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Showing articles 0 to 4 of 4 Filter Applied: inborn errors of metabolism,screening (Click to remove) Overview of Phenylketonuria UptoDate (May), Bodamer,O.A., 2008 Phenylketonuria eMedicine (December), Arnold,G.L., 2007 Newborn Screening and Presymptomatic Treatment of Metachromatic Leukodystrophy NEJM 391:1256-1258, Laugwitz,L.,et al, 2024 Outcome of Neonatal Screening for Medium-Chain acyl-CoA Dehydrogenase Deficiency in Australia: A Cohort Study Lancet 369:37-42,5, Wilcken,B.,et al, 2007 Showing articles 0 to 4 of 4