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Showing articles 0 to 7 of 7 Filter Applied: urea-cycle enzymopathies (Click to remove) 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 Progressive Subcortical Lesions and Optic Nerve Atrophy Neurol 79:e63, Komatsuzaki, S.,et al, 2012 Coma in a Young Anorexic Woman Lancet 357:1944, Blans,M.J.,et al, 2001 Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes J Pediatrics 122:423-425, Christodoulou,J.,et al, 1993 Arginase Deficiency Presenting as Cerebral Palsy Pediatrics 91:995-996, Scheuerle,A.E.,et al, 1993 Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus NEJM 322:1652-1669, Arn,P.H.,et al, 1990 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 7 of 7