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8Susan C. ConnorCurrent address: Cambridge University, Biochemistry Department, Hopkins Building, Tennis Court Road, Cambridge, UK. E-mail: susan.c.connor@googlemail.com., Michael K. HansenCurrent address: Discovery Research, Wyeth, 500 Arcola Road, Collegeville, PA 19426, USA., Adam Corner, Randall F. Smith and Terence E. Ryan.
Integration of metabolomics and transcriptomics data to aid biomarker discovery in type 2 diabetes, Mol. Biosyst., 2010, 6, 909. Urinary excretion of 2-methylacetoacetate, 2-methyl-3-hydroxybutyrate and tiglylglycine after isoleucine loading in the diagnosis of 2-methylacetoacetyl-CoA thiolase deficiency, 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 Enzymology of the branched-chain amino acid oxidation disorders: the valine pathway, Journal of Inherited Metabolic Disease Muscle cytochromec oxidase deficiency accompanied by a urinary organic acid pattern mimicking multiple acyl-CoA dehydrogenase deficiency, 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 Isobutyryl-CoA dehydrogenase deficiency: Isobutyrylglycinuria and ACAD8 gene mutations in two infants, Journal of Inherited Metabolic Disease