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Showing articles 0 to 13 of 13 Filter Applied: inborn errors of metabolism (Click to remove) An Infant with Developmental Delay, Epileptic Spasms, and Acrocyanosis Neurol 94:939-942, Madaan, P.,et al, 2020 A 27-Year Old Man with Rapidly Progressive Coma Neurol 85:e74-e78, Wong,J.M.,et al, 2015 Inherited Metabolic Diseases of the Nervous System, The Phenylketonuria Adams & Victors Principles of Neurology, Chp 37, pg 968, Ropper, A.H.,et al, 2014 Cognitive Delay in a 7-year-old Girl Neurol 81: e148-e150, Cachia, D. & Stine, C., 2013 Overview of Phenylketonuria UptoDate (May), Bodamer,O.A., 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 Aromatic L-Amino Acid Decarboxylase Deficiency Neurol 62:1058-1065, Pons,R.,et al, 2004 Practice Parameter: Evaluation of the Child with Global Developmental Delay Neurol 60:367-380, Shevell,M.,et al, 2003 Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients Ann Neurol 44:720-730,713, Baumgartner,M.R.,et al, 1998 Postpartum Coma and Death Due to Carbamoyl-Phosphate Synthetase I Deficiency Ann Int Med 120:216-217, Wong,L-J.C.,et al, 1994 Neurologic Crises in Hereditary Tyrosinemia NEJM 322:432-437, Mitchell,G.,et al, 1990 GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families Hum Genet 70:347-354, Giugliani,R.,et al, 1985 Showing articles 0 to 13 of 13