Executive functioning in context: Relevance for treatment and monitoring of phenylketonuria-Reference-Cited by-同舟云学术

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Executive functioning in context: Relevance for treatment and monitoring of phenylketonuria

Published:2013 Issue: Volume:110 Page:S25-S30
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Huijbregts Stephan C.J.,Gassió Rosa,Campistol Jaume

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference82 articles.

1. Hyperphenylalaninemia: phenylalanine hydroxylase deficiency;Scriver,2001

2. Phenylketonuria;Blau;Lancet,2010

3. Phenylketonuria: an unfolding story;Thompson,1995

4. Pathophysiology of phenylketonuria;Dyer;Ment. Retard. Dev. Disabil. Res. Rev.,1999

5. Diffusion-weighted imaging of white matter abnormalities in patients with Phenylketonuria;Philips;Am. J. Neuroradiol.,2001

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1. Children and Adolescents with Early Treated Phenylketonuria: Cognitive Development and Fluctuations of Blood Phenylalanine Levels;International Journal of Environmental Research and Public Health;2024-04-02

2. The effects of phenylalanine and tyrosine levels on dopamine production in rat PC12 cells. Implications for treatment of phenylketonuria, tyrosinemia type 1 and comorbid neurodevelopmental disorders;Neurochemistry International;2023-12

3. Executive functions in preschool children with moderate hyperphenylalaninemia and phenylketonuria: a prospective study;Orphanet Journal of Rare Diseases;2023-07-03

4. Neuropsychological and quality of life outcomes in PKU patients: expert recommendations of assessment tools in Brazil;Arquivos de Neuro-Psiquiatria;2023-06-19

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