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

Laminopathies: from the heart of the cell to the clinics.

Current opinion in neurology - 1 Oct 2004

Benedetti Sara, Merlini Luciano

Abstract excerpt

PURPOSE OF REVIEW: This review outlines recent advances in the clinical, genetic and molecular aspects of laminopathies, an expanding group of disorders caused by mutations of the lamin A/C gene. RECENT FINDINGS: Mutations in lamin A/C were originally described in skeletal and cardiac muscle disorders. It has subsequently been shown that partial lipodystrophy syndromes with or without developmental abnormalities...

Read the complete abstract on PubMed

Topics

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

Share to Cardiomyopathies
Share to Lamins
Share to Lipodystrophy

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Muscular Diseases

Share to Mutation

Share to Neuromuscular Diseases

Source

Identifiers

PMID: 15367859
DOI: 10.1097/00019052-200410000-00005

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Laminopathies: from the heart of the cell to the clinics.PMID 15367859Read ↗

Lamin A/C and cardiac diseases.Semantic proximity Read ↗

[Laminopathies: one gene, several diseases].Semantic proximity Read ↗

"Laminopathies": a wide spectrum of human diseases.Semantic proximity Read ↗

Laminopathies: multiple disorders arising from defects in nuclear architecture.Semantic proximity Read ↗

Heart involvement in lamin A/C related diseases.Semantic proximity Read ↗

[Diseases associated with lamin A/C gene defects: what the clinical cardiologist ought to know].Semantic proximity Read ↗

Lamin A/C deficiency as a cause of familial dilated cardiomyopathySemantic proximity Read ↗

The structure and function of lamin A/C: Special focus on cardiomyopathy and therapeutic interventions.Semantic proximity Read ↗

[Laminopathies: lipodystrophies, insulin resistance, syndromes of accelerated ageing... and others].Semantic proximity Read ↗

Lamin A/C mutations in dilated cardiomyopathy.Semantic proximity Read ↗

Genetic and Pathophysiological Basis of Cardiac and Skeletal Muscle Laminopathies.Semantic proximity Read ↗

Laminopathies; Mutations on single gene and various human genetic diseases.Semantic proximity Read ↗

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