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D E HALE

Showing results (21-30 of 85) with videos related to

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The Journal of Pediatrics|January 1, 1995
Transient organic aciduria and persistent lacticacidemia in a patient with short-chain acyl-coenzyme A dehydrogenase deficiencyD B Dawson, L Waber, D E Hale, 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.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1992
Identification of urinary metabolites of (+/-)-2-(p-isobutylphenyl)propionic acid (Ibuprofen) by routine organic acid screeningM J Bennett, W G Sherwood, A Bhala, et al.
The Journal of Pediatrics|January 1, 1993
Limitations of 3-phenylpropionylglycine in early screening for medium-chain acyl-coenzyme A dehydrogenase deficiencyA Bhala, M J Bennett, K L McGowan, et al.
Biochemical and Molecular Medicine|June 1, 1995
Long-chain acyl-CoA profiles in cultured fibroblasts from patients with defects in fatty acid oxidationC S Tamvakopoulos, S Willi, V E Anderson, et al.
Pediatric Neurology|January 1, 1995
Clinical and neurophysiologic response of myopathy and neuropathy in long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency to oral prednisoneI Tein, E J Donner, D E Hale, et al.
Diabetes Care|October 20, 1999
A quantitative scale of acanthosis nigricansJ P Burke, D E Hale, H P Hazuda, et al.
Pediatric Pathology|May 1, 1991
Postmortem recognition of fatty acid oxidation disordersM J Bennett, D E Hale, P M Coates, et al.
Progress in Clinical and Biological Research|January 1, 1990
A genetic defect in carnitine transport causing primary carnitine deficiencyC A Stanley, W R Treem, D E Hale, et al.
American Journal of Diseases of Children (1960)|April 1, 1986
Metabolic disorder possible cause of Reye's syndromeR I Kelley, P M Coates, D E Hale, et al.
Pageof 9

Showing results (21-30 of 85) with videos related to

Sort By:
Pageof 9
The Journal of Pediatrics|January 1, 1995
Transient organic aciduria and persistent lacticacidemia in a patient with short-chain acyl-coenzyme A dehydrogenase deficiencyD B Dawson, L Waber, D E Hale, 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.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1992
Identification of urinary metabolites of (+/-)-2-(p-isobutylphenyl)propionic acid (Ibuprofen) by routine organic acid screeningM J Bennett, W G Sherwood, A Bhala, et al.
The Journal of Pediatrics|January 1, 1993
Limitations of 3-phenylpropionylglycine in early screening for medium-chain acyl-coenzyme A dehydrogenase deficiencyA Bhala, M J Bennett, K L McGowan, et al.
Biochemical and Molecular Medicine|June 1, 1995
Long-chain acyl-CoA profiles in cultured fibroblasts from patients with defects in fatty acid oxidationC S Tamvakopoulos, S Willi, V E Anderson, et al.
Pediatric Neurology|January 1, 1995
Clinical and neurophysiologic response of myopathy and neuropathy in long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency to oral prednisoneI Tein, E J Donner, D E Hale, et al.
Diabetes Care|October 20, 1999
A quantitative scale of acanthosis nigricansJ P Burke, D E Hale, H P Hazuda, et al.
Pediatric Pathology|May 1, 1991
Postmortem recognition of fatty acid oxidation disordersM J Bennett, D E Hale, P M Coates, et al.
Progress in Clinical and Biological Research|January 1, 1990
A genetic defect in carnitine transport causing primary carnitine deficiencyC A Stanley, W R Treem, D E Hale, et al.
American Journal of Diseases of Children (1960)|April 1, 1986
Metabolic disorder possible cause of Reye's syndromeR I Kelley, P M Coates, D E Hale, et al.
Pageof 9