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R J Pollitt

Showing results (91-100 of 133) with videos related to

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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.
Journal of Inherited Metabolic Disease|January 1, 1991
Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorderM J Bennett, R J Pollitt, S I Goodman, et al.
The British Journal of Psychiatry : the Journal of Mental Science|December 1, 1975
The relationship of plasma to erythrocyte lithium levels in patients taking lithium carbonateC R Lee, S E Hill, M Dimitrakoudi, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
The diagnosis and biochemical investigation of a patient with a short chain fatty acid oxidation defectM J Bennett, R G Gray, D M Isherwood, et al.
Progress in Clinical and Biological Research|January 1, 1992
Medium chain acyl-CoA dehydrogenase deficiency in the United KingdomD Curtis, A I Blakemore, P C Engel, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Lethal multiple acyl-CoA dehydrogenation deficiency with dysmorphic featuresM J Bennett, R J Pollitt, J M Land, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Primary hyperoxaluria and L-glyceric aciduria in the catW F Blakemore, M F Heath, M J Bennett, et al.
Acta Paediatrica Scandinavica|July 1, 1977
Carbamyl-phosphate-synthetase deficiency with neonatal onset of symptomsJ P Farriaux, C Ponte, R J Pollitt, et al.
Advances in Experimental Medicine and Biology|March 10, 2000
The use of [9,10-3H]myristate, [9,10-3H]palmitate and [9,10-3H]oleate for the detection and diagnosis of medium and long-chain fatty acid oxidation disorders in intact cultured fibroblastsS E Olpin, N J Manning, R J Pollitt, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Neonatal screening for dihydropteridine reductase deficiencyA Sahota, J A Blair, P A Barford, et al.
Pageof 14

Showing results (91-100 of 133) with videos related to

Sort By:
Pageof 14
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.
Journal of Inherited Metabolic Disease|January 1, 1991
Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorderM J Bennett, R J Pollitt, S I Goodman, et al.
The British Journal of Psychiatry : the Journal of Mental Science|December 1, 1975
The relationship of plasma to erythrocyte lithium levels in patients taking lithium carbonateC R Lee, S E Hill, M Dimitrakoudi, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
The diagnosis and biochemical investigation of a patient with a short chain fatty acid oxidation defectM J Bennett, R G Gray, D M Isherwood, et al.
Progress in Clinical and Biological Research|January 1, 1992
Medium chain acyl-CoA dehydrogenase deficiency in the United KingdomD Curtis, A I Blakemore, P C Engel, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Lethal multiple acyl-CoA dehydrogenation deficiency with dysmorphic featuresM J Bennett, R J Pollitt, J M Land, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Primary hyperoxaluria and L-glyceric aciduria in the catW F Blakemore, M F Heath, M J Bennett, et al.
Acta Paediatrica Scandinavica|July 1, 1977
Carbamyl-phosphate-synthetase deficiency with neonatal onset of symptomsJ P Farriaux, C Ponte, R J Pollitt, et al.
Advances in Experimental Medicine and Biology|March 10, 2000
The use of [9,10-3H]myristate, [9,10-3H]palmitate and [9,10-3H]oleate for the detection and diagnosis of medium and long-chain fatty acid oxidation disorders in intact cultured fibroblastsS E Olpin, N J Manning, R J Pollitt, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Neonatal screening for dihydropteridine reductase deficiencyA Sahota, J A Blair, P A Barford, et al.
Pageof 14