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R J Pollitt

Showing results (61-70 of 133) with videos related to

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Journal of Chromatography|June 10, 1992
Identification of urinary acylcarnitines using gas chromatography-mass spectrometry: preliminary clinical applicationsS Lowes, M E Rose, G A Mills, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency presenting as a Reye syndrome-like illnessE M Layward, M S Tanner, R J Pollitt, et al.
Lancet (London, England)|June 24, 1989
Pyroglutamicaciduria from vigabatrinJ R Bonham, J M Rattenbury, A Meeks, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
A comparison of [9,10-3H]palmitic and [9,10-3H]myristic acids for the detection of defects of fatty acid oxidation in intact cultured fibroblastsN J Manning, S E Olpin, R J Pollitt, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Possible deleterious effect of L-carnitine supplementation in a patient with mild multiple acyl-CoA dehydrogenation deficiency (ethylmalonic-adipic aciduria)A Green, M A Preece, C de Sousa, et al.
European Journal of Pediatrics|October 1, 1986
Glutaric aciduria type 1: biochemical investigations and postmortem findingsM J Bennett, N Marlow, R J Pollitt, et al.
Clinical Chemistry|September 1, 1990
Medium-chain acyl-CoA dehydrogenase deficiency: a useful diagnosis five years after deathM J Bennett, R J Pollitt, L S Taitz, et al.
Clinical Chemistry|March 1, 1997
Population screening for the common G985 mutation causing medium-chain acyl-CoA dehydrogenase deficiency with Eu-labeled oligonucleotides and the DELFIA systemH R Seddon, G Gray, R J Pollitt, et al.
Journal of Inherited Metabolic Disease|January 1, 1981
Hypermethioninaemia and 3-hydroxyisobutyric aciduria in an apparently healthy babyP J Congdon, D Haigh, R Smith, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Prenatal diagnosis of a defect in medium-chain fatty acid oxidationR J Pollitt, N J Manning, S E Olpin, et al.
Pageof 14

Showing results (61-70 of 133) with videos related to

Sort By:
Pageof 14
Journal of Chromatography|June 10, 1992
Identification of urinary acylcarnitines using gas chromatography-mass spectrometry: preliminary clinical applicationsS Lowes, M E Rose, G A Mills, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency presenting as a Reye syndrome-like illnessE M Layward, M S Tanner, R J Pollitt, et al.
Lancet (London, England)|June 24, 1989
Pyroglutamicaciduria from vigabatrinJ R Bonham, J M Rattenbury, A Meeks, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
A comparison of [9,10-3H]palmitic and [9,10-3H]myristic acids for the detection of defects of fatty acid oxidation in intact cultured fibroblastsN J Manning, S E Olpin, R J Pollitt, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Possible deleterious effect of L-carnitine supplementation in a patient with mild multiple acyl-CoA dehydrogenation deficiency (ethylmalonic-adipic aciduria)A Green, M A Preece, C de Sousa, et al.
European Journal of Pediatrics|October 1, 1986
Glutaric aciduria type 1: biochemical investigations and postmortem findingsM J Bennett, N Marlow, R J Pollitt, et al.
Clinical Chemistry|September 1, 1990
Medium-chain acyl-CoA dehydrogenase deficiency: a useful diagnosis five years after deathM J Bennett, R J Pollitt, L S Taitz, et al.
Clinical Chemistry|March 1, 1997
Population screening for the common G985 mutation causing medium-chain acyl-CoA dehydrogenase deficiency with Eu-labeled oligonucleotides and the DELFIA systemH R Seddon, G Gray, R J Pollitt, et al.
Journal of Inherited Metabolic Disease|January 1, 1981
Hypermethioninaemia and 3-hydroxyisobutyric aciduria in an apparently healthy babyP J Congdon, D Haigh, R Smith, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Prenatal diagnosis of a defect in medium-chain fatty acid oxidationR J Pollitt, N J Manning, S E Olpin, et al.
Pageof 14