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P T Clayton

Showing results (21-30 of 101) with videos related to

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Archives of Biochemistry and Biophysics|October 6, 2000
A new method for the analysis of urinary vitamin E metabolites and the tentative identification of a novel group of compoundsS A Pope, P T Clayton, D P Muller
Archives of Disease in Childhood|July 1, 1997
Pearson's syndrome without marrow involvementA A Morris, P J Lamont, P T Clayton
Journal of the Royal Society of Medicine|December 1, 1996
Idiopathic rhabdomyolysisJ Fraser, S Fang, R Barfoot, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 19, 2000
Effect of intravenous lipid emulsions on hepatic cholesterol metabolismP D Whitfield, P T Clayton, D P Muller
Journal of the American Academy of Dermatology|August 1, 1989
X-linked dominant Conradi-Hünermann syndrome presenting as congenital erythrodermaD C Kalter, D J Atherton, P T Clayton
Journal of Inherited Metabolic Disease|January 1, 1986
3-Hydroxy-3-methylglutaryl-CoA lyase deficiencyJ H Walter, P T Clayton, J V Leonard
European Journal of Pediatrics|January 1, 1991
Mitochondrial phosphoenolpyruvate carboxykinase deficiencyJ V Leonard, K Hyland, N Furukawa, et al.
European Journal of Pediatrics|April 1, 1986
Mitochondrial phosphoenolpyruvate carboxykinase deficiencyP T Clayton, K Hyland, M Brand, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1985
Impaired neurotransmitter amine metabolism in arginase deficiencyK Hyland, I Smith, P T Clayton, et al.
Neurology|October 1, 1992
Aromatic L-amino acid decarboxylase deficiency: clinical features, diagnosis, and treatment of a new inborn error of neurotransmitter amine synthesisK Hyland, R A Surtees, C Rodeck, et al.
Pageof 11

Showing results (21-30 of 101) with videos related to

Sort By:
Pageof 11
Archives of Biochemistry and Biophysics|October 6, 2000
A new method for the analysis of urinary vitamin E metabolites and the tentative identification of a novel group of compoundsS A Pope, P T Clayton, D P Muller
Archives of Disease in Childhood|July 1, 1997
Pearson's syndrome without marrow involvementA A Morris, P J Lamont, P T Clayton
Journal of the Royal Society of Medicine|December 1, 1996
Idiopathic rhabdomyolysisJ Fraser, S Fang, R Barfoot, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 19, 2000
Effect of intravenous lipid emulsions on hepatic cholesterol metabolismP D Whitfield, P T Clayton, D P Muller
Journal of the American Academy of Dermatology|August 1, 1989
X-linked dominant Conradi-Hünermann syndrome presenting as congenital erythrodermaD C Kalter, D J Atherton, P T Clayton
Journal of Inherited Metabolic Disease|January 1, 1986
3-Hydroxy-3-methylglutaryl-CoA lyase deficiencyJ H Walter, P T Clayton, J V Leonard
European Journal of Pediatrics|January 1, 1991
Mitochondrial phosphoenolpyruvate carboxykinase deficiencyJ V Leonard, K Hyland, N Furukawa, et al.
European Journal of Pediatrics|April 1, 1986
Mitochondrial phosphoenolpyruvate carboxykinase deficiencyP T Clayton, K Hyland, M Brand, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1985
Impaired neurotransmitter amine metabolism in arginase deficiencyK Hyland, I Smith, P T Clayton, et al.
Neurology|October 1, 1992
Aromatic L-amino acid decarboxylase deficiency: clinical features, diagnosis, and treatment of a new inborn error of neurotransmitter amine synthesisK Hyland, R A Surtees, C Rodeck, et al.
Pageof 11