Complementary dietary treatment using lysine-free, arginine-fortified amino acid supplements in glutaric aciduria type I — A decade of experience
- 1 September 2012
- journal article
- Published by Elsevier BV in Molecular Genetics and Metabolism
- Vol. 107 (1-2), 72-80
- https://doi.org/10.1016/j.ymgme.2012.03.021
Abstract
No abstract availableKeywords
Funding Information
- Kindness-for-Kids Foundation
- European Commission
This publication has 63 references indexed in Scilit:
- Glutaric Aciduria Type 1 Metabolites Impair the Succinate Transport from Astrocytic to Neuronal CellsOnline Journal of Public Health Informatics, 2011
- Diagnosis and management of glutaric aciduria type I – revised recommendationsJournal of Inherited Metabolic Disease, 2011
- Disorders of creatine transport and metabolismSeminars in Medical Genetics, Part C of the American Journal of Medical Genetics, 2011
- Glutaric aciduria type I: outcome following detection by newborn screeningJournal of Inherited Metabolic Disease, 2008
- Mechanism of age-dependent susceptibility and novel treatment strategy in glutaric acidemia type IJCI Insight, 2007
- Perzentile für den Body-mass-Index für das Kindes- und Jugendalter unter Heranziehung verschiedener deutscher StichprobenMonatsschrift Kinderheilkunde, 2001
- Arginine-responsive asymptomatic hyperammonemia in the premature infantThe Journal of Pediatrics, 1984
- Treatment of Episodic Hyperammonemia in Children with Inborn Errors of Urea SynthesisThe New England Journal of Medicine, 1984
- Treatment of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria): Experience with diet, riboflavin, and GABA analogueThe Journal of Pediatrics, 1979
- Glutaric aciduria: Biochemical and morphologic considerationsThe Journal of Pediatrics, 1977