Protein substitute for children and adults with phenylketonuria
Author:
Affiliation:
1. Emory Genetics Metabolic Nutrition Program; 2165 N. Decatur Road Decatur Georgia USA 30033
2. Emory University School of Medicine; Department of Human Genetics; 2165 North Decatur Road Decatur Georgia USA 30033
Publisher
Wiley
Subject
Pharmacology (medical)
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/14651858.CD004731.pub4/fullpdf
Reference81 articles.
1. Protein substitute dosage in PKU: how much do young patients need?;MacDonald;Archives of Disease in Childhood,2006
2. MacDonald A Daly A Chakrapani A Rylance G Asplin D Hall SK What is the ideal dose of protein substitute in PKU? SHS Inborn Error Review Series 2003 15
3. A new amino acid mixture permits new approaches to the treatment of phenylketonuria;Buist;Acta Paediatrica,1994
4. Treatment products and approaches for phenylketonuria: improved palatability and flexibility demonstrate safety, efficacy and acceptance in US clinical trials;Prince;Journal of Inherited Metabolic Disease,1997
5. The effects of large neutral amino acid supplements in PKU: an MRS and neuropsychological study;Schindeler;Molecular Genetics and Metabolism,2007
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