WITHDRAWN: Phenylalanine hydroxylase deficient phenylketonuria comparative metabolomics identifies energy pathway disruption and oxidative stress-Reference-Cited by-同舟云学术

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WITHDRAWN: Phenylalanine hydroxylase deficient phenylketonuria comparative metabolomics identifies energy pathway disruption and oxidative stress

Published:2021-04 Issue: Volume: Page:
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Dobrowolski Steven F.,Phua Yu Leng,Sudano Cayla,Spridik Kayla,Zinn Pascal O.,Wang Yudong,Bharathi Sivakama,Vockley Jerry,Goetzman Eric

Publisher

Elsevier BV

Subject

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

Reference66 articles.

1. A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants;Guthrie;Pediatrics.,1963

2. Influence of phenylalanine intake on phenylketonuria;Bickel;Lancet.,1953

3. Admissions of phenylketonuric patients to residential institutions before and after screening programs of the newborn infant;MacCready;J. Pediatr.,1974

4. The cardiovascular phenotype of adult patients with phenylketonuria;Azabdaftari;Orphanet J. Rare Dis.,2019

5. Bone health in phenylketonuria: a systematic review and meta-analysis;Demirdas;Orphanet J. Rare Dis.,2015

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1. New findings about neuropathological outcomes in the PKU mouse throughout lifespan;Molecular Genetics and Metabolism;2024-09

2. Whole-exome sequencing reveals genetic variants that may play a role in neurocytomas;Journal of Neuro-Oncology;2024-02

3. Characterization of phenylalanine hydroxylase gene variants and analysis of genotype–phenotype correlation in patients with phenylalanine hydroxylase deficiency from Fujian Province, Southeastern China;Molecular Biology Reports;2022-09-14

4. Untargeted metabolomic study of acute exacerbation of pediatric asthma via HPLC-Q-Orbitrap-MS;Journal of Pharmaceutical and Biomedical Analysis;2022-06

5. Domino liver transplant from a donor with maple syrup urine disease into a recipient with phenylketonuria;Molecular Genetics and Metabolism Reports;2022-06

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