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Showing articles 0 to 7 of 7 Filter Applied: ornithine transcarbamylase deficiency (Click to remove) 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 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 Clumsiness, Confusion, Coma, and Valproate Lancet 353:1408, Ellaway,C.J.,et al, 1999 Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus NEJM 322:1652-1669, Arn,P.H.,et al, 1990 Showing articles 0 to 7 of 7