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Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
January 8, 2000
Principles and performance: assessing the evidence
R J Pollitt
Journal of Inherited Metabolic Disease
|
June 19, 2001
Newborn mass screening versus selective investigation: benefits and costs
R J Pollitt
Journal of Inherited Metabolic Disease
|
January 24, 2004
Newborn screening for cystic fibrosis: science, legislation, and human values
R 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 death
R J Pollitt
Progress in Clinical and Biological Research
|
January 1, 1990
Clinical and biochemical presentations in 20 cases of hydroxydicarboxylic aciduria
R J Pollitt
Journal of Clinical Pathology
|
June 1, 1993
Neonatal screening
R 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 acidemia
R 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 normals
R J Pollitt
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of 14
Search research articles
Search
Showing results (11-20 of 133) with videos related to
Sort By:
Page
of 14
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
January 8, 2000
Principles and performance: assessing the evidence
R J Pollitt
Journal of Inherited Metabolic Disease
|
June 19, 2001
Newborn mass screening versus selective investigation: benefits and costs
R J Pollitt
Journal of Inherited Metabolic Disease
|
January 24, 2004
Newborn screening for cystic fibrosis: science, legislation, and human values
R 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 death
R J Pollitt
Progress in Clinical and Biological Research
|
January 1, 1990
Clinical and biochemical presentations in 20 cases of hydroxydicarboxylic aciduria
R J Pollitt
Journal of Clinical Pathology
|
June 1, 1993
Neonatal screening
R 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 acidemia
R 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 normals
R J Pollitt
Page
of 14