Glycine therapy in isovaleric acidemia
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference18 articles.
1. Isovaleric acidemia. Clinical features of a new genetic defect of leucine metabolism;Budd;N Engl J Med,1967
2. Isovaleric acidemia: Results of a family study and dietary treatment;Levy;Pediatrics,1973
3. An inborn error of short-chain fatty acid metabolism;Sidbury;J Pediatr,1967
4. Neonatal death associated with isovaleric acidemia;Newman;Lancet,1967
5. Therapeutic effects of glycine in isovaleric acidemia;Krieger;Pediatr Res,1976
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1. The glycine N-acyltransferases, GLYAT and GLYATL1, contribute to the detoxification of isovaleryl-CoA - an in-silico and in vitro validation;Computational and Structural Biotechnology Journal;2023
2. Compound heterozygote variants: c.848A > G; p.Glu283Gly and c.890C > T; p.Ala297Val, of Isovaleric acid-CoA dehydrogenase (IVD) gene causing severe Isovaleric acidemia with hyperammonemia;Molecular Genetics and Metabolism Reports;2022-06
3. Acute encephalopathy in children in Muzaffarpur, India: a review of aetiopathogenesis;Transactions of The Royal Society of Tropical Medicine and Hygiene;2020-06-08
4. Aspects of Newborn Screening in Isovaleric Acidemia;International Journal of Neonatal Screening;2018-01-29
5. Enzymology of Amino Acid Conjugation Reactions;Comprehensive Toxicology;2018
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