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Charles Antzelevitch

Researcher at Lankenau Institute for Medical Research

Publications -  527
Citations -  58069

Charles Antzelevitch is an academic researcher from Lankenau Institute for Medical Research. The author has contributed to research in topics: Brugada syndrome & Repolarization. The author has an hindex of 118, co-authored 515 publications receiving 54661 citations. Previous affiliations of Charles Antzelevitch include University of Southern California & Main Line Health.

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Minimum Information about a Cardiac Electrophysiology Experiment (MICEE): Standardised reporting for model reproducibility, interoperability, and data sharing

T A Quinn, +62 more
TL;DR: A draft standard for recording, annotating, and reporting experimental data, called Minimum Information about a Cardiac Electrophysiology Experiment (MICEE) is presented, with the ultimate goal of developing a useful tool for cardiac electrophysiologists which facilitates and improves dissemination of the minimum information necessary for reproduction of cardiac electrophic research.
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In vivo human demonstration of phase 2 reentry.

Charles Antzelevitch
- 01 Aug 2005 - 
TL;DR: The presence of a prominent notch in the action potential of ventricular epicardium but not endocardium gives rise to a transmural voltage gradient during ventricular activation that manifests as a late delta wave following the QRS or what is commonly referred to as a J wave 1 or Osborn wave.
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Cellular basis for ST-segment changes observed during ischemia

TL;DR: 2 distinctly different mechanisms involving 1) loss of the epicardial action potential dome and 2) markedly delayed transmural conduction underlie the apparent ST-segment elevation encountered during acute ischemia are probed.
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The Brugada syndrome: clinical, genetic, cellular, and molecular abnormalities

TL;DR: The Brugada syndrome is an arrhythmic syndrome characterized by a right bundle branch block pattern and ST segment elevation in the right precordial leads of the electrocardiogram in conjunction with a high incidence of sudden death secondary to ventricular tachyarrhythmias.
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Novel mutations in domain I of SCN5A cause Brugada syndrome.

TL;DR: Three new SCN 5A mutations in Brugada syndrome patients are all located within domain I of SCN5A, a region not previously considered important in the development of ventricular arrhythmias.