Population newborn screening for inherited metabolic disease: Current UK perspectives

This publication has 25 references indexed in Scilit:

• Neonatal screening for cystic fibrosis
  BMJ, 1998
• Newborn screening for Duchenne muscular dystrophy
  Seminars in Neonatology, 1998
• Nutritional Benefits of Neonatal Screening for Cystic Fibrosis
  New England Journal of Medicine, 1997
• Why “underpowered” trials are not necessarily unethical
  The Lancet, 1997
• Delay in diagnosis of homocystinuria: retrospective study of consecutive patients
  BMJ, 1996
• Clinical trials and rare diseases: a way out of a conundrum
  BMJ, 1995
• Screening in infancy.
  Archives of Disease in Childhood, 1995
• The analysis of diagnostic markers of genetic disorders in human blood and urine using tandem mass spectrometry with liquid secondary ion mass spectrometry
  International Journal of Mass Spectrometry and Ion Processes, 1991
• Neonatal screening for cystic fibrosis in Wales and the West Midlands: clinical assessment after five years of screening.
  Archives of Disease in Childhood, 1991
• Incidence of congenital hypothyroidism: retrospective study of neonatal laboratory screening versus clinical symptoms as indicators leading to diagnosis.
  BMJ, 1984