Long-term treatment of phenylketonuria with a new medical food containing large neutral amino acids

BACKGROUND/OBJECTIVES: Phenylketonuria (PKU) is an autosomal recessive disease caused by deficient activity of phenylalanine hydroxylase. A low phenylalanine (Phe) diet is used to treat PKU. The diet is very restrictive, and dietary adherence tends to decrease as patients get older. Methods to impro...

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Veröffentlicht in:Eur J Clin Nutr
Hauptverfasser: Concolino, D, Mascaro, I, Moricca, M T, Bonapace, G, Matalon, K, Trapasso, J, Radhakrishnan, G, Ferrara, C, Matalon, R, Strisciuglio, P
Format: Artigo
Sprache:Inglês
Veröffentlicht: Nature Publishing Group 2017
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Original Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5222990/
https://ncbi.nlm.nih.gov/pubmed/27623981
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejcn.2016.166
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