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Showing articles 0 to 8 of 8 Filter Applied: ornithine transcarbamylase deficiency (Click to remove) 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 Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes J Pediatrics 122:423-425, Christodoulou,J.,et al, 1993 A Young Man with Recurrent Coma and Refractory Status Epilepticus JAMA Neurol 73:1243-1244, Sheikh, Z.,et al, 2016 Brain MR Imaging in Acute Hyperammonemic Encephalopathy Arising from Late-Onset Ornithine Transcarbamylase Deficiency AJNR 24:390-393, Takanashi,J-i.,et al, 2003 Coma in a Young Anorexic Woman Lancet 357:1944, Blans,M.J.,et al, 2001 Inborn Errors of Metabolism in Children Referred with Reye's Syndrome, A Changing Pattern JAMA 260:3167-3170, 3178-31801988., Rowe,P.C.,et al, 1988 Ornithine Transcarbamylase Deficiency-A Cause of Bizarre Behavior in a Man NEJM 315:744-747, DiMagno,E.P.,et al, 1986 Showing articles 0 to 8 of 8