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J Pollitt

Showing results (51-60 of 95) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1987
Urinary organic acids in succinic semialdehyde dehydrogenase deficiency: evidence of alpha-oxidation of 4-hydroxybutyric acid, interaction of succinic semialdehyde with pyruvate dehydrogenase and possible secondary inhibition of mitochondrial beta-oxidationG K Brown, C H Cromby, N J Manning, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Differential diagnosis of hydroxydicarboxylic aciduria based on release of 3H2O from [9,10-3H]myristic and [9,10-3H]palmitic acids by intact cultured fibroblastsS E Olpin, N J Manning, K Carpenter, et al.
The British Journal of Surgery|July 19, 2017
Operative learning curve trajectory in a cohort of surgical traineesC Brown, T Abdelrahman, N Patel, et al.
Archives of Disease in Childhood|March 1, 1982
Unexplained diarrhoea and failure to thrive in 2 siblings with unusual facies and abnormal scalp hair shafts: a new syndromeL Stankler, D Lloyd, R J Pollitt, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Riboflavin-responsive ethylmalonic-adipic aciduriaA Green, T G Marshall, M J Bennett, et al.
Journal of Inherited Metabolic Disease|August 18, 2000
Molecular characterization of methylmalonate semialdehyde dehydrogenase deficiencyK L Chambliss, R G Gray, G Rylance, et al.
The Biochemical Journal|March 1, 1980
The use of arginine analogues for investigating the functional organization of the arginine-binding site in lobster muscle arginine kinase. Role of the 'essential' thiol groupD C Watts, E O Anosike, B Moreland, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 16, 1987
Increased excretion of propan-1,3-diol and 3-hydroxypropionic acid apparently caused by abnormal bacterial metabolism in the gutR J Pollitt, B Fowler, I B Sardharwalla, et al.
Clinical Cardiology|March 1, 1996
Endocardial fibroelastosis and primary carnitine deficiency due to a defect in the plasma membrane carnitine transporterM J Bennett, D E Hale, R J Pollitt, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
6-Methyluracil excretion in 2-methylacetoacetyl-CoA thiolase deficiency and in two children with an unexplained recurrent ketoacidaemiaC H Cromby, N J Manning, R J Pollitt, et al.
Pageof 10

Showing results (51-60 of 95) with videos related to

Sort By:
Pageof 10
Journal of Inherited Metabolic Disease|January 1, 1987
Urinary organic acids in succinic semialdehyde dehydrogenase deficiency: evidence of alpha-oxidation of 4-hydroxybutyric acid, interaction of succinic semialdehyde with pyruvate dehydrogenase and possible secondary inhibition of mitochondrial beta-oxidationG K Brown, C H Cromby, N J Manning, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Differential diagnosis of hydroxydicarboxylic aciduria based on release of 3H2O from [9,10-3H]myristic and [9,10-3H]palmitic acids by intact cultured fibroblastsS E Olpin, N J Manning, K Carpenter, et al.
The British Journal of Surgery|July 19, 2017
Operative learning curve trajectory in a cohort of surgical traineesC Brown, T Abdelrahman, N Patel, et al.
Archives of Disease in Childhood|March 1, 1982
Unexplained diarrhoea and failure to thrive in 2 siblings with unusual facies and abnormal scalp hair shafts: a new syndromeL Stankler, D Lloyd, R J Pollitt, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Riboflavin-responsive ethylmalonic-adipic aciduriaA Green, T G Marshall, M J Bennett, et al.
Journal of Inherited Metabolic Disease|August 18, 2000
Molecular characterization of methylmalonate semialdehyde dehydrogenase deficiencyK L Chambliss, R G Gray, G Rylance, et al.
The Biochemical Journal|March 1, 1980
The use of arginine analogues for investigating the functional organization of the arginine-binding site in lobster muscle arginine kinase. Role of the 'essential' thiol groupD C Watts, E O Anosike, B Moreland, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 16, 1987
Increased excretion of propan-1,3-diol and 3-hydroxypropionic acid apparently caused by abnormal bacterial metabolism in the gutR J Pollitt, B Fowler, I B Sardharwalla, et al.
Clinical Cardiology|March 1, 1996
Endocardial fibroelastosis and primary carnitine deficiency due to a defect in the plasma membrane carnitine transporterM J Bennett, D E Hale, R J Pollitt, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
6-Methyluracil excretion in 2-methylacetoacetyl-CoA thiolase deficiency and in two children with an unexplained recurrent ketoacidaemiaC H Cromby, N J Manning, R J Pollitt, et al.
Pageof 10