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Pediatric Research|January 1, 1978
A defect in branched-chain amino acid metabolism in a patient with congenital lactic acidosis due to dihydrolipoyl dehydrogenase deficiencyJ Taylor, B H Robinson, W G SherwoodBiochemistry|November 28, 1989
Sequence- and structure-dependent DNA base dynamics: synthesis, structure, and dynamics of site and sequence specifically spin-labeled DNAA Spaltenstein, B H Robinson, P B HopkinsPediatric Research|April 1, 1977
Deficient activity of hepatic pyruvate dehydrogenase and pyruvate carboxylase in Reye's syndromeB H Robinson, D G Gall, E CutzBiochimica Et Biophysica Acta|April 18, 1998
Saguenay Lac Saint Jean cytochrome oxidase deficiency: sequence analysis of nuclear encoded COX subunits, chromosomal localization and a sequence anomaly in subunit VIcN Lee, C Morin, G Mitchell, et al.Journal of Inherited Metabolic Disease|January 1, 1996
NADH-coenzyme Q reductase (complex I) deficiency: heterogeneity in phenotype and biochemical findingsS Pitkänen, A Feigenbaum, R Laframboise, et al.Critical Care Medicine|January 6, 1999
Lactic acidemia and bradyarrhythmia in a child sedated with propofolS H Cray, B H Robinson, P N CoxJournal of Inherited Metabolic Disease|January 1, 1996
Disorders of pyruvate carboxylase and the pyruvate dehydrogenase complexB H Robinson, N MacKay, K Chun, et al.Canadian Journal of Biochemistry|June 1, 1976
Properties of the citrate transporter in rat heart: implications for regulation of glycolysis by cytosolic citrateS Cheema-Dhadli, B H Robinson, M L HalperinMolecular and Cellular Endocrinology|April 1, 2006
Pyruvate dehydrogenase phosphatase deficiency: orphan disease or an under-diagnosed condition?M C Maj, J M Cameron, B H RobinsonThe Journal of Biological Chemistry|May 25, 1983
[3H]biotin-labeled proteins in cultured human skin fibroblasts from patients with pyruvate carboxylase deficiencyB H Robinson, J Oei, M Saunders, et al.Pageof 21