Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Liver dysfunction and steatosis in familial hypobetalipoproteinemia.

Clinical chemistry - 1 Jan 2005

Whitfield Amanda J, Barrett P Hugh R, Robertson Ken, Havlat Marek F, van Bockxmeer Frank M, Burnett John R

Abstract excerpt

A 32-year-old man presented with increases in serum alanine aminotransferase activity, iron concentration, and transferrin saturation, suggestive of hepatic dysfunction and iron overload. In addition, he had unusually low plasma concentrations of LDL-cholesterol and apolipoprotein (apo) B. Hepati...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to alpha 1-Antitrypsin
Share to Fatty Liver
Share to Hemochromatosis Protein

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Histocompatibility Antigens Class I

Share to Hypobetalipoproteinemias

Share to Liver Diseases

Share to Membrane Proteins

Source

Identifiers

PMID: 15514099
DOI: 10.1373/clinchem.2004.037978

Genes

HFE

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15514099-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Liver dysfunction and steatosis in familial hypobetalipoproteinemia.PMID 15514099Read ↗

Clinical and biochemical characteristics of individuals with low cholesterol syndromes: A comparison between familial hypobetalipoproteinemia and familial combined hypolipidemia.Semantic proximity Read ↗

Apolipoprotein B gene mutations and fatty liver in Japanese hypobetalipoproteinemia.Semantic proximity Read ↗

Fatty liver in heterozygous hypobetalipoproteinemia caused by a novel truncated form of apolipoprotein B.Semantic proximity Read ↗

Variable phenotypic expression of homozygous familial hypobetalipoproteinaemia due to novel APOB gene mutations.Semantic proximity Read ↗

Familial Hypobetalipoproteinemia: An Underrecognized Cause of Lean NASH.Semantic proximity Read ↗

Hemochromatosis, alcoholism and unhealthy dietary fat: a case report.Semantic proximity Read ↗

Abetalipoproteinemia and homozygous hypobetalipoproteinemia: a framework for diagnosis and management.Semantic proximity Read ↗

Hyperferritinemia is a risk factor for steatosis in chronic liver disease.Semantic proximity Read ↗

Hypobetalipoproteinemia and abetalipoproteinemia.Semantic proximity Read ↗

Combination of heterozygous APOB gene mutation with PNPLA3 and TM6SF2 variants promotes steatotic liver disease, cirrhosis and HCC developmentSemantic proximity Read ↗

Four novel mutations in APOB causing heterozygous and homozygous familial hypobetalipoproteinemia.Semantic proximity Read ↗

Familial hypobetalipoproteinemia: analysis of three Spanish cases with two new mutations in the APOB gene.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.