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Article

Inherited long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease and other pregnancy complications

1 Apr 1999

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Identifiers

PMID: 10331463
DOI: 10.1016/s0146-0005(99)80044-5

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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

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

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Inherited long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease and other pregnancy complicationsPMID 10331463Read ↗

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The HELLP syndrome associated with fetal medium‐chain acyl‐CoA dehydrogenase deficiencySemantic proximity Read ↗

Recurrent acute fatty liver of pregnancy associated with a fatty-acid oxidation defect in the offspringSemantic proximity Read ↗

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Mitochondrial Dysfunction and Acute Fatty Liver of PregnancySemantic proximity Read ↗

A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women.Semantic proximity Read ↗

[Long-chain-3-hydroxyacyl-CoA dehydrogenase deficiency].Semantic proximity Read ↗

Acute fatty liver disease of pregnancySemantic proximity Read ↗

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