Free and protein-bound homocysteine and cysteine in cystathionine β-synthase deficiency: Interrelations during short- and long-term changes in plasma concentrations

Author:

Wiley Veronica C.,Dudman Nicholas P.B.,Wilcken David E.L.

Publisher

Elsevier BV

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference15 articles.

1. Disorders of transsulfuration;Mudd,1983

2. The natural history of homocystinuria due to cystathionine β-synthase deficiency;Mudd;Am J Hum Genet,1985

3. Heterozygosity for homocystinuria in premature peripheral and cerebral occlusive arterial disease;Boers;N Engl J Med,1985

4. Homocysteinemia, ischemic heart disease, and the carrier state for homocystinuria;Wilcken;Metabolism,1983

5. Moderate homocysteinemia—a possible risk factor for cerebrovascular disease;Brattstrom;Stroke,1984

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3. Hypermethioninemias of genetic and non-genetic origin: A review;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2011-02-09

4. Molecular Targeting of Proteins by L-Homocysteine: Mechanistic Implications for Vascular Disease;Antioxidants & Redox Signaling;2007-11

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