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A Young Man with Progressive Subcortical Lesions and Optic Nerve Atrophy
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Mysteriod Episodic Coma
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Coma in a Young Anorexic Woman
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Clumsiness, Confusion, Coma, and Valproate
Lancet 353:1408, Ellaway,C.J.,et al, 1999
Inborn Errors of Urea Synthesis
Ann Neurol 35:133-141, Batshaw,M.L., 1994
Postpartum Coma and Death Due to Carbamoyl-Phosphate Synthetase I Deficiency
Ann Int Med 120:216-217, Wong,L-J.C.,et al, 1994
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
Inborn Errors of Metabolism in Children Referred with Reye's Syndrome, A Changing Pattern
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Ornithine Transcarbamylase Deficiency-A Cause of Bizarre Behavior in a Man
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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
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Detection of Urea Cycle Enzymopathies in Childhood
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Clinical Features of Carbamyl Phosphate Synthetase-I Deficiency in an Adult
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