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

Mitochondrial DNA related cardiomyopathies.

Frontiers in bioscience (Elite edition) - 1 Jan 2012

Mohammed Shamayel, Bahitham Wesam, Chan Alicia, Chiu Brian, Bamforth Fiona, Sergi Consolato

Abstract excerpt

Cardiomyopathies are a heterogeneous group of diseases characterized by impaired heart muscle function. Over the last few years, interest in mitochondrial cardiomyopathies has been galvanized by a number of significant molecular biology discoveries. There is overwhelming evidence that genetic factors play a pivotal role in the pathogenesis of primary cardiomyopathies. Mitochondrial cardiomyopathy is a...

Read the complete abstract on PubMed

Topics

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

Share to Cardiomyopathies
Share to DNA, Mitochondrial
Share to Mutation

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

Share to Oxidative Phosphorylation

Source

Identifiers

PMID: 22201986
DOI: 10.2741/491

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

Mitochondrial DNA related cardiomyopathies.PMID 22201986Read ↗

Molecular Epidemiology of Mitochondrial Cardiomyopathy: A Search Among Mitochondrial and Nuclear Genes.Semantic proximity Read ↗

Cardiac Involvement in Mitochondrial Disorders.Semantic proximity Read ↗

Mitochondrial diseases and the heart: an overview of molecular basis, diagnosis, treatment and clinical course.Semantic proximity Read ↗

Cardiac involvement in mitochondrial DNA disease: clinical spectrum, diagnosis, and management.Semantic proximity Read ↗

Mitochondrial Genome Variants as a Cause of Mitochondrial Cardiomyopathy.Semantic proximity Read ↗

Mitochondrial cardiomyopathy: pathophysiology, diagnosis, and management.Semantic proximity Read ↗

Mitochondrial disease and the heartSemantic proximity Read ↗

Mitochondrial Mutations in Cardiac Disorders.Semantic proximity Read ↗

Mitochondrial cardiomyopathy: molecular and biochemical analysis.Semantic proximity Read ↗

[Advances in the molecular genetics of nuclear gene mutations causing pediatric mitochondrial cardiomyopathy].Semantic proximity Read ↗

Inherited CardiomyopathiesSemantic proximity Read ↗

Mitochondrial DNA, mitochondrial dysfunction, and cardiac manifestations.Semantic proximity Read ↗

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