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Metabolism: Clinical and Experimental|August 1, 1990
In vivo enzyme activity in inborn errors of metabolismG N Thompson, J H Walter, J V Leonard, et al.Lancet (London, England)|June 10, 1989
Contribution of aminoacid catabolism to propionate production in methylmalonic acidaemiaJ H Walter, G N Thompson, J V Leonard, et al.European Journal of Pediatrics|March 1, 1990
In vivo propionate oxidation as a prognostic indicator in disorders of propionate metabolismG N Thompson, J H Walter, J L Bresson, et al.The American Journal of Physiology|April 1, 1990
Protein and leucine metabolism in maple syrup urine diseaseG N Thompson, J L Bresson, P J Pacy, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|June 30, 1989
Measurement of propionate turnover in vivo using sodium [2H5]propionate and sodium [13C]propionateJ H Walter, G N Thompson, J V Leonard, et al.Metabolism: Clinical and Experimental|November 1, 1990
Sources of propionate in inborn errors of propionate metabolismG N Thompson, J H Walter, J L Bresson, et al.Journal of Inherited Metabolic Disease|January 1, 1994
Production and disposal of medium-chain fatty acids in children with medium-chain acyl-CoA dehydrogenase deficiencyS J Heales, G N Thompson, A F Massoud, et al.The Journal of Pediatrics|November 1, 1989
Substrate disposal in metabolic disease: a comparison between rates of in vivo propionate oxidation and urinary metabolite excretion in children with methylmalonic acidemiaG N Thompson, J H Walter, J L Bresson, et al.European Journal of Pediatrics|August 1, 1990
The use of metronidazole in management of methylmalonic and propionic acidaemiasG N Thompson, R A Chalmers, J H Walter, et al.The Journal of Clinical Investigation|July 1, 1990
Significant phenylalanine hydroxylation in vivo in patients with classical phenylketonuriaG N Thompson, D HallidayPageof 47