A diversified approach for PKU treatment: Routine screening yields high incidence of psychiatric distress in phenylketonuria clinics-Reference-Cited by-同舟云学术

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A diversified approach for PKU treatment: Routine screening yields high incidence of psychiatric distress in phenylketonuria clinics

Published:2013-01 Issue:1 Volume:108 Page:8-12
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Burton Barbara K.,Leviton Lauren,Vespa Hazel,Coon Hilary,Longo Nicola,Lundy Bridget D.,Johnson Maria,Angelino Andrew,Hamosh Ada,Bilder Deborah

Publisher

Elsevier BV

Subject

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

Reference21 articles.

1. The PAH gene, phenylketonuria, and a paradigm shift;Scriver;Hum. Mutat.,2007

2. The neuropathology of phenylketonuria: human and animal studies;Huttenlocher;Eur. J. Pediatr.,2000

3. Inhibitory control in children with phenylketonuria;Christ;Dev. Neuropsychol.,2006

4. Age-related working memory impairments in children with prefrontal dysfunction associated with phenylketonuria;White;J. Int. Neuropsychol. Soc.,2002

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1. Disease Management in Individuals with Phenylketonuria;Clinical and Experimental Health Sciences;2024-06-28

2. The relationship between working memory and anxiety in individuals with early treated phenylketonuria (PKU).;Neuropsychology;2024-05

3. Pharmacodynamics, safety, tolerability and pharmacokinetics of a single oral dose of an engineered phenylalanine ammonia-lyase in patients with phenylketonuria;Molecular Genetics and Metabolism Reports;2023-12

4. Inborn errors of amino acid metabolism – from underlying pathophysiology to therapeutic advances;Disease Models & Mechanisms;2023-11-01

5. Genotypic variants of the tetrahydrobiopterin (BH4) biosynthesis genes in patients with hyperphenylalaninemia from different regions of Iran;Molecular Genetics & Genomic Medicine;2023-10-11

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