Glutaric acidemia type II: A form with deleterious intrauterine effects
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference18 articles.
1. Glutaric aciduria type II: Report on a previously undescribed metabolic disorder;Przyrembel;Clin Chim Acta,1976
2. Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria: Possible inherited deficiency of an electron transfer flavoprotein;Goodman;Pediatr Res,1980
3. Biochemical studies in a patient with defects in the metabolism of acyl-CoA and sarcosine: Another possible case of glutaric aciduria type II;Gregersen;J Inherited Metab Dis,1980
4. Glutaric aciduria type II;Sweetman;J Pediatr,1980
5. Glutaric acidemia type II: Clinical, biochemical and morphologic considerations;Goodman;J Pediatr,1982
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1. Prenatal presentation of glutaric aciduria type II: A case report with radiologic, clinical, biochemical, molecular, and pathological phenotyping;Clinical Case Reports;2021-01-12
2. Prenatal and foetal autopsy findings in glutaric aciduria type II;Birth Defects Research;2020-09-22
3. Hyperprolinemia in Type 2 Glutaric Aciduria and MADD-Like Profiles;JIMD Reports;2015
4. Mitochondrial Factors and VACTERL Association-Related Congenital Malformations;Molecular Syndromology;2013
5. Multiple acyl CoA dehydrogenase deficiency/glutaric aciduria type II/ethylmalonic-adipic aciduria;Atlas of Inherited Metabolic Diseases 3E;2011-12-30
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