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T Clayton

Showing results (51-60 of 248) with videos related to

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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.
BMJ Case Reports|May 17, 2015
A preterm neonate with seizures unresponsive to conventional treatmentFrancesco Raimondi, Philippa Mills, Peter T Clayton, et al.
British Journal of Anaesthesia|October 28, 1999
Gastric pressure during emergency caesarean section under general anaesthesiaE L Hartsilver, R G Vanner, J Bewley, et al.
European Journal of Pediatrics|March 21, 2003
Mitochondrial HMG-CoA synthase deficiency: identification of two further patients carrying two novel mutationsNicole I Wolf, Shamima Rahman, Peter T Clayton, 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.
Developmental Medicine and Child Neurology|September 25, 2012
Inborn errors of metabolism causing epilepsyShamima Rahman, Emma J Footitt, Sophia Varadkar, et al.
Pageof 25

Showing results (51-60 of 248) with videos related to

Sort By:
Pageof 25
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.
BMJ Case Reports|May 17, 2015
A preterm neonate with seizures unresponsive to conventional treatmentFrancesco Raimondi, Philippa Mills, Peter T Clayton, et al.
British Journal of Anaesthesia|October 28, 1999
Gastric pressure during emergency caesarean section under general anaesthesiaE L Hartsilver, R G Vanner, J Bewley, et al.
European Journal of Pediatrics|March 21, 2003
Mitochondrial HMG-CoA synthase deficiency: identification of two further patients carrying two novel mutationsNicole I Wolf, Shamima Rahman, Peter T Clayton, 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.
Developmental Medicine and Child Neurology|September 25, 2012
Inborn errors of metabolism causing epilepsyShamima Rahman, Emma J Footitt, Sophia Varadkar, et al.
Pageof 25