The role of the blood-brain barrier in the aetiology of permanent brain dysfunction in hyperphenylalaninaemia

Author:

Hommes F. A.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference32 articles.

1. Baños, G., Daniel, P. M., Moorhouse, S. R. and Pratt, O. E. Inhibition of entry of some amino acids into the brain with observations on mental retardation in the amino acidurias.Psychol. Med. 4 (1977) 262–270

2. Berger, R., Springer, J. and Hommes, F. A. Brain protein and myelin metabolism in young hyperphenylalaninemic rats.Mol. Cell Biol. 26 (1980) 31–36

3. Berry, H. K., Bofinger, M. K., Hunt, M. M., Phillips, P. J. and Guilfaile, M. B. Reduction of cerebrospinal fluid phenylalanine after oral administration of valine, isoleucine and leucine.Pediatr. Res. 16 (1982) 751–755

4. Berry, H. K., Jordan, M. K., Brunner, R. L. and Hunt, M. M. Preliminary support for the oral administration of valine, isoleucine and leucine for phenylketonuria.Dev. Med. Child. Neurol. 27 (1985) 33–39

5. Buist, N. R. M., Kennaway, N. G. and Fellman, J. H. Tyrosinemia type II: hepatic cytsol tyrosine aminotransferase deficiency (The ‘Richner-Hahnart Syndrome’). In Bickel, H. and Wachtel, U. (eds)Inherited Diseases of Amino Acid Metabolism. Recent Progress in the Understanding, Recognition and Management, Thieme Verlag, Stuttgart, 1985, pp. 203–235

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