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J Pollitt

Showing results (1-10 of 95) with videos related to

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British Journal of Hospital Medicine|December 1, 1987
Monoamine oxidase inhibitors: have they a place, have they a future?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
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
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
Pageof 10

Showing results (1-10 of 95) with videos related to

Sort By:
Pageof 10
British Journal of Hospital Medicine|December 1, 1987
Monoamine oxidase inhibitors: have they a place, have they a future?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
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
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
Pageof 10