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R J Pollitt

Showing results (71-80 of 133) with videos related to

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The British Journal of Ophthalmology|April 1, 1970
An unusual case of homocystinuriaJ B Garston, R R Gordon, C T Hart, et al.
The Journal of Physiology|April 1, 1972
The metabolite formed during choline transfer by the intestineR J Flower, R J Pollitt, P A Sanford, et al.
Pediatric Research|November 1, 1976
Ornithine transcarbamylase deficiency: enzyme studies on a further case and a method of diagnosis using plasma enzyme ratiosR G Gray, J A Black, V H Lyons, et al.
The Journal of Physiology|October 1, 1972
Metabolism and transfer of choline in hamster small intestineR J Flower, R J Pollitt, P A Sanford, et al.
Journal of Medical Screening|January 1, 1997
Neonatal screening for cystic fibrosis in the Trent region (UK): two-stage immunoreactive trypsin screening compared with a three-stage protocol with DNA analysis as an intermediate stepR J Pollitt, A Dalton, S Evans, et al.
Journal of Medical Genetics|September 2, 2000
Many deltaF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTR mutationJ Boyne, S Evans, R J Pollitt, et al.
Annals of Clinical Biochemistry|May 1, 1977
Enzyme studies on a new case of ornithine carbamoyl transferase deficiency: remaining problems and a method of diagnosis based on plasma enzyme ratiosR J Pollitt, J A Black, R G Gray, et al.
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, 1989
Generalised dicarboxylic aciduria: a common finding in neonatesM Downing, P Rose, M J Bennett, et al.
Journal of Inherited Metabolic Disease|January 1, 1983
A case of beta-ketothiolase deficiencyM J Bennett, J M Littlewood, A MacDonald, et al.
Pageof 14

Showing results (71-80 of 133) with videos related to

Sort By:
Pageof 14
The British Journal of Ophthalmology|April 1, 1970
An unusual case of homocystinuriaJ B Garston, R R Gordon, C T Hart, et al.
The Journal of Physiology|April 1, 1972
The metabolite formed during choline transfer by the intestineR J Flower, R J Pollitt, P A Sanford, et al.
Pediatric Research|November 1, 1976
Ornithine transcarbamylase deficiency: enzyme studies on a further case and a method of diagnosis using plasma enzyme ratiosR G Gray, J A Black, V H Lyons, et al.
The Journal of Physiology|October 1, 1972
Metabolism and transfer of choline in hamster small intestineR J Flower, R J Pollitt, P A Sanford, et al.
Journal of Medical Screening|January 1, 1997
Neonatal screening for cystic fibrosis in the Trent region (UK): two-stage immunoreactive trypsin screening compared with a three-stage protocol with DNA analysis as an intermediate stepR J Pollitt, A Dalton, S Evans, et al.
Journal of Medical Genetics|September 2, 2000
Many deltaF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTR mutationJ Boyne, S Evans, R J Pollitt, et al.
Annals of Clinical Biochemistry|May 1, 1977
Enzyme studies on a new case of ornithine carbamoyl transferase deficiency: remaining problems and a method of diagnosis based on plasma enzyme ratiosR J Pollitt, J A Black, R G Gray, et al.
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, 1989
Generalised dicarboxylic aciduria: a common finding in neonatesM Downing, P Rose, M J Bennett, et al.
Journal of Inherited Metabolic Disease|January 1, 1983
A case of beta-ketothiolase deficiencyM J Bennett, J M Littlewood, A MacDonald, et al.
Pageof 14