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Progress in Clinical and Biological Research
|
January 1, 1990
Genetic defects of acyl-CoA dehydrogenases: studies using an electron transfer flavoprotein reduction assay
D E Hale, C A Stanley, P M Coates
Progress in Clinical and Biological Research
|
January 1, 1990
The long-chain acyl-CoA dehydrogenase deficiency
D E Hale, C A Stanley, P M Coates
Pediatric Research
|
May 1, 1988
Decreased fasting free fatty acids with L-carnitine in children with carnitine deficiency
W F Schwenk, D E Hale, M W Haymond
Digestive Diseases (Basel, Switzerland)
|
January 1, 1989
Progress in Reye syndrome: epidemiology, biochemical mechanisms and animal models
L Kilpatrick-Smith, D E Hale, S D Douglas
Progress in Clinical and Biological Research
|
January 1, 1990
Medium-chain acyl-CoA dehydrogenase deficiency
C A Stanley, D E Hale, P M Coates
Clinical Chemistry
|
February 1, 1997
Stability of long-chain and short-chain 3-hydroxyacyl-CoA dehydrogenase activity in postmortem liver
D E Hale, J E Cornell, M J Bennett
Cleveland Clinic Quarterly
|
March 19, 2010
The use of curare and pentothal sodium in endoscopy
H E HARRIS, R O LEWIS, D E HALE
Pediatric Research
|
September 1, 1991
Immunochemical characterization of variant long-chain acyl-CoA dehydrogenase in cultured fibroblasts from nine patients with long-chain acyl-CoA dehydrogenase deficiency
Y Indo, P M Coates, D E Hale, et al.
Analytical Biochemistry
|
May 1, 1990
An acyl-coenzyme A dehydrogenase assay utilizing the ferricenium ion
T C Lehman, D E Hale, A Bhala, et al.
Annals of Clinical Biochemistry
|
September 1, 1992
Comparison of post-mortem urinary and vitreous humour organic acids
M J Bennett, M C Ragni, I Hood, et al.
Page
of 9
Search research articles
Search
Showing results (11-20 of 85) with videos related to
Sort By:
Page
of 9
Progress in Clinical and Biological Research
|
January 1, 1990
Genetic defects of acyl-CoA dehydrogenases: studies using an electron transfer flavoprotein reduction assay
D E Hale, C A Stanley, P M Coates
Progress in Clinical and Biological Research
|
January 1, 1990
The long-chain acyl-CoA dehydrogenase deficiency
D E Hale, C A Stanley, P M Coates
Pediatric Research
|
May 1, 1988
Decreased fasting free fatty acids with L-carnitine in children with carnitine deficiency
W F Schwenk, D E Hale, M W Haymond
Digestive Diseases (Basel, Switzerland)
|
January 1, 1989
Progress in Reye syndrome: epidemiology, biochemical mechanisms and animal models
L Kilpatrick-Smith, D E Hale, S D Douglas
Progress in Clinical and Biological Research
|
January 1, 1990
Medium-chain acyl-CoA dehydrogenase deficiency
C A Stanley, D E Hale, P M Coates
Clinical Chemistry
|
February 1, 1997
Stability of long-chain and short-chain 3-hydroxyacyl-CoA dehydrogenase activity in postmortem liver
D E Hale, J E Cornell, M J Bennett
Cleveland Clinic Quarterly
|
March 19, 2010
The use of curare and pentothal sodium in endoscopy
H E HARRIS, R O LEWIS, D E HALE
Pediatric Research
|
September 1, 1991
Immunochemical characterization of variant long-chain acyl-CoA dehydrogenase in cultured fibroblasts from nine patients with long-chain acyl-CoA dehydrogenase deficiency
Y Indo, P M Coates, D E Hale, et al.
Analytical Biochemistry
|
May 1, 1990
An acyl-coenzyme A dehydrogenase assay utilizing the ferricenium ion
T C Lehman, D E Hale, A Bhala, et al.
Annals of Clinical Biochemistry
|
September 1, 1992
Comparison of post-mortem urinary and vitreous humour organic acids
M J Bennett, M C Ragni, I Hood, et al.
Page
of 9