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23A case of ??-ketothiolase deficiency, Journal of Inherited Metabolic Disease Late onset type of propionic acidaemia: Case report and biochemical studies, Journal of Inherited Metabolic Disease Clinical and molecular analysis of 6 Chinese patients with isoleucine metabolism defects: identification of 3 novel mutations in the HSD17B10 and ACAT1 gene, Metabolic Brain Disease Phenotypically mild presentation in a patient with 2-methylacetoacetyl-coenzyme A (??-keto)thiolase deficiency, Journal of Inherited Metabolic Disease Inhibition of energy metabolism by 2-methylacetoacetate and 2-methyl-3-hydroxybutyrate in cerebral cortex of developing rats, Journal of Inherited Metabolic Disease A new case of 2-methylacetoacetyl-CoA thiolase deficiency?, Journal of Inherited Metabolic Disease Identification of heteroxygotes for the defect of mitochondrial 3-ketoacyl-CoA thiolase causing 2-methyl-3-hydroxybutyric aciduria, Journal of Inherited Metabolic Disease ??-Ketothiolase deficiency: Two siblings with different clinical conditions, Journal of Inherited Metabolic Disease Propionyl-CoA carboxylase deficiency with overflow of metabolites of isoleucine catabolism at all levels, European Journal of Pediatrics Mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency: An inborn error of isoleucine and ketone body metabolism, Journal of Inherited Metabolic Disease