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6Biochemical study of four cases of propionic acidaemia: GC/MS study of urinary metabolites, Journal of Inherited Metabolic Disease In vivo studies on the metabolic derangement in a patient with D-glyceric acidaemia and hyperglycinaemia, Journal of Inherited Metabolic Disease The occurrence of C6u2013C10-dicarboxylic acids, ethylmalonic acid, 5-hydroxycaproic acid, butyrylglycine, isovalerylglycine, isobutyrylglycine, 2-methylbutyrylglycine and glutaric acid in the urine of riboflavin deficient rats, Journal of Inherited Metabolic Disease Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two brothers, European Journal of Pediatrics Short/branched-chain acyl-CoA dehydrogenase deficiency due to an IVS3+3AG mutation that causes exon skipping, Human Genetics 2-methylbutyryl-CoA dehydrogenase deficiency associated with autism and mental retardation: a case report, Journal of Medical Case Reports