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Optimising amino acid absorption: essential to improve nitrogen balance and metabolic control in phenylketonuria

It has been nearly 70 years since the discovery that strict adherence to a diet low in phenylalanine prevents severe neurological sequelae in patients with phenylalanine hydroxylase deficiency (phenylketonuria; PKU). Today, dietary treatment with restricted phenylalanine intake supplemented with non...

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Detalhes bibliográficos
Publicado no:Nutr Res Rev
Main Authors: MacDonald, Anita, Singh, Rani H., Rocha, Júlio César, van Spronsen, Francjan J.
Formato: Artigo
Idioma:Inglês
Publicado em: Cambridge University Press 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6536823/
https://ncbi.nlm.nih.gov/pubmed/30284526
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/S0954422418000173
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