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Showing articles 0 to 7 of 7 Filter Applied: urea-cycle enzymopathies (Click to remove) A Young Man with Recurrent Coma and Refractory Status Epilepticus JAMA Neurol 73:1243-1244, Sheikh, Z.,et al, 2016 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 Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes J Pediatrics 122:423-425, Christodoulou,J.,et al, 1993 Clumsiness, Confusion, Coma, and Valproate Lancet 353:1408, Ellaway,C.J.,et al, 1999 Inborn Errors of Urea Synthesis Ann Neurol 35:133-141, Batshaw,M.L., 1994 Ornithine Transcarbamylase Deficiency-A Cause of Bizarre Behavior in a Man NEJM 315:744-747, DiMagno,E.P.,et al, 1986 Treatment of Episodic Hyperammonemia in Children with Inborn Errors of Urea Synthesis NEJM 310:1630-1634, Brushlow,S.W.,et al, 1984 Showing articles 0 to 7 of 7