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Protein substitute for children and adults with phenylketonuria
BACKGROUND: Phenylketonuria is an inherited metabolic disorder characterised by an absence or deficiency of the enzyme phenylalanine hydroxylase. The aim of treatment is to lower blood phenylalanine concentrations to the recommended therapeutic range to prevent developmental delay and support normal...
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| Publicado no: | Cochrane Database Syst Rev |
|---|---|
| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley & Sons, Ltd
2015
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7212256/ https://ncbi.nlm.nih.gov/pubmed/25723866 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/14651858.CD004731.pub4 |
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