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Progress in Clinical and Biological Research
|
January 1, 1990
Fatty acid oxidation defects as causes of unexpected death in infancy
M J Bennett, F Allison, R J Pollitt, et al.
British Journal of Cancer
|
September 1, 1976
Successful pregnancy in acute monocytic leukaemia
R Gokal, J Durrant, J D Baum, et al.
Journal of Inherited Metabolic Disease
|
July 1, 1997
Hypoketonuric 3-hydroxydicarboxylic aciduria in five patients with glycogen storage disease
C E Mize, L J Waber, T Anderson, et al.
Clinical Chemistry
|
May 1, 1984
Cyclosporin concentrations in whole blood and plasma
M J Bennett, K H Carpenter, E Worthy, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 15, 1992
Abnormal lysosomal cathepsin activities in leukocytes and cultured skin fibroblasts in late infantile, but not in juvenile neuronal ceroid-lipofuscinosis (Batten disease)
M J Bennett, L Chern, K H Carpenter, et al.
British Journal of Anaesthesia
|
April 1, 1976
Haemodynamic interactions of high-dose propranolol pretreatment and anaesthesia in the dog. I: Halothane dose-response studies
J G Roberts, P Foëx, T N Clarke, et al.
Biochemical and Biophysical Research Communications
|
April 6, 1995
Intact alpha-subunit is required for membrane-binding of human mitochondrial trifunctional beta-oxidation protein, but is not necessary for conferring 3-ketoacyl-CoA thiolase activity to the beta-subunit
M J Weinberger, P Rinaldo, A W Strauss, et al.
European Journal of Pediatrics
|
October 1, 1986
Glutaric aciduria type 1: biochemical investigations and postmortem findings
M J Bennett, N Marlow, R J Pollitt, et al.
Clinical Chemistry
|
September 1, 1990
Medium-chain acyl-CoA dehydrogenase deficiency: a useful diagnosis five years after death
M J Bennett, R J Pollitt, L S Taitz, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Azelaic and pimelic acids: metabolic intermediates or artefacts?
M J Bennett, M C Ragni, I Hood, et al.
Page
of 36
Search research articles
Search
Showing results (151-160 of 351) with videos related to
Sort By:
Page
of 36
Progress in Clinical and Biological Research
|
January 1, 1990
Fatty acid oxidation defects as causes of unexpected death in infancy
M J Bennett, F Allison, R J Pollitt, et al.
British Journal of Cancer
|
September 1, 1976
Successful pregnancy in acute monocytic leukaemia
R Gokal, J Durrant, J D Baum, et al.
Journal of Inherited Metabolic Disease
|
July 1, 1997
Hypoketonuric 3-hydroxydicarboxylic aciduria in five patients with glycogen storage disease
C E Mize, L J Waber, T Anderson, et al.
Clinical Chemistry
|
May 1, 1984
Cyclosporin concentrations in whole blood and plasma
M J Bennett, K H Carpenter, E Worthy, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 15, 1992
Abnormal lysosomal cathepsin activities in leukocytes and cultured skin fibroblasts in late infantile, but not in juvenile neuronal ceroid-lipofuscinosis (Batten disease)
M J Bennett, L Chern, K H Carpenter, et al.
British Journal of Anaesthesia
|
April 1, 1976
Haemodynamic interactions of high-dose propranolol pretreatment and anaesthesia in the dog. I: Halothane dose-response studies
J G Roberts, P Foëx, T N Clarke, et al.
Biochemical and Biophysical Research Communications
|
April 6, 1995
Intact alpha-subunit is required for membrane-binding of human mitochondrial trifunctional beta-oxidation protein, but is not necessary for conferring 3-ketoacyl-CoA thiolase activity to the beta-subunit
M J Weinberger, P Rinaldo, A W Strauss, et al.
European Journal of Pediatrics
|
October 1, 1986
Glutaric aciduria type 1: biochemical investigations and postmortem findings
M J Bennett, N Marlow, R J Pollitt, et al.
Clinical Chemistry
|
September 1, 1990
Medium-chain acyl-CoA dehydrogenase deficiency: a useful diagnosis five years after death
M J Bennett, R J Pollitt, L S Taitz, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Azelaic and pimelic acids: metabolic intermediates or artefacts?
M J Bennett, M C Ragni, I Hood, et al.
Page
of 36