Search research articles
Contact Us
Filters
Showing results (61-70 of 133) with videos related to
Page
of 14
Sort By:
Journal of Chromatography
|
June 10, 1992
Identification of urinary acylcarnitines using gas chromatography-mass spectrometry: preliminary clinical applications
S 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 illness
E M Layward, M S Tanner, R J Pollitt, et al.
Lancet (London, England)
|
June 24, 1989
Pyroglutamicaciduria from vigabatrin
J 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 fibroblasts
N 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 findings
M 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 death
M 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 system
H 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 baby
P 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 oxidation
R J Pollitt, N J Manning, S E Olpin, et al.
Page
of 14
Search research articles
Search
Showing results (61-70 of 133) with videos related to
Sort By:
Page
of 14
Journal of Chromatography
|
June 10, 1992
Identification of urinary acylcarnitines using gas chromatography-mass spectrometry: preliminary clinical applications
S 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 illness
E M Layward, M S Tanner, R J Pollitt, et al.
Lancet (London, England)
|
June 24, 1989
Pyroglutamicaciduria from vigabatrin
J 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 fibroblasts
N 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 findings
M 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 death
M 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 system
H 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 baby
P 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 oxidation
R J Pollitt, N J Manning, S E Olpin, et al.
Page
of 14