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Showing articles 0 to 7 of 7 Filter Applied: urea-cycle enzymopathies (Click to remove) Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes J Pediatrics 122:423-425, Christodoulou,J.,et al, 1993 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 A Young Man with Recurrent Coma and Refractory Status Epilepticus JAMA Neurol 73:1243-1244, Sheikh, Z.,et al, 2016 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, Inherited Hypeammonemia Adams & Victors Principles of Neurology, Chp 37, pg 952, Ropper, A.H.,et al, 2014 Arginase Deficiency Presenting as Cerebral Palsy Pediatrics 91:995-996, Scheuerle,A.E.,et al, 1993 Neurologic Outcome in Children with Inborn Errors of Urea Synthesis NEJM 310:1500-1505, Msall,M.,et al, 1984 Showing articles 0 to 7 of 7