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Showing articles 0 to 9 of 9 Filter Applied: enzyme,defect (Click to remove) Inherited Metabolic Diseases of the Nervous System, Inherited Hypeammonemia Adams & Victors Principles of Neurology, Chp 37, pg 952, Ropper, A.H.,et al, 2014 Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease Adams & Victors Principles of Neurology, Chp 37, pg 957, Ropper, A.H.,et al, 2014 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 Postpartum Coma and Death Due to Carbamoyl-Phosphate Synthetase I Deficiency Ann Int Med 120:216-217, Wong,L-J.C.,et al, 1994 Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus NEJM 322:1652-1669, Arn,P.H.,et al, 1990 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 Detection of Urea Cycle Enzymopathies in Childhood Arch Neurol 41:758-760, Trauner,D.A.,et al, 1984 Showing articles 0 to 9 of 9