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Article

Hyperammonemia in women with a mutation at the ornithine carbamoyltransferase locus. A cause of postpartum coma.

The New England journal of medicine - 7 Jun 1990

Arn P H, Hauser E R, Thomas G H, Herman G, Hess D, Brusilow S W

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Share to Amino Acids
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 2342525
DOI: 10.1056/NEJM199006073222307

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hyperammonemia in women with a mutation at the ornithine carbamoyltransferase locus. A cause of postpartum coma.PMID 2342525Read ↗

Hyperammonemic coma in an ornithine transcarbamylase mutation carrier following antepartum corticosteroids.Semantic proximity Read ↗

Acute hyperammonaemic encephalopathy in a female newborn caused by a novel, de novo mutation in the ornithine transcarbamylase gene.Semantic proximity Read ↗

Y55D mutation in ornithine transcarbamylase associated with late-onset hyperammonemia in a male.Semantic proximity Read ↗

The clinical, biochemical, and molecular spectrum of ornithine transcarbamylase deficiency.Semantic proximity Read ↗

Clinical and biochemical heterogeneity in females of a large pedigree with ornithine transcarbamylase deficiency due to the R141Q mutation.Semantic proximity Read ↗

Ornithine Aminotransferase Deficiency in Differential Diagnosis of Neonatal Hyperammonemia: A Case with a Novel OAT Gene Mutation.Semantic proximity Read ↗

Hyperornithinaemia- hyperammonaemia- homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporterSemantic proximity Read ↗

Hyperammonemia, Lactic Acidosis, and Arrhythmia in a Newborn.Semantic proximity Read ↗

A critically ill postpartum woman with fatal hyperammonemic encephalopathy by intracranial venous sinus thrombosisSemantic proximity Read ↗

A Novel Two–Nucleotide Deletion in the Ornithine Transcarbamylase Gene Causing Fatal Hyperammonia in Early PregnancySemantic proximity Read ↗

Metabolic and neuropsychological phenotype in women heterozygous for ornithine transcarbamylase deficiency.Semantic proximity Read ↗

The phenotype of ostensibly healthy women who are carriers for ornithine transcarbamylase deficiency.Semantic proximity Read ↗

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