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  • Neonatal screening
  • Prenatal diagnostics
  • Congenital adrenal hyperplasia
  • Storage diseases
  • Galactosemia
  • Tyrosinemia
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    Citation
    11997Neonatal screening for inborn errors of metabolism: cost, yield and outcome.



    +-nlHealth Technol Assess 1(7):i-iv, 1-202 (1997)
    22004Neonatal screening for congenital adrenal hyperplasia.



    +-nlEur J Endocrinol 151 Suppl 3(-):U71-5 (2004)
    32010Newborn screening of lysosomal storage disorders.



    +-nlClin Chem 56(7):1071-9 (2010)
    42010Newborn screening for galactosemia: a review of 5 years of data and audit of a revised reporting approach.



    +-nlClin Chem 56(3):437-44 (2010)
    52005Newborn screening for lysosomal storage disorders.



    +-nlClin Chem 51(5):808-9 (2005) Millington DS
    62008Enhancing newborn screening for tyrosinemia type I.



    +-nlClin Chem 54(4):627-9 (2008) Pass KA
    72009National academy of clinical biochemistry laboratory medicine practice guidelines: follow-up testing for metabolic disease identified by expanded newborn screening using tandem mass spectrometry; executive summary.



    +-nlClin Chem 55(9):1615-26 (2009)
    82011Neonatal screening for metabolic and endocrine disorders.



    +-nlDtsch Arztebl Int 108(1-2):11-21; quiz 22 (2011)
    92004Clinical effectiveness and cost-effectiveness of neonatal screening for inborn errors of metabolism using tandem mass spectrometry: a systematic review.



    +-nlHealth Technol Assess 8(12):iii, 1-121 (2004)
    102008Newborn screening for all identifiable disorders with tandem mass spectrometry is cost effective: the negative case.



    +-nlAnn Acad Med Singapore 37(12 Suppl):36-3 (2008)
    112008Newborn screening for all identifiable disorders with tandem mass spectrometry is cost effective: supporting arguments.



    +-nlAnn Acad Med Singapore 37(12 Suppl):32-4 (2008)
    122008Neonatal screening--a global perspective.



    +-nlAnn Acad Med Singapore 37(12 Suppl):1-2 (2008)



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