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70Biochemical studies in a patient with defects in the metabolism of acyl-CoA and sarcosine: Another possible case of glutaric aciduria type II, Journal of Inherited Metabolic Disease A case of biotin-responsive 3-methylcrotonylglycin- and 3-hydroxyisovaleric aciduria, European Journal of Pediatrics 3-HMG Coenzyme A Lyase Deficiency: Macrocephaly and Left Ventricular Noncompaction with a Novel Mutation, The Indian Journal of Pediatrics Isolated 3-methylcrotonyl-coenzyme A carboxylase deficiency in a child with metabolic stroke, Journal of Inherited Metabolic Disease 3-Hydroxyisovalerylcarnitine in 3-methylcrotonyl-CoA carboxylase deficiency, Journal of Inherited Metabolic Disease Isolated (biotin-resistant) 3-methylcrotonyl-CoA carboxylase deficiency: four sibs devoid of pathology, Journal of Inherited Metabolic Disease Glycine andl-carnitine therapy in 3-methylcrotonyl-CoA carboxylase deficiency, Journal of Inherited Metabolic Disease Acylcarnitine profile in tissues and body fluids of biotin-deficient rats with and withoutl-carnitine supplementation, Journal of Inherited Metabolic Disease Screening for defects of branched-chain amino acid metabolism, European Journal of Pediatrics Variable clinical presentation in three patients with 3-methylglutaconyl-coenzyme A hydratase deficiency, Journal of Inherited Metabolic Disease