of methylene tetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia
    • Harmon, D.L., Woodside, J.V., Yarnell, J.W.G., McMaster, D., Young, I.S. and McCrum, E.E. (1996), “The common ‘thermolabile’ variant of methylene tetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia”, Quarterly Journal of Medicine, Vol. 89, pp. 571-7.
    • (1996) Quarterly Journal of Medicine , vol.89 , pp. 571-577
    • Harmon, D.L.1    Woodside, J.V.2    Yarnell, J.W.G.3    McMaster, D.4    Young, I.S.5    McCrum, E.E.6
  • 9
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.