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The natural history of vascular disease in homocystinuria and the effects of treatment

  • Published:1997-06 Issue:2 Volume:20 Page:295-300
  • ISSN:0141-8955
  • Container-title:Journal of Inherited Metabolic Disease
  • language:en
  • Short-container-title:J Inherit Metab Dis

Author:

Wilcken D. E. L.12,Wilcken B.3

Affiliation:

1. ; Department of Cardiovascular Medicine; University of New South Wales, The Prince Henry and Prince of Wales Hospitals; Sydney

2. ; Department of Cardiovascular Medicine, Clinical Sciences Building; The Prince Henry Hospital; Little Bay Sydney 2036 Australia

3. ; The New Children's Hospital; Westmead, Sydney Australia

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference15 articles.

1. Vitamin B6 safety issues;Bendich;Ann NY Acad Sci,1990

2. Impaired endothelial function occurs in the systemic arteries of children with homozygous homocystinuria but not in their heterozygous parents;Celemajer;J Am Coll Cardiol,1993

3. Coexistence of hereditary homocystinuria and factor V Leiden - effect on thrombosis;Mandel;New Engl J Med,1996

4. Homocysteine and coronary atherosclerosis;Mayer;J Am Coll Cardiol,1996

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

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1. Hyperhomocysteinemia in Adult Patients: A Treatable Metabolic Condition;Nutrients;2023-12-30

2. Cystathionine beta-Synthase in hypoxia and ischemia/reperfusion: A current overview;Archives of Biochemistry and Biophysics;2022-03

3. Hyperhomocysteinemia and cardiovascular diseases;Annales de Biologie Clinique;2022-02

4. Homocystinuria and Cobalamin Disorders;Nutrition Management of Inherited Metabolic Diseases;2022

5. Role of Homocysteine Metabolism in Cardiovascular Diseases;Homocysteine Metabolism in Health and Disease;2022
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