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Showing articles 0 to 6 of 6 Filter Applied: inborn errors of metabolism,screening (Click to remove) Newborn Screening and Presymptomatic Treatment of Metachromatic Leukodystrophy NEJM 391:1256-1258, Laugwitz,L.,et al, 2024 "Im fine; Im just waiting for my disease" The New and Growing Class of Presymptomatic Patients Neurol 77:522-523, Kwon, J.M.et al, 2011 Overview of Phenylketonuria UptoDate (May), Bodamer,O.A., 2008 Response of Anti-NMDA Receptor Encephalitis Without Tumor to Immunotherapy Including Rituximab Neurol 71:1921-1923, Ishiura,H.,et al, 2008 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 Phenylketonuria eMedicine (December), Arnold,G.L., 2007 Showing articles 0 to 6 of 6