Psychological well‐being of early and continuously treated phenylketonuria patients
Author:
Affiliation:
1. Hospital for Children and Adolescents, Center for Pediatric Research Leipzig (CPL), Department of Women and Child Health, University Hospital, University of Leipzig Leipzig Germany
Funder
BioMarin Pharmaceutical
Merck KGaA
Publisher
Wiley
Subject
Biochemistry, Genetics and Molecular Biology (miscellaneous),Endocrinology, Diabetes and Metabolism,Internal Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/jmd2.12202
Reference46 articles.
1. The complete European guidelines on phenylketonuria: diagnosis and treatment
2. Assessment of the impact of phenylketonuria and its treatment on quality of life of patients and parents from seven European countries
3. Clinical burden of illness in patients with phenylketonuria (PKU) and associated comorbidities - a retrospective study of German health insurance claims data
4. Phenylketonuria in adulthood: A collaborative study
5. Depressive symptoms in adolescents with early and continuously treated phenylketonuria: Associations with phenylalanine and tyrosine levels
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1. The impact of a child’s inborn error of metabolism: the parents’ perspectives on restrictions, discrimination, family planning, and emergency management;Orphanet Journal of Rare Diseases;2024-08-26
2. Patient and carer perceptions of video, telephone and in-person clinics for Phenylketonuria (PKU);Orphanet Journal of Rare Diseases;2024-08-20
3. Life story of Iranian parents of a child with phenylketonuria: a qualitative study;Journal of Community Genetics;2023-06-06
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5. Psychopathological Risk Assessment in Children with Hyperphenylalaninemia;Children;2022-10-31
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