Adaptation and Validation of a Questionnaire to Evaluate Knowledge of the Low Phe Diet in PKU

Phenylketonuria (PKU) is an autosomal recessive disorder of phenylalanine (Phe) metabolism, causing a build-up of Phe in the body. Treatment consists of a Phe-restricted diet for life and regular determination of blood Phe levels to monitor the intake of Phe. Despite the fact that diet is the corner...

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Detalles Bibliográficos
Autores principales: Ramos-Álvarez, Rodolfo, Kapp, Maili, Rodríguez-Ruiz, María Mercedes, Fausor, Rocío, Bueno-Delgado, María Amor, Ahring, Kirsten, Waisbren, Susan E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8400675/
https://www.ncbi.nlm.nih.gov/pubmed/34444879
http://dx.doi.org/10.3390/nu13082719

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8400675/
https://www.ncbi.nlm.nih.gov/pubmed/34444879
http://dx.doi.org/10.3390/nu13082719

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