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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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| Vydáno v: | Cochrane Database Syst Rev |
|---|---|
| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley & Sons, Ltd
2015
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| On-line přístup: | 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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