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

Giant Ring Mitochondria in a Patient With Heart Failure and Cerebral White Matter Disease Resulting From an MT-TL1 Mitochondrial Gene Mutation.

Journal of cardiac failure - 1 Aug 2017

Houston Brian A, Judge Daniel P, Brown Emily, Halushka Marc, Barouch Lili A

Abstract excerpt

BACKGROUND: The presence of giant ring mitochondria on endomyocardial biopsy is rarely reported and does not have a well-defined differential diagnosis. METHODS: We report the case of a 54-year-old man with heart failure and preserved ejection fraction and left ventricular hypertrophy, initially thought to have an infiltrative cardiomyopathy. RESULTS: The patient was found to have extensive vacuolization caused...

Read the complete abstract on PubMed

Topics

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

Share to Genes, Mitochondrial
Share to Heart Failure

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Leukoencephalopathies

Share to Mutation

Share to Pedigree

Share to RNA, Transfer, Leu

Source

Identifiers

PMID: 28624653
DOI: 10.1016/j.cardfail.2017.06.001

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

Giant Ring Mitochondria in a Patient With Heart Failure and Cerebral White Matter Disease Resulting From an MT-TL1 Mitochondrial Gene Mutation.PMID 28624653Read ↗

Kickboxing a cardiomyopathy: mitochondrial sequencing provides answer for young athlete and her family.Semantic proximity Read ↗

A Multisystem Mitochondrial Disease Caused by a Novel MT-TL1 mtDNA Variant: A Case Report.Semantic proximity Read ↗

Progressive Myopathy and Respiratory Failure in a 7-Year-Old Boy With m.3251A>G MT-TL1 Mutation.Semantic proximity Read ↗

Giant Mitochondria in the Myocardium of a Patient With Mitochondrial CardiomyopathySemantic proximity Read ↗

Mitochondrial cardiomyopathies associated with the m.3243A>G mutation in the MT-TL1 gene: two sides of the same coin.Semantic proximity Read ↗

Detection of heteroplasmic mitochondrial DNA in single mitochondria.Semantic proximity Read ↗

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

Molecular biomarkers correlate with brain grey and white matter changes in patients with mitochondrial m.3243A > G mutation.Semantic proximity Read ↗

A novel, pathogenic dinucleotide deletion in the mitochondrial MT-TY gene causing myasthenia-like features.Semantic proximity Read ↗

Benign mitochondrial myopathy with exercise intolerance in a large multigeneration family due to a homoplasmic m.3250T>C mutation in MTTL1.Semantic proximity Read ↗

Mitochondrial myopathy with dystrophic features due to a novel mutation in the MTTM gene.Semantic proximity Read ↗

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