Large neutral amino acids in the treatment of PKU: from theory to practice
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10545-010-9216-1
Reference39 articles.
1. Andersen AE, Avins L (1976) Lowering brain phenylalanine levels by giving other large neutral amino acids. A new experimental therapeutic approach to phenylketonuria. Arch Neurol 33:684–684
2. Berry HK, Bofinger MK, Hunt MM, Phillips PJ, Guilfoile MB (1982) Reduction of cerebrospinal fluid phenylalanine after oral administration of valine, isoleucine and leucine. Pediatr Res 16:751–755
3. Berry HK, Brunner RL, Hunt MM, White PP (1990) Valine, isoleucine and leucine. A new treatment for phenylketonuria. Am J Dis Child 144:539–543
4. Burlina AB, Bonafé L, Ferrari V, Suppiej A, Zacchello F, Burlina AP (2000) Measurement of neurotransmitter metabolites in the cerebrospinal fluid of phenylketonuric patients under dietary treatment. J Inherit Metab Dis 23:313–316
5. Butler IJ, O’Flynn ME, Seifert WE Jr, Howell RR (1981) Neurotransmitter defects and treatment of disorders of hyperphenylalaninemia. J Pediatr 98:729–733
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