Long-term use of investigational β-Hydroxybutyrate salts in children with multiple acyl-CoA dehydrogenase or pyruvate dehydrogenase deficiency-Reference-Cited by-同舟云学术

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Long-term use of investigational β-Hydroxybutyrate salts in children with multiple acyl-CoA dehydrogenase or pyruvate dehydrogenase deficiency

Published:2024-09 Issue: Volume:40 Page:101104
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Morris Andrew A.M.,Cuenoud Bernard,Delerive Philippe,Mundy Helen,Schwahn Bernd C.

Funder

Nestlé Health Science

Publisher

Elsevier BV

Reference24 articles.

1. Neonatal-onset multiple acyl-CoA dehydrogenase deficiency (MADD) in the ETFDH gene: A case report and a literature review;Ding;Medicine (Baltimore),2020

2. Multiple Acyl-CoA Dehydrogenase Deficiency;Prasun,2020

3. Cystic renal dysplasia as a leading sign of inherited metabolic disease;Distelmaier;Pediatr. Nephrol.,2007

4. Clinical, biochemical, and genetic heterogeneity in Glutaric aciduria type II patients;Ali;Genes (Basel),2021

5. Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency;Fu;Neurol. Sci.,2016

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