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Pediatric Research|February 1, 1983
Episodic hypoglycemia with psi-hydroxy fatty acid excretionE Colle, O A Mamer, J A Montgomery, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 15, 1983
Apparent gastrointestinal origin of cis-4-hydroxycyclohexanecarboxylic acidJ B Kronick, O A Mamer, J Montgomery, et al.
Analytical Biochemistry|March 10, 2001
Measurement of succinylcholine concentration in human plasma by electrospray tandem mass spectrometryJ J Roy, D Boismenu, H Gao, et al.
Lancet (London, England)|December 11, 1971
A "new" disorder of isoleucine catabolismR S Daum, P H Lamm, O A Mamer, et al.
The Biochemical Journal|December 15, 1976
Demonstration of a new mammalian isoleucine catabolic pathway yielding an Rseries of metabolitesO A Mamer, S S Tjoa, C R Scriver, et al.
The Journal of Nutrition|September 1, 1993
Alpha-keto and alpha-hydroxy branched-chain acid interrelationships in normal humansL J Hoffer, A Taveroff, L Robitaille, et al.
The American Journal of Physiology|June 1, 1997
Effects of leucine on whole body leucine, valine, and threonine metabolism in humansL J Hoffer, A Taveroff, L Robitaille, et al.
The Journal of Pediatrics|August 1, 1979
Acetoacetyl CoA thiolase deficiency: a cause of severe ketoacidosis in infancy simulating salicylismB H Robinson, W G Sherwood, J Taylor, et al.
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