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W G Sherwood

Showing results (1-10 of 37) with videos related to

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Journal of the American Dietetic Association|June 1, 1987
Current practices and improved recommendations for treating hereditary fructose intoleranceL Bell, W G Sherwood
Clinical Chemistry|May 1, 1993
3-Hydroxydicarboxylic and 3-ketodicarboxylic aciduria in three patients: evidence for a new defect in fatty acid oxidation at the level of 3-ketoacyl-CoA thiolaseM J Bennett, W G Sherwood
Journal of Inherited Metabolic Disease|January 1, 1984
Lactic acidaemiaB H Robinson, W G Sherwood
Pediatric Research|December 1, 1975
Pyruvate dehydrogenase phosphatase deficiency: a cause of congenital chronic lactic acidosis in infancyB H Robinson, W G Sherwood
Journal of Inherited Metabolic Disease|January 1, 1985
Multiple acyl-CoA dehydrogenase deficiency: a neonatal onset case responsive to treatmentZ H Verjee, W G Sherwood
Biology of the Neonate|January 1, 1977
The development of pyruvate dehydrogenase in the subhuman primate Macaca mulattaB H Robinson, W G Sherwood, J Oei
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 Sherwood
European Journal of Pediatrics|June 1, 1990
Partial biotinidase deficiency associated with Coffin-Siris syndromeA B Burlina, W G Sherwood, F Zacchello
Pediatric Research|August 1, 1980
The genetic heterogeneity of lactic acidosis: occurrence of recognizable inborn errors of metabolism in pediatric population with lactic acidosisB H Robinson, J Taylor, W G Sherwood
Pediatric Research|December 1, 1977
Deficiency of dihydrolipoyl dehydrogenase (a component of the pyruvate and alpha-ketoglutarate dehydrogenase complexes): a cause of congenital chronic lactic acidosis in infancyB H Robinson, J Taylor, W G Sherwood
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
Journal of the American Dietetic Association|June 1, 1987
Current practices and improved recommendations for treating hereditary fructose intoleranceL Bell, W G Sherwood
Clinical Chemistry|May 1, 1993
3-Hydroxydicarboxylic and 3-ketodicarboxylic aciduria in three patients: evidence for a new defect in fatty acid oxidation at the level of 3-ketoacyl-CoA thiolaseM J Bennett, W G Sherwood
Journal of Inherited Metabolic Disease|January 1, 1984
Lactic acidaemiaB H Robinson, W G Sherwood
Pediatric Research|December 1, 1975
Pyruvate dehydrogenase phosphatase deficiency: a cause of congenital chronic lactic acidosis in infancyB H Robinson, W G Sherwood
Journal of Inherited Metabolic Disease|January 1, 1985
Multiple acyl-CoA dehydrogenase deficiency: a neonatal onset case responsive to treatmentZ H Verjee, W G Sherwood
Biology of the Neonate|January 1, 1977
The development of pyruvate dehydrogenase in the subhuman primate Macaca mulattaB H Robinson, W G Sherwood, J Oei
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 Sherwood
European Journal of Pediatrics|June 1, 1990
Partial biotinidase deficiency associated with Coffin-Siris syndromeA B Burlina, W G Sherwood, F Zacchello
Pediatric Research|August 1, 1980
The genetic heterogeneity of lactic acidosis: occurrence of recognizable inborn errors of metabolism in pediatric population with lactic acidosisB H Robinson, J Taylor, W G Sherwood
Pediatric Research|December 1, 1977
Deficiency of dihydrolipoyl dehydrogenase (a component of the pyruvate and alpha-ketoglutarate dehydrogenase complexes): a cause of congenital chronic lactic acidosis in infancyB H Robinson, J Taylor, W G Sherwood
Pageof 4