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

Relationships among electrophysiological findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophy.

Circulation - 2 Mar 1999

Lazarus A, Varin J, Ounnoughene Z, Radvanyi H, Junien C, Coste J, Laforet P, Eymard B, Becane H M, Weber S, Duboc D

Abstract excerpt

BACKGROUND: Impulse-conduction abnormalities and arrhythmias are common in myotonic dystrophy (MD). This study was performed to determine whether a correlation exists between electrophysiological (EP) testing data and clinical status, heart function, or size of the DNA abnormality (cytosine-thymine-guanine sequence repeat). METHODS AND RESULTS: Eighty-three MD patients underwent invasive EP studies prompted...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Biochemical and Molecular Research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Electrocardiography

Share to Genetic Neurodegenerative Diseases

Share to Mutation

Share to Myotonic Dystrophy

Share to Trinucleotide Repeats

Source

Identifiers

PMID: 10051298
DOI: 10.1161/01.cir.99.8.1041

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Relationships among electrophysiological findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophy.PMID 10051298Read ↗

Cardiac Involvement in Emery-Dreifuss Muscular Dystrophy: From Arrhythmias to Heart Failure and Sudden Death: A Contemporary ReviewSemantic proximity Read ↗

Atrial arrhythmias in the young: early onset atrial arrhythmias preceding a diagnosis of a primary muscular dystrophy.Semantic proximity Read ↗

Association Between Mutation Size and Cardiac Involvement in Myotonic Dystrophy Type 1: An Analysis of the DM1-Heart Registry.Semantic proximity Read ↗

Relation of CTG expansion and clinical variables to electrocardiogram conduction abnormalities and sudden death in patients with myotonic dystrophy.Semantic proximity Read ↗

Clinical electrophysiologic tests and genotype correlations in muscle channelopathies.Semantic proximity Read ↗

Arrhythmias in the muscular dystrophies.Semantic proximity Read ↗

Cardiac features of Emery-Dreifuss muscular dystrophy caused by lamin A/C gene mutations.Semantic proximity Read ↗

Does cytosine-thymine-guanine (CTG) expansion size predict cardiac events and electrocardiographic progression in myotonic dystrophy?Semantic proximity Read ↗

High incidence of electrocardiogram abnormalities in young patients with duchenne muscular dystrophy.Semantic proximity Read ↗

Emery-Dreifuss muscular dystrophy Type 1 is associated with a high risk of malignant ventricular arrhythmias and end-stage heart failure.Semantic proximity Read ↗

Dilated, arrhythmogenic cardiomyopathy in emery-dreifuss muscular dystrophy due to the emerin splice-site mutation c.449 + 1G>A.Semantic proximity Read ↗

Optical Mapping Approaches on Muscleblind-Like Compound Knockout Mice for Understanding Mechanistic Insights Into Ventricular Arrhythmias in Myotonic Dystrophy.Semantic proximity Read ↗

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