Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysis.

doi:10.1194/jlr.P039875

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

Community

Back to search

Article

Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysis.

Journal of lipid research - 1 Dec 2013

Minicocci Ilenia, Santini Sara, Cantisani Vito, Stitziel Nathan, Kathiresan Sekar, Arroyo Juan Antonio, Martí Gertrudis, Pisciotta Livia, Noto Davide, Cefalù Angelo B, Maranghi Marianna, Labbadia Giancarlo, Pigna Giovanni, Pannozzo Fabio, Ceci Fabrizio, Ciociola Ester, Bertolini Stefano, Calandra Sebastiano, Tarugi Patrizia, Averna Maurizio, Arca Marcello

Abstract excerpt

Angiopoietin-like 3 (ANGPTL3) regulates lipoprotein metabolism by modulating extracellular lipases. Loss-of function mutations in ANGPTL3 gene cause familial combined hypolipidemia (FHBL2). The mode of inheritance and hepatic and vascular consequences of FHBL2 have not been fully elucidated. To get further insights on these aspects, we reevaluated the clinical and the biochemical characteristics of all reported...

Read the complete abstract on PubMed

Topics

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

Share to Angiopoietin-Like Protein 3

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Angiopoietin-like Proteins

Share to Angiopoietins

Share to Cardiovascular Diseases

Share to Fatty Liver

Share to Hypobetalipoproteinemias

Share to Lipids

Share to Lipoprotein(a)

Source

Open in PubMed Open full text

Identifiers

PMID: 24058201
DOI: 10.1194/jlr.P039875
PMCID: PMC3826694

Genes

ANGPTL3

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

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

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysis.PMID 24058201Read ↗

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

Mutations in the ANGPTL3 gene and familial combined hypolipidemia: a clinical and biochemical characterization.Semantic proximity Read ↗

Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia.Semantic proximity Read ↗

Effects of angiopoietin-like protein 3 deficiency on postprandial lipid and lipoprotein metabolism.Semantic proximity Read ↗

Familial combined hypolipidemia: angiopoietin-like protein-3 deficiencySemantic proximity Read ↗

ANGPTL3 Gene Variants in Subjects With Familial Combined HyperlipidemiaSemantic proximity Read ↗

Characterization of three kindreds with familial combined hypolipidemia caused by loss-of-function mutations of ANGPTL3.Semantic proximity Read ↗

ANGPTL3 gene variants in subjects with familial combined hyperlipidemia.Semantic proximity Read ↗

Familial combined hyperlipidemia: An overview of the underlying molecular mechanisms and therapeutic strategiesSemantic proximity Read ↗

Recent developments in the genetics of LDL deficiency.Semantic proximity Read ↗

Genetics of familial combined hyperlipidemia.Semantic proximity Read ↗

Hypotriglyceridemias/hypolipidemias.Semantic proximity Read ↗

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