Is the Oral Methionine Loading Test Insensitive to the Remethylation Pathway of Homocysteine?
Author:
Affiliation:
1. A. Bianchi Bonomi Hemophilia and Thrombosis Center, Department of Internal Medicine, IRCCS Ospedale Maggiore, University of Milano, Milano, Italy
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/93/3/1118/1651084/1118.pdf
Reference11 articles.
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2. A common mutation in the methylene-tetrahydrofolate reductase gene (C677T) increases the risk for deep-vein thrombosis in patients with mutant factor V (factor V:Q506).;Cattaneo;Arterioscler Thromb Vasc Biol,1997
3. Hyperhomocyst(e)inemia and a common methylenetetrahydrofolate reductase mutation (Ala223Val MTHFR) in patients with inherited thrombophilic coagulation defects.;Legnani;Arterioscler Thromb Vasc Biol,1997
4. Common mutation in the methylenetetrahydrofolate reductase gene offers no support for mild hyperhomocysteinemia being a causal risk factor for cardiovascular disease.;Brattström;Circulation,1997
5. The 677C → T mutation in the methylenetetrahydrofolate reductase gene: Associations with plasma total homocysteine levels and risk of coronary atherosclerotic disease.;Verhoef;Atherosclerosis,1997
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