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R J Pollitt

Showing results (11-20 of 133) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
Principles and performance: assessing the evidenceR J Pollitt
Journal of Inherited Metabolic Disease|June 19, 2001
Newborn mass screening versus selective investigation: benefits and costsR J Pollitt
Journal of Inherited Metabolic Disease|January 24, 2004
Newborn screening for cystic fibrosis: science, legislation, and human valuesR J Pollitt
Journal of Inherited Metabolic Disease|January 1, 1989
Disorders of mitochondrial beta-oxidation: prenatal and early postnatal diagnosis and their relevance to Reye's syndrome and sudden infant deathR J Pollitt
Progress in Clinical and Biological Research|January 1, 1990
Clinical and biochemical presentations in 20 cases of hydroxydicarboxylic aciduriaR J Pollitt
Journal of Clinical Pathology|June 1, 1993
Neonatal screeningR J Pollitt
Journal of Inherited Metabolic Disease|July 10, 2007
Introducing new screens: why are we all doing different things?R J Pollitt
The Journal of Pediatrics|September 1, 1987
Endogenous catabolism as source of toxic metabolites in isovaleric acidemiaR J Pollitt
Journal of Inherited Metabolic Disease|June 22, 2012
Commentary: What degree of hyperphenylalaninaemia requires treatment?R J Pollitt
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 30, 1974
Phenylpropionic acid in the urine of patients with phenylketonuria and normalsR J Pollitt
Pageof 14

Showing results (11-20 of 133) with videos related to

Sort By:
Pageof 14
Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
Principles and performance: assessing the evidenceR J Pollitt
Journal of Inherited Metabolic Disease|June 19, 2001
Newborn mass screening versus selective investigation: benefits and costsR J Pollitt
Journal of Inherited Metabolic Disease|January 24, 2004
Newborn screening for cystic fibrosis: science, legislation, and human valuesR J Pollitt
Journal of Inherited Metabolic Disease|January 1, 1989
Disorders of mitochondrial beta-oxidation: prenatal and early postnatal diagnosis and their relevance to Reye's syndrome and sudden infant deathR J Pollitt
Progress in Clinical and Biological Research|January 1, 1990
Clinical and biochemical presentations in 20 cases of hydroxydicarboxylic aciduriaR J Pollitt
Journal of Clinical Pathology|June 1, 1993
Neonatal screeningR J Pollitt
Journal of Inherited Metabolic Disease|July 10, 2007
Introducing new screens: why are we all doing different things?R J Pollitt
The Journal of Pediatrics|September 1, 1987
Endogenous catabolism as source of toxic metabolites in isovaleric acidemiaR J Pollitt
Journal of Inherited Metabolic Disease|June 22, 2012
Commentary: What degree of hyperphenylalaninaemia requires treatment?R J Pollitt
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 30, 1974
Phenylpropionic acid in the urine of patients with phenylketonuria and normalsR J Pollitt
Pageof 14