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Acta Paediatrica (Oslo, Norway : 1992)
|
July 22, 2010
New technologies extend the scope of newborn blood-spot screening, but old problems remain unresolved
Rodney 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
Journal of Medical Biochemistry
|
March 31, 2017
Different Viewpoints: International Perspectives on Newborn Screening
Rodney J Pollitt
Journal of Inherited Metabolic Disease
|
July 10, 2007
Introducing new screens: why are we all doing different things?
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
|
June 15, 1979
The occurrence of gamma-glutamylphenylalanine in the urine of newborn phenylketonurics
H Peck, R J Pollitt
Journal of Inherited Metabolic Disease
|
July 17, 1999
Population newborn screening for inherited metabolic disease: current UK perspectives
A Green, R J Pollitt
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 1, 1978
3-Aminopiperid-2-one, an unusual metabolite in the urine of a patient with hyperammonaemia, hyperornithinaemia and homocitrullinuria
V Fell, R J Pollitt
Journal of Inherited Metabolic Disease
|
January 1, 1980
Ascorbic acid: an unstable ninhydrin-positive urinary constituent running with valine in a commonly used screening system
R J Pollitt, B Sandhu
Journal of Health Care Chaplaincy
|
January 9, 2015
Delivering chaplaincy services to veterans at increased risk of suicide
Marek S Kopacz, Michael J Pollitt
Page
of 10
Search research articles
Search
Showing results (11-20 of 95) with videos related to
Sort By:
Page
of 10
Acta Paediatrica (Oslo, Norway : 1992)
|
July 22, 2010
New technologies extend the scope of newborn blood-spot screening, but old problems remain unresolved
Rodney 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
Journal of Medical Biochemistry
|
March 31, 2017
Different Viewpoints: International Perspectives on Newborn Screening
Rodney J Pollitt
Journal of Inherited Metabolic Disease
|
July 10, 2007
Introducing new screens: why are we all doing different things?
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
|
June 15, 1979
The occurrence of gamma-glutamylphenylalanine in the urine of newborn phenylketonurics
H Peck, R J Pollitt
Journal of Inherited Metabolic Disease
|
July 17, 1999
Population newborn screening for inherited metabolic disease: current UK perspectives
A Green, R J Pollitt
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 1, 1978
3-Aminopiperid-2-one, an unusual metabolite in the urine of a patient with hyperammonaemia, hyperornithinaemia and homocitrullinuria
V Fell, R J Pollitt
Journal of Inherited Metabolic Disease
|
January 1, 1980
Ascorbic acid: an unstable ninhydrin-positive urinary constituent running with valine in a commonly used screening system
R J Pollitt, B Sandhu
Journal of Health Care Chaplaincy
|
January 9, 2015
Delivering chaplaincy services to veterans at increased risk of suicide
Marek S Kopacz, Michael J Pollitt
Page
of 10