Interrupting the mechanisms of brain injury in a model of maple syrup urine disease encephalopathy

Author:

Zinnanti William J.,Lazovic Jelena

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference47 articles.

1. Chuang DT, Shih VE (2001) Maple syrup urine disease (branched-chain ketoaciduria). In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic and molecular bases of inherited disease. McGraw-Hill, New York, pp 1971–2005

2. Chuang DT, Ku LS et al (1982) Biochemical basis of thiamin-responsive maple syrup urine disease. Trans Assoc Am Physicians 95:196–204

3. Cremer JE (1982) Substrate utilization and brain development. J Cereb Blood Flow Metab 2(4):394–407

4. Crome L, Dutton G et al (1961) Maple syrup urine disease. J Pathol Bacteriol 81:379–384

5. Dancis J, Hutzler J et al (1960) Metabolism of the white blood cells in maple-syrup-urine disease. Biochim Biophys Acta 43:342–343

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