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K H Carpenter

Showing results (1-10 of 19) with videos related to

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Bulletin of the Medical Library Association|April 1, 1992
Evaluating library resources for accreditation: results of a studyK H Carpenter
AORN Journal|May 21, 1998
Developing a pediatric patient/parent hospital preparation programK H Carpenter
Journal of Inherited Metabolic Disease|October 13, 1999
Neonatal diagnosis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and implications for newborn screening by tandem mass spectrometryK H Carpenter, B Wilcken
Annals of Clinical Biochemistry|March 1, 1984
Experience with a simple high-performance liquid chromatography method for the analysis of purine and pyrimidine nucleosides and bases in biological fluidsM J Bennett, K H Carpenter
Archives of Disease in Childhood|September 1, 1993
Neonatal symptoms in medium chain acyl coenzyme A dehydrogenase deficiencyB Wilcken, K H Carpenter, J Hammond
Journal of Inherited Metabolic Disease|January 1, 1990
Rett's syndrome and ornithine carbamoyltransferase deficiencyK H Carpenter, J R Bonham, A Clarke
Clinical Chemistry|March 1, 1985
Asymptomatic xanthinuria detected as a result of routine analysis of serum for urateM J Bennett, K H Carpenter, P G Hill
Journal of Clinical Pathology|July 1, 1993
Vitreous humour and cerebrospinal fluid hypoxanthine concentration as a marker of pre-mortem hypoxia in SIDSK H Carpenter, J R Bonham, E Worthy, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Benign persistent orotic aciduria and the possibility of misdiagnosis of ornithine carbamoyltransferase deficiencyK H Carpenter, M Potter, J W Hammond, et al.
Clinical Chemistry|May 1, 1984
Cyclosporin concentrations in whole blood and plasmaM J Bennett, K H Carpenter, E Worthy, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Bulletin of the Medical Library Association|April 1, 1992
Evaluating library resources for accreditation: results of a studyK H Carpenter
AORN Journal|May 21, 1998
Developing a pediatric patient/parent hospital preparation programK H Carpenter
Journal of Inherited Metabolic Disease|October 13, 1999
Neonatal diagnosis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and implications for newborn screening by tandem mass spectrometryK H Carpenter, B Wilcken
Annals of Clinical Biochemistry|March 1, 1984
Experience with a simple high-performance liquid chromatography method for the analysis of purine and pyrimidine nucleosides and bases in biological fluidsM J Bennett, K H Carpenter
Archives of Disease in Childhood|September 1, 1993
Neonatal symptoms in medium chain acyl coenzyme A dehydrogenase deficiencyB Wilcken, K H Carpenter, J Hammond
Journal of Inherited Metabolic Disease|January 1, 1990
Rett's syndrome and ornithine carbamoyltransferase deficiencyK H Carpenter, J R Bonham, A Clarke
Clinical Chemistry|March 1, 1985
Asymptomatic xanthinuria detected as a result of routine analysis of serum for urateM J Bennett, K H Carpenter, P G Hill
Journal of Clinical Pathology|July 1, 1993
Vitreous humour and cerebrospinal fluid hypoxanthine concentration as a marker of pre-mortem hypoxia in SIDSK H Carpenter, J R Bonham, E Worthy, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Benign persistent orotic aciduria and the possibility of misdiagnosis of ornithine carbamoyltransferase deficiencyK H Carpenter, M Potter, J W Hammond, et al.
Clinical Chemistry|May 1, 1984
Cyclosporin concentrations in whole blood and plasmaM J Bennett, K H Carpenter, E Worthy, et al.
Pageof 2