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The Journal of Clinical Endocrinology and Metabolism|August 26, 1998
Regulation of biologically active dimeric inhibin A and B from infancy to adulthood in the maleW Byrd, M J Bennett, B R Carr, et al.
Bulletin Europeen De Physiopathologie Respiratoire|March 1, 1976
[CO2 "wash-out" : a factor contributing to increase myocardial performance in the face of hypoxia (author's transl)]P Foëx, C A Saner, R M Fordham, et al.
American Journal of Perinatology|April 1, 1996
Fetal polycystic kidney disease associated with glutaric aciduria type II: an inborn error of energy metabolismJ Whitfield, D Hurst, M J Bennett, et al.
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.
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