Nutrient intake, body composition, and blood phenylalanine control in children with phenylketonuria compared to healthy controls
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology
Reference28 articles.
1. Positive effect of a simplified diet on blood phenylalanine control in different phenylketonuria variants, characterized by newborn BH4 loading test and PAH analysis;Zimmermann;Mol. Genet. Metab.,2012
2. Controlled diet in phenylketonuria and hyperphenylalaninemia may cause serum selenium deficiency in adult patients: the Czech experience;Prochazkova;Biol. Trace Elem. Res.,2013
3. Corrigendum to "Risk factors for developing mineral bone disease in phenylketonuric patients";Miras;Mol. Genet. Metab.,2013
4. Recommendations for the nutrition management of phenylalanine hydroxylase deficiency;Singh;Genet. Med.,2014
5. Management of phenylketonuria and hyperphenylalaninemia;de Baulny;J. Nutr.,2007
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