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45Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiency, Journal of Inherited Metabolic Disease Increased oxidative stress in patients with 3-hydroxy-3-methylglutaric aciduria, Molecular and Cellular Biochemistry 3-Hydroxy-3-methylglutaric aciduria: Response to carnitine therapy and fat and leucine restriction, Journal of Inherited Metabolic Disease 3-Hydroxy-3-methylglutaric acid and orotic acid induced fatty liver in rats, Lipids Presence of Caffeic Acid in Flaxseed Lignan Macromolecule, Plant Foods for Human Nutrition Serum and liver lipid responses to 3-hydroxy-3-methylglutaric acid in rats on different carbohydrate diets, Lipids Incidence of 3-hydroxy-3-methylglutaryl-coenzyme A lyase (HL) deficiency in Brazil, South America, Journal of Inherited Metabolic Disease 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: review of 18 reported patients, European Journal of Pediatrics 3-Methylglutaconic aciduria: Report on a sibship with infantile progressive encephalopathy, European Journal of Pediatrics