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

[Mixed dyslipoproteinemias: new therapeutic opportunities].

Annali italiani di medicina interna : organo ufficiale della Societa italiana di medicina interna - 1 Oct 1995

Capurso A

Abstract excerpt

Familial combined hyperlipoproteinemia (FCHL) is a dyslipidemic syndrome prevalent in patients with coronary artery disease and characterized by variable expression of hypercholesterolemia, hypertriglyceridemia in a given family, with either or both present in affected individuals. Efforts to ref...

Topics

Humans
Hyperlipoproteinemias
Hypolipidemic Agents
Phenotype

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 8562265

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-8562265-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Mixed dyslipoproteinemias: new therapeutic opportunities].PMID 8562265Read ↗

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

[Familial combined hyperlipidemia].Semantic proximity Read ↗

Dysbetalipoproteinaemia: a mixed hyperlipidaemia of remnant lipoproteins due to mutations in apolipoprotein E.Semantic proximity Read ↗

Combined hyperlipidemia: familial but not (usually) monogenic.Semantic proximity Read ↗

Familial combined hyperlipidemia and hyperlipoprotein(a) as phenotypic mimics of familial hypercholesterolemia: Frequencies, associations and predictions.Semantic proximity Read ↗

Familial combined hyperlipidemia in children: clinical expression, metabolic defects, and management.Semantic proximity Read ↗

Small, dense LDL and elevated apolipoprotein B are the common characteristics for the three major lipid phenotypes of familial combined hyperlipidemia.Semantic proximity Read ↗

Genetic dissection of familial combined hyperlipidemia.Semantic proximity Read ↗

[Hypercholesterolemia ].Semantic proximity Read ↗

Subclasses of low-density lipoprotein and very low-density lipoprotein in familial combined hyperlipidemia: relationship to multiple lipoprotein phenotype.Semantic proximity Read ↗

[Familial lipoprotein lipase deficiency].Semantic proximity Read ↗

[Familial lipoprotein lipase deficiency].Semantic proximity Read ↗

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