Hyperhomocyst(e)inemia. A common and easily reversible risk factor for occlusive atherosclerosis.

Author:

Malinow M R1

Affiliation:

1. Oregon Regional Primate Research Center, Beaverton 97006.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference33 articles.

1. Mudd SH Levy HL: Disorders of transsulfuration in Stanbury JB Wingarden JB Fredrickson DS Goldstein JL Brown MS (eds): The Metabolic Basis of Inherited Disease. New York McGraw-Hill 1983 pp 522-559

2. Brattstrom L: Homocysteine in Vascular Disease: A Clinical Study of Homocysteine Metabolism in Health and in Vascular Disease. Lund 1989

3. Homocystinuria associated with decreased methylenetetrahydrofolate reductase activity

4. Erbe RW: Inborn error of folate metabolism in Blakeley RL Whitehead VM (eds): Folate and Pterine Volume 3. New York John Wiley and Sons 1986 pp 413-465

5. Inherited defects of vitamin B12 metabolism, in Olson RE, Bentler E, Broquist HP (eds): Annual Review ofNutrition. Palo Alto;Cooper BA;Calif,1987

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