Showing results (1-10 of 8) with videos related to
Sort By:
Pageof 1
Molecular Pharmacology|June 1, 1987
Defective induction of phenol glucuronidation by 3-methylcholanthrene in Gunn rats is due to the absence of a specific UDP-glucuronosyltransferase isoenzymeM W Coughtrie, B Burchell, I M Shepherd, et al.Annals of Neurology|November 1, 1990
Absence of immunoreactive enzyme protein in short-chain acylcoenzyme A dehydrogenase deficiencyL Farnsworth, I M Shepherd, M A Johnson, et al.Journal of Inherited Metabolic Disease|January 1, 1987
Defects of fatty acid oxidation in skeletal muscleD M Turnbull, K Bartlett, N J Watmough, et al.FEBS Letters|December 5, 1988
A case of carnitine palmitoyltransferase II deficiency in human skeletal muscleR Singh, I M Shepherd, J P Derrick, et al.Brain : a Journal of Neurology|August 1, 1988
Lipid storage myopathy associated with low acyl-CoA dehydrogenase activitiesD M Turnbull, I M Shepherd, B Ashworth, et al.Journal of Inherited Metabolic Disease|January 1, 1988
Fatal lactic acidosis due to deficiency of E1 component of the pyruvate dehydrogenase complexM A Birch-Machin, I M Shepherd, M Solomon, et al.Journal of the Neurological Sciences|November 1, 1988
Cytochrome oxidase deficiency: immunological studies of skeletal muscle mitochondrial fractionsI M Shepherd, M A Birch-Machin, M A Johnson, et al.Pediatric Research|May 1, 1989
Fatal lactic acidosis in infancy with a defect of complex III of the respiratory chainM A Birch-Machin, I M Shepherd, N J Watmough, et al.Pageof 1