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

Electron Microscopic Findings Are an Important Aid for Diagnosing Mitochondrial Cardiomyopathy With Mitochondrial DNA Mutation 3243A>G.

Circulation. Heart failure - 1 Jul 2016

Takemura Genzou, Onoue Kenji, Kashimura Takeshi, Kanamori Hiromitsu, Okada Hideshi, Tsujimoto Akiko, Miyazaki Nagisa, Nakano Tomoya, Sakaguchi Yasuhiro, Saito Yoshihiko

Abstract excerpt

No abstract is available from the source.

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 Heart Failure

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Microscopy, Electron

Share to Mitochondria

Share to Mutation

Share to Myocardium

Source

Identifiers

PMID: 27402860
DOI: 10.1161/CIRCHEARTFAILURE.116.003283

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Electron Microscopic Findings Are an Important Aid for Diagnosing Mitochondrial Cardiomyopathy With Mitochondrial DNA Mutation 3243A>G.PMID 27402860Read ↗

Comparison of electron microscopic findings and clinical presentation in three patients with mitochondrial cardiomyopathy caused by the mitochondrial DNA mutation m.3243A > G.Semantic proximity Read ↗

Common methods in mitochondrial research (Review).Semantic proximity Read ↗

Presentation and Diagnostic Evaluation of Mitochondrial Disease.Semantic proximity Read ↗

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

Mitochondrial cardiomyopathy due to m.3243A>G mitochondrial DNA mutation presenting in late adulthood: a case report.Semantic proximity Read ↗

Presentation and diagnosis of mitochondrial disorders in children.Semantic proximity Read ↗

Cardiomyopathy is common in patients with the mitochondrial DNA m.3243A>G mutation and correlates with mutation load.Semantic proximity Read ↗

Hypertrophic Cardiomyopathy Attributable to Mitochondrial DNA Mutation Diagnosed by Pathology and Gene Sequencing.Semantic proximity Read ↗

Biochemical methods for diagnosis of mitochondrial cytopathies: introduction and perspectives.Semantic proximity Read ↗

Ultrastructural mitochondrial modifications characteristic of mitofusin 2 mutations (CMT2A).Semantic proximity Read ↗

Sudden adult death syndrome in m.3243A>G-related mitochondrial disease: an unrecognized clinical entity in young, asymptomatic adults.Semantic proximity Read ↗

Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy.Semantic proximity Read ↗

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