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Showing articles 0 to 12 of 12 Filter Applied: genetic neurologic disorders (Click to remove) A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency Neurol 100:206-212, Stamm,B.,et al, 2023 A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction Ann Neurol 79:507-519, Vodopivec, I.,et al, 2016 Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use Neurol 84:e165-e169, Whitlock, J.B.,et al, 2015 Coma in a Young Anorexic Woman Lancet 357:1944, Blans,M.J.,et al, 2001 Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes J Pediatrics 122:423-425, Christodoulou,J.,et al, 1993 New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications BMJ 304:1647-1648, Mitchell,S.&Bradbeer,C., 1992 Brief Report:Autosomal Dominant Familial Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia NEJM 327:1069-1074, Bilous,R.W.,et al, 1992 Clinical & Laboratory Findings in the Oculocerebrorenal Syndrome of Lowe, with Special Ref to Growth & Renal Function NEJM 324:1318-1325, Charnas,L.R.,et al, 1991 Anderson-Fabry Disease Editorial, Lancet 336:24-251990., , 1990 Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus NEJM 322:1652-1669, Arn,P.H.,et al, 1990 Ornithine Transcarbamylase Deficiency-A Cause of Bizarre Behavior in a Man NEJM 315:744-747, DiMagno,E.P.,et al, 1986 Phosphorylase Deficiency In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986 Showing articles 0 to 12 of 12