Dietary problems of phenylketonuria: Effect on CNS transmitters and their possible role in behaviour and neuropsychological function
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01799701
Reference23 articles.
1. Armstrong, M. D. and Robinson, K. S. On the excretion of indole derivatives in phenyl-ketonuria.Arch. Biochem. 52 (1954) 287–288
2. Berry, H. K., Bofinger, M. K., Melanie, M. H., Philips, P. J. and Guilfoile, M. B. Reduction of cerebrospinal fluid phenylalanine after oral administration of valine, isoleucine, and leucine.Pediatr. Res. 16 (1982) 751–755
3. Brunner, R. L., Jordan, M. K. and Berry, H. K. Early treated phenylketonuria: neuropsychologic consequences.J. Pediatr. 102 (1983) 831–835
4. Butler, L. J., O'Flynn, M. E., Seifert, W. E. and Howell, R. R. Neurotransmitter defects and treatment of disorders of hyperphenylalaninemia.J. Pediatr. 98 (1981) 729–733
5. Curtius, H. C., Vollmin, J. A. and Baerlocher, K. The use of deuterated phenylalanine for the elucidation of the phenylalanine-tyrosine meta10545sm.Clin. Chim. Acta 37 (1972) 277–285
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