Multiclinic Observations on the Simplified Diet in PKU

Phenylketonuria is an inborn error of metabolism that historically has been treated with a strict phenylalanine-restricted diet where all foods are weighed and measured. This is cumbersome and difficult for patients and caregivers, especially patients with high phenylalanine blood concentrations who...

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Detalles Bibliográficos
Autores principales: Bernstein, Laurie, Burns, Casey, Sailer-Hammons, Melissa, Kurtz, Angela, Rohr, Frances
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615976/
https://www.ncbi.nlm.nih.gov/pubmed/29057118
http://dx.doi.org/10.1155/2017/4083293

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615976/
https://www.ncbi.nlm.nih.gov/pubmed/29057118
http://dx.doi.org/10.1155/2017/4083293

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