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R J Pollitt

Showing results (51-60 of 133) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1983
Studies on the pathway from ornithine to proline in cultured skin fibroblasts with reference to the defect in hyperornithinaemia with hyperammonaemia and homocitrullinuriaR G Gray, S E Hill, R J Pollitt
Clinical Science and Molecular Medicine|June 1, 1974
The relationship between the formation of urea and argininosuccinate in a patient with argininosuccinic aciduria studied with labelled precursorsC W Crane, F A Jenner, R J Pollitt
Journal of Medical Genetics|March 1, 1988
Family size limitation: a method for demonstrating recessive inheritanceJ F Brookfield, R J Pollitt, I D Young
BMJ (Clinical Research Ed.)|September 16, 1995
Survey of scope of neonatal screening in the United KingdomA Streetly, C Grant, R J Pollitt, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Acquired deficiency of long-chain acyl-CoA dehydrogenase in liver: a cautionary taleF Allison, M J Bennett, R J Pollitt, et al.
Annals of Clinical Biochemistry|January 1, 1984
The routine investigation of urinary organic acids in selected paediatric patients: results over a 2 1/2-year periodM J Bennett, A Green, R J Pollitt, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 17, 1973
Glycoasparagine metabolites in patients with aspartylglycosaminuria: comparison between English and Finnish patients with special reference to storage materialsJ Palo, R J Pollitt, K M Pretty, et al.
Progress in Clinical and Biological Research|January 1, 1990
Fatty acid oxidation defects as causes of unexpected death in infancyM J Bennett, F Allison, R J Pollitt, et al.
American Journal of Diseases of Children (1960)|May 1, 1974
Ornithinemia, hyperammonemia, and homocitrullinuria. A disease associated with mental retardation and possibly caused by defective mitochondrial transportV Fell, R J Pollitt, G A Sampson, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Improved detection of long-chain fatty acid oxidation defects in intact cells using [9,10-3H]oleic acidS E Olpin, N J Manning, R J Pollitt, et al.
Pageof 14

Showing results (51-60 of 133) with videos related to

Sort By:
Pageof 14
Journal of Inherited Metabolic Disease|January 1, 1983
Studies on the pathway from ornithine to proline in cultured skin fibroblasts with reference to the defect in hyperornithinaemia with hyperammonaemia and homocitrullinuriaR G Gray, S E Hill, R J Pollitt
Clinical Science and Molecular Medicine|June 1, 1974
The relationship between the formation of urea and argininosuccinate in a patient with argininosuccinic aciduria studied with labelled precursorsC W Crane, F A Jenner, R J Pollitt
Journal of Medical Genetics|March 1, 1988
Family size limitation: a method for demonstrating recessive inheritanceJ F Brookfield, R J Pollitt, I D Young
BMJ (Clinical Research Ed.)|September 16, 1995
Survey of scope of neonatal screening in the United KingdomA Streetly, C Grant, R J Pollitt, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Acquired deficiency of long-chain acyl-CoA dehydrogenase in liver: a cautionary taleF Allison, M J Bennett, R J Pollitt, et al.
Annals of Clinical Biochemistry|January 1, 1984
The routine investigation of urinary organic acids in selected paediatric patients: results over a 2 1/2-year periodM J Bennett, A Green, R J Pollitt, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 17, 1973
Glycoasparagine metabolites in patients with aspartylglycosaminuria: comparison between English and Finnish patients with special reference to storage materialsJ Palo, R J Pollitt, K M Pretty, et al.
Progress in Clinical and Biological Research|January 1, 1990
Fatty acid oxidation defects as causes of unexpected death in infancyM J Bennett, F Allison, R J Pollitt, et al.
American Journal of Diseases of Children (1960)|May 1, 1974
Ornithinemia, hyperammonemia, and homocitrullinuria. A disease associated with mental retardation and possibly caused by defective mitochondrial transportV Fell, R J Pollitt, G A Sampson, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Improved detection of long-chain fatty acid oxidation defects in intact cells using [9,10-3H]oleic acidS E Olpin, N J Manning, R J Pollitt, et al.
Pageof 14