Nutrition support for glutaric acidemia type I
Author:
Publisher
Elsevier BV
Subject
Nutrition and Dietetics,Food Science
Reference51 articles.
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3. Glutaryl-coenzyme A dehydrogenase deficiency: a distinct encephalopathy;Hoffman;Pediatrics,1991
4. Clinical and biochemical studies in three sibs with glutaric aciduria type I response to dietary therapy;Warman;Am J Hum Genet,1988
5. Studies on glutaryl-Co-A dehydrogenase in leucocytes, fibroblasts and amniotic fluid cells: the normal enzyme and the mutant form in patients with glutaric aciduria;Christensen;Clin Chim Acta,1978
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1. Two novel compound heterozygous variants of the GCDH gene in two Chinese families with glutaric acidaemia type I identified by high-throughput sequencing and a literature review;Molecular Genetics and Genomics;2023-03-11
2. Recommendations for diagnosing and managing individuals with glutaric aciduria type 1: Third revision;Journal of Inherited Metabolic Disease;2022-11-17
3. The Challenge of Severe Acute Malnutrition in Inborn Errors of Metabolism: Does Medical Food Alone Suffice?;Journal of Pediatric Genetics;2022-05-05
4. Inconsistencies in the Nutrition Management of Glutaric Aciduria Type 1: An International Survey;Nutrients;2020-10-16
5. Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision;Journal of Inherited Metabolic Disease;2016-11-16
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