Hyperammonemic coma due to parenteral nutrition in a woman with heterozygous ornithine transcarbamylase deficiency

The Metabolic Basis of Inherited Disease.

Annals of Internal Medicine · 1988 · 7.8K citations

Life Sciences, Genetics, Molecular Genetics +13

The Metabolic Basis of Inherited Disease

Annals of Internal Medicine · 1990 · 4K citations

Life Sciences, Genetics, Molecular Genetics +13

Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus

Pamela Arn, Elizabeth R. Hauser, George H. Thomas et al. · New England Journal of Medicine · 1990 · 182 citations · Full text

Life Sciences, Genetics, Pediatrics +12

Natural History of Symptomatic Partial Ornithine Transcarbamylase Deficiency

Peter C. Rowe, Stephen L. Newman, Saul W. Brusilow · New England Journal of Medicine · 1986 · 137 citations

Life Sciences, Neurology, Pediatrics +17

Risk of serious illness in heterozygotes for ornithine transcarbamylase deficency

Mark L. Batshaw, Michael E. Msall, Arthur L. Beaudet et al. · The Journal of Pediatrics · 1986 · 131 citations

Life Sciences, Genetics, Molecular Genetics +12