Data required for the evaluation of newborn screening programmes

This publication has 23 references indexed in Scilit:

• Tandem mass spectrometric analysis for amino, organic, and fatty acid disorders in newborn dried blood spots: a two-year summary from the New England Newborn Screening Program.
  2001
• Neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency
  The Lancet, 2001
• Evaluation of newborn screening for medium chain acyl-CoA dehydrogenase deficiency in 275 000 babies
  Archives of Disease in Childhood: Fetal & Neonatal, 2001
• Evaluating newborn screening programmes based on dried blood spots: future challenges.
  British Medical Bulletin, 1998
• Neonatal screening for inborn errors of metabolism: cost, yield and outcome.
  Health Technology Assessment, 1997
• Morbidity and mortality in medium chain acyl coenzyme A dehydrogenase deficiency.
  Archives of Disease in Childhood, 1994
• Medium–chain acyl-coenzyme A dehydrogenase deficiency: Clinical course in 120 affected children
  The Journal of Pediatrics, 1994
• Neonatal symptoms in medium chain acyl coenzyme A dehydrogenase deficiency.
  Archives of Disease in Childhood, 1993
• Sudden Infant Death Syndrome and Inherited Disorders of Fatty Acid β-Oxidation
  Neonatology, 1990
• Parental rights, child welfare, and public health: the case of PKU screening.
  American Journal of Public Health, 1982