A case of glutaric acidemia type I: Effect of riboflavin and carnitine
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference15 articles.
1. Glutaric aciduria: a “new” disorder of amino acid metabolism;Goodman;Biochem Med,1975
2. Glutaric aciduria: inherited deficiency of glutaryl-CoA dehydrogenase activity;Goodman;Biochem Med,1975
3. Treatment of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria): experience with diet, riboflavin, and GABA analogue;Brandt;J Pediatr,1979
4. l-Carnitine treatment in glutaric aciduria type I;Seccombe;Neurology,1986
5. Glutaric acidemia: a metabolic disorder causing progressive choreoathetosis;Leibel;Neurology,1980
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1. Recommendations for diagnosing and managing individuals with glutaric aciduria type 1: Third revision;Journal of Inherited Metabolic Disease;2022-11-17
2. Glutaric aciduria type 1: Typical aspects in imaging;Edorium Journal of Radiology;2022-10-11
3. Functional Recovery of a GCDH Variant Associated to Severe Deflavinylation—Molecular Insights into Potential Beneficial Effects of Riboflavin Supplementation in Glutaric Aciduria-Type I Patients;International Journal of Molecular Sciences;2020-09-25
4. Glutaric Aciduria Type 1: A Case Report and Review of Literature;Journal of Pediatric Intensive Care;2020-04-17
5. Riboflavin (vitamin B2) and mitochondrial energy;Molecular Nutrition;2020
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