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Showing articles 0 to 8 of 8 Filter Applied: inborn errors of metabolism (Click to remove) A 27-Year Old Man with Rapidly Progressive Coma Neurol 85:e74-e78, Wong,J.M.,et al, 2015 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 Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Frequently Missed Diagnosis? Neurol 67:1519, Koppel,S.,et al, 2006 Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency Neurol 60:1413-1417, Pearl,P.L.,et al, 2003 Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation JNNP 69: 5-12, Gray,R.G.F. et al, 2000 Sjogren-Larsson Syndrome, Clinical and MRI/MRS Findings in FALDH-Deficient Patients Neurol 52:1345-1352,1307, Van Domburg,P.H.M.F.,et al, 1999 Clinicopath Conf Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992 Acute Extrapyramidal Syndrome in Methylmalonic Acidemia:"Metabolic Stroke"Involving the Globus Pallidus J Pediatr 113:1022-1027, Heidenreich,R.,et al, 1988 Showing articles 0 to 8 of 8