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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.Annals of Clinical Biochemistry|January 1, 1994
Population screening for medium-chain acyl-CoA dehydrogenase deficiency: analysis of medium-chain fatty acids and acylglycines in blood spotsM J Bennett, M C Ragni, R J Ostfeld, 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.International Journal of Radiation Oncology, Biology, Physics|February 1, 1991
Marrow antioxidant enzyme activity in tumor-bearing and non-tumor-bearing mice following vincristine treatmentR M Johnke, D P Loven, R S Abernathy, et al.Journal of Inherited Metabolic Disease|January 1, 1991
Familial combined hyperlipidaemia: use of stable isotopes to demonstrate overproduction of very low-density lipoprotein apolipoprotein B by the liverJ A Cortner, P M Coates, M J Bennett, et al.Pediatric Pathology|November 1, 1991
Medium-chain acyl-CoA dehydrogenase deficiency: postmortem diagnosis in a case of sudden infant death and neonatal diagnosis of an affected siblingM J Bennett, P Rinaldo, D S Millington, et al.Archives of Pathology & Laboratory Medicine|July 1, 1997
Clinical, biochemical, and morphologic investigations of a case of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyR H Amirkhan, C F Timmons, K O Brown, et al.Neuropediatrics|November 1, 1990
Decreased erythrocyte and platelet phospholipids and fatty acids in juvenile neuronal ceroid-lipofuscinosis (Batten disease)M J Bennett, J H Galloway, I J Cartwright, et al.The Journal of Pediatrics|March 10, 2001
Molecular prenatal diagnosis in families with fetal mitochondrial trifunctional protein mutationsJ A Ibdah, Y Zhao, J Viola, et al.Pageof 25