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Showing articles 0 to 9 of 9 Filter Applied: urea-cycle enzymopathies (Click to remove) A 27-Year Old Man with Rapidly Progressive Coma Neurol 85:e74-e78, Wong,J.M.,et al, 2015 A Young Man with Progressive Subcortical Lesions and Optic Nerve Atrophy Neurol 79:e63, Komatsuzaki, S.,et al, 2012 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 Inborn Errors of Urea Synthesis Ann Neurol 35:133-141, Batshaw,M.L., 1994 Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes J Pediatrics 122:423-425, Christodoulou,J.,et al, 1993 Ornithine Transcarbamylase Deficiency-A Cause of Bizarre Behavior in a Man NEJM 315:744-747, DiMagno,E.P.,et al, 1986 Neurologic Outcome in Children with Inborn Errors of Urea Synthesis NEJM 310:1500-1505, Msall,M.,et al, 1984 Treatment of Episodic Hyperammonemia in Children with Inborn Errors of Urea Synthesis NEJM 310:1630-1634, Brushlow,S.W.,et al, 1984 Clinical Features of Carbamyl Phosphate Synthetase-I Deficiency in an Adult Ann Neurol 16:90-93, Call,G.,et al, 1984 Showing articles 0 to 9 of 9