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C A Stanley

Showing results (31-40 of 106) with videos related to

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Clinical Pediatrics|August 1, 1983
The effect of early feeding on plasma glucose levels in SGA infantsL L Wright, C A Stanley, E K Anday, et al.
The Journal of Pediatrics|April 1, 1981
Plasma ketones in newborn infants: absence of suckling ketosisE K Anday, C A Stanley, L Baker, et al.
American Heart Journal|January 29, 2000
Familial carnitine transporter defect: A treatable cause of cardiomyopathy in childrenM E Pierpont, G N Breningstall, C A Stanley, et al.
Pediatrics|November 1, 1979
Metabolic fuel and hormone responses to fasting in newborn infantsC A Stanley, E K Anday, L Baker, et al.
The Journal of Pediatrics|August 1, 1997
Mitochondrial carnitine-acylcarnitine translocase deficiency presenting as sudden neonatal deathR A Chalmers, C A Stanley, N English, et al.
The New England Journal of Medicine|March 15, 1979
Effect of tri-iodothyronine replacement on the metabolic and pituitary responses to starvationD F Gardner, M M Kaplan, C A Stanley, 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.
The Journal of Pediatrics|October 1, 1984
Systemic carnitine deficiency simulating Reye syndromeP M Coates, D E Hale, C A Stanley, et al.
Pageof 11

Showing results (31-40 of 106) with videos related to

Sort By:
Pageof 11
Clinical Pediatrics|August 1, 1983
The effect of early feeding on plasma glucose levels in SGA infantsL L Wright, C A Stanley, E K Anday, et al.
The Journal of Pediatrics|April 1, 1981
Plasma ketones in newborn infants: absence of suckling ketosisE K Anday, C A Stanley, L Baker, et al.
American Heart Journal|January 29, 2000
Familial carnitine transporter defect: A treatable cause of cardiomyopathy in childrenM E Pierpont, G N Breningstall, C A Stanley, et al.
Pediatrics|November 1, 1979
Metabolic fuel and hormone responses to fasting in newborn infantsC A Stanley, E K Anday, L Baker, et al.
The Journal of Pediatrics|August 1, 1997
Mitochondrial carnitine-acylcarnitine translocase deficiency presenting as sudden neonatal deathR A Chalmers, C A Stanley, N English, et al.
The New England Journal of Medicine|March 15, 1979
Effect of tri-iodothyronine replacement on the metabolic and pituitary responses to starvationD F Gardner, M M Kaplan, C A Stanley, 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.
The Journal of Pediatrics|October 1, 1984
Systemic carnitine deficiency simulating Reye syndromeP M Coates, D E Hale, C A Stanley, et al.
Pageof 11