Discover Community Create You

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

Pharmacological treatment of a Sardinian patient affected by Autosomal Recessive Hypercholesterolemia (ARH).

Journal of clinical lipidology - 1 Jan 2000

Muntoni Sandro, Pisciotta Livia, Muntoni Sergio, Bertolini Stefano

Abstract excerpt

BACKGROUND AND AIM: Previous studies have shown that patients with autosomal recessive hypercholesterolemia (ARH) resulting from mutations in LDLRAP1 gene have a less severe cardiovascular involvement than familial hypercholesterolemia homozygotes, lower levels of low-density lipoprotein choleste...

Read the complete abstract on PubMed

Topics

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

Share to Anticholesteremic Agents
Share to Apolipoprotein A-I
Share to Azetidines

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Ezetimibe

Share to Hyperlipoproteinemia Type III

Share to Proprotein Convertase 9

Share to Proprotein Convertases

Share to Rosuvastatin Calcium

Source

Identifiers

PMID: 25670367
DOI: 10.1016/j.jacl.2014.08.009

Genes

LDLRAP1
PCSK9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25670367-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Pharmacological treatment of a Sardinian patient affected by Autosomal Recessive Hypercholesterolemia (ARH).PMID 25670367Read ↗

From physiopathology to treatment of familial hypercholesterolemia: Existing and emerging pharmacotherapies.Semantic proximity Read ↗

A case of autosomal recessive hypercholesterolemia with a novel mutation in the LDLRAP1 geneSemantic proximity Read ↗

Management of autosomal recessive hypercholesterolemia in a patient with an LDLRAP1 mutation.Semantic proximity Read ↗

Current treatments for the management of homozygous familial hypercholesterolaemia: a systematic review and commentary.Semantic proximity Read ↗

The promising novel therapies for familial hypercholesterolemiaSemantic proximity Read ↗

New treatments on the horizon for familial hypercholesterolemia.Semantic proximity Read ↗

Optimal management of familial hypercholesterolemia: treatment and management strategiesSemantic proximity Read ↗

[LDL-apheresis in Sardinia, Italy].Semantic proximity Read ↗

Autosomal recessive hypercholesterolemia in a kindred of Syrian ancestry.Semantic proximity Read ↗

Homozygous autosomal dominant hypercholesterolaemiaSemantic proximity Read ↗

HEART UK statement on the management of homozygous familial hypercholesterolaemia in the United Kingdom.Semantic proximity Read ↗

Clinical and biochemical characterisation of patients with autosomal recessive hypercholesterolemia (ARH).Semantic proximity Read ↗

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