Update on Dietary Compliance, Nutritional Status, and Neuropsychological Functioning in the Chilean Phenylketonuria cohort
Author:
Affiliation:
1. Universidad de Chile
Publisher
FapUNIFESP (SciELO)
Subject
Genetics (clinical),Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health
Link
http://www.scielo.br/pdf/jiems/v9/2326-4594-jiems-9-e20210003.pdf
Reference45 articles.
1. Errores innatos en el metabolismo del niño,2017
2. Phenylketonuria;Blau N;The Lancet,2010
3. Past, present and future of newborn screening in Chile;Cornejo V;J Inherit Metab Dis,2010
4. Recommendations for the nutrition management of phenylalanine hydroxylase deficiency;Singh RH;Genet Med,2014
5. Updated, web-based nutrition management guideline for PKU: An evidence and consensus based approach;Singh RH;Mol Genet Metab,2016
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1. Evaluating Therapy and Growth in Children with Phenylketonuria: A Retrospective Longitudinal Study from Two Romanian Centers;Medicina;2024-07-22
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3. Need analysis of a dietary application among caregivers of patients with disorders of amino acid metabolism (AAMDs): A mixed-method approach;International Journal of Medical Informatics;2023-09
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