Cargando…
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...
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: | |
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 |
Ejemplares similares
-
Comparison of Glycomacropeptide with Phenylalanine Free-Synthetic Amino Acids in Test Meals to PKU Patients: No Significant Differences in Biomarkers, Including Plasma Phe Levels
por: Ahring, Kirsten K., et al.
Publicado: (2018) -
PKU dietary handbook to accompany PKU guidelines
por: MacDonald, A., et al.
Publicado: (2020) -
Correction to: PKU dietary handbook to accompany PKU guidelines
por: MacDonald, A., et al.
Publicado: (2020) -
Multiclinic Observations on the Simplified Diet in PKU
por: Bernstein, Laurie, et al.
Publicado: (2017) -
Is the Phenylalanine-Restricted Diet a Risk Factor for Overweight or Obesity in Patients with Phenylketonuria (PKU)? A Systematic Review and Meta-Analysis
por: Rodrigues, Catarina, et al.
Publicado: (2021)