Dietary interventions for phenylketonuria
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Publisher
John Wiley & Sons, Ltd
Link
https://www.cochranelibrary.com/cdsr/doi/10.1002/14651858.CD001304/epdf/full
Reference41 articles.
1. Neuropsychological studies on adolescents with phenylketonuria returned to phenylalanine-restricted diets;Clarke;American Journal of Mental Retardation,1987
2. Transitory hyperphenylalaninaemia in children with continuously treated phenylketonuria;Griffiths;American Journal of Mental Retardation,1997
3. Neuropsychological outcome of experimental manipulation of phenylalanine intake in treated phenylketonuria;Griffiths;Journal of Inherited Metabolic Disease,1998
4. Termination of restricted diet in children with phenylketonuria: a randomised controlled study;Holtzman;New England Journal of Medicine,1975
5. Phenylalanine intakes of 1- to 6-year old children with phenylketonuria undergoing therapy;Acosta;American Journal of Clinical Nutrition,1983
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1. Measuring Burden of Illness in Phenylketonuria (PKU): Development of the PKU Symptom Severity and Impacts Scale as a Robust Patient-Reported Outcome;Advances in Therapy;2021-12-18
2. Dietary interventions for phenylketonuria;Cochrane Database of Systematic Reviews;2020-07-16
3. Development and psychometric validation of measures to assess the impact of phenylketonuria and its dietary treatment on patients’ and parents’ quality of life: the phenylketonuria – quality of life (PKU-QOL) questionnaires;Orphanet Journal of Rare Diseases;2015-05-10
4. Carnitine supplementation for inborn errors of metabolism;Cochrane Database of Systematic Reviews;2009-04-15
5. Inborn errors of metabolism: the flux from Mendelian to complex diseases;Nature Reviews Genetics;2006-06
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