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Journal of the American Dietetic Association
|
June 1, 1987
Current practices and improved recommendations for treating hereditary fructose intolerance
L 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 thiolase
M J Bennett, W G Sherwood
Journal of Inherited Metabolic Disease
|
January 1, 1984
Lactic acidaemia
B H Robinson, W G Sherwood
Pediatric Research
|
December 1, 1975
Pyruvate dehydrogenase phosphatase deficiency: a cause of congenital chronic lactic acidosis in infancy
B H Robinson, W G Sherwood
Journal of Inherited Metabolic Disease
|
January 1, 1985
Multiple acyl-CoA dehydrogenase deficiency: a neonatal onset case responsive to treatment
Z H Verjee, W G Sherwood
Biology of the Neonate
|
January 1, 1977
The development of pyruvate dehydrogenase in the subhuman primate Macaca mulatta
B 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 deficiency
J Taylor, B H Robinson, W G Sherwood
European Journal of Pediatrics
|
June 1, 1990
Partial biotinidase deficiency associated with Coffin-Siris syndrome
A 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 acidosis
B 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 infancy
B H Robinson, J Taylor, W G Sherwood
Page
of 4
Search research articles
Search
Showing results (1-10 of 37) with videos related to
Sort By:
Page
of 4
Journal of the American Dietetic Association
|
June 1, 1987
Current practices and improved recommendations for treating hereditary fructose intolerance
L 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 thiolase
M J Bennett, W G Sherwood
Journal of Inherited Metabolic Disease
|
January 1, 1984
Lactic acidaemia
B H Robinson, W G Sherwood
Pediatric Research
|
December 1, 1975
Pyruvate dehydrogenase phosphatase deficiency: a cause of congenital chronic lactic acidosis in infancy
B H Robinson, W G Sherwood
Journal of Inherited Metabolic Disease
|
January 1, 1985
Multiple acyl-CoA dehydrogenase deficiency: a neonatal onset case responsive to treatment
Z H Verjee, W G Sherwood
Biology of the Neonate
|
January 1, 1977
The development of pyruvate dehydrogenase in the subhuman primate Macaca mulatta
B 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 deficiency
J Taylor, B H Robinson, W G Sherwood
European Journal of Pediatrics
|
June 1, 1990
Partial biotinidase deficiency associated with Coffin-Siris syndrome
A 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 acidosis
B 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 infancy
B H Robinson, J Taylor, W G Sherwood
Page
of 4