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Journal of Inherited Metabolic Disease|January 1, 1994
6-Methyluracil excretion in 2-methylacetoacetyl-CoA thiolase deficiency and in two children with an unexplained recurrent ketoacidaemiaC H Cromby, N J Manning, R J Pollitt, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorderM J Bennett, R J Pollitt, S I Goodman, et al.
British Journal of Anaesthesia|December 1, 1977
Haemodynamic responses to isoflurane anaesthesia and hypovolaemia in the dog, and their modification by propranololB F Horan, C Prys-Roberts, J G Roberts, et al.
British Journal of Anaesthesia|March 1, 1980
Circulatory responses of the dog to acute isovolumic anaemia in the presence of high-grade adrenergic beta-receptor blockadeT N Clarke, P Foëx, J G Roberts, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Biochemical investigations on a patient with a defect in cytosolic acetoacetyl-CoA thiolase, associated with mental retardationM J Bennett, G P Hosking, M F Smith, et al.
Biochemistry|August 20, 1996
Structure of 3 alpha-hydroxysteroid/dihydrodiol dehydrogenase complexed with NADP+M J Bennett, B P Schlegel, J M Jez, et al.
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