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R J Pollitt

Showing results (1-10 of 133) with videos related to

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Lancet (London, England)|March 17, 1979
Investigation of atypical phenylketonuriaR J Pollitt
Journal of Inherited Metabolic Disease|May 5, 2009
Newborn blood spot screening: new opportunities, old problemsR J Pollitt
Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
Tandem mass spectrometry screening: proving effectivenessR J Pollitt
Padiatrie Und Padologie|January 1, 1993
Defects in mitochondrial fatty acid oxidation: clinical presentations and their role in sudden infant deathR J Pollitt
Journal of Inherited Metabolic Disease|January 1, 1983
Neonatal screening in FranceR J Pollitt
Biomedical Mass Spectrometry|April 1, 1983
The occurrence of substituted 3-methyl-3-hydroxyglutaric acids in urine in propionic acidaemia and in beta-ketothiolase deficiencyR J Pollitt
Journal of Inherited Metabolic Disease|June 10, 2006
International perspectives on newborn screeningR J Pollitt
Journal of Inherited Metabolic Disease|January 1, 1995
Disorders of mitochondrial long-chain fatty acid oxidationR J Pollitt
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 15, 1978
Loads versus tracers for assessing phenylalanine hydroxylase activity using plasma phenylalanine decay curvesR J Pollitt
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 14, 1973
Argininosuccinate lyase levels in blood, liver and cultured fibroblasts of a patient with argininosuccinic aciduriaR J Pollitt
Pageof 14

Showing results (1-10 of 133) with videos related to

Sort By:
Pageof 14
Lancet (London, England)|March 17, 1979
Investigation of atypical phenylketonuriaR J Pollitt
Journal of Inherited Metabolic Disease|May 5, 2009
Newborn blood spot screening: new opportunities, old problemsR J Pollitt
Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
Tandem mass spectrometry screening: proving effectivenessR J Pollitt
Padiatrie Und Padologie|January 1, 1993
Defects in mitochondrial fatty acid oxidation: clinical presentations and their role in sudden infant deathR J Pollitt
Journal of Inherited Metabolic Disease|January 1, 1983
Neonatal screening in FranceR J Pollitt
Biomedical Mass Spectrometry|April 1, 1983
The occurrence of substituted 3-methyl-3-hydroxyglutaric acids in urine in propionic acidaemia and in beta-ketothiolase deficiencyR J Pollitt
Journal of Inherited Metabolic Disease|June 10, 2006
International perspectives on newborn screeningR J Pollitt
Journal of Inherited Metabolic Disease|January 1, 1995
Disorders of mitochondrial long-chain fatty acid oxidationR J Pollitt
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 15, 1978
Loads versus tracers for assessing phenylalanine hydroxylase activity using plasma phenylalanine decay curvesR J Pollitt
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 14, 1973
Argininosuccinate lyase levels in blood, liver and cultured fibroblasts of a patient with argininosuccinic aciduriaR J Pollitt
Pageof 14