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Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients.
BACKGROUND Primary ventricular tachyarrhythmias are rarely seen in children. Among them, catecholaminergic polymorphic ventricular tachycardia has a poor spontaneous outcome. Its diagnosis is often… Expand
HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF,…
Developed in partnership with the Heart Rhythm Society (HRS), the European Heart Rhythm Association (EHRA), a registered branch of the European Society of Cardiology, and the Asia Pacific Heart… Expand
Executive Summary: HRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia Syndromes
Executive Summary: HRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia Syndromes Silvia G. Priori, MD, PhD, HRS Chairperson, Arthur… Expand
Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes.
- S. Priori, A. Wilde, +30 authors S. Quek
- Europace : European pacing, arrhythmias, and…
- 1 October 2013
This international consensus statement is the collaborative effort of three medical societies representing electrophysiology in North America, Europe, and Asian-Paciﬁc area: the Heart Rhythm Society… Expand
Catecholaminergic Polymorphic Ventricular Tachycardia
- A. Leenhardt, I. Denjoy, P. Guicheney
- Circulation. Arrhythmia and electrophysiology
- 1 October 2012
Sudden death because of cardiac arrhythmias in the young is a devastating event and remains underdiagnosed. The primary electric disorders responsible for polymorphic ventricular tachycardia (VT) or… Expand
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
Brugada syndrome is a rare cardiac arrhythmia disorder, causally related to SCN5A mutations in around 20% of cases. Through a genome-wide association study of 312 individuals with Brugada syndrome… Expand
Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human
- N. Roux-Buisson, Marine Cacheux, +19 authors I. Marty
- Biology, Medicine
- Human molecular genetics
- 14 March 2012
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited arrhythmogenic disease so far related to mutations in the cardiac ryanodine receptor (RYR2) or the cardiac calsequestrin… Expand
Mapping and Ablation of Ventricular Fibrillation Associated With Long-QT and Brugada Syndromes
Background—The long-QT and Brugada syndromes are important substrates of malignant ventricular arrhythmia. The feasibility of mapping and ablation of ventricular arrhythmias in these conditions has… Expand
Characteristics of recurrent ventricular fibrillation associated with inferolateral early repolarization role of drug therapy.
- M. Haïssaguerre, F. Sacher, +22 authors J. Clémenty
- Journal of the American College of Cardiology
- 17 February 2009
OBJECTIVES Our purpose was to evaluate the efficacy of antiarrhythmic drugs (AADs) in recurrent ventricular fibrillation (VF) associated with inferolateral early repolarization pattern on the… Expand
Short-coupled variant of torsade de pointes. A new electrocardiographic entity in the spectrum of idiopathic ventricular tachyarrhythmias.
- A. Leenhardt, E. Glaser, M. Burguera, M. Nürnberg, P. Maison-Blanche, P. Coumel
BACKGROUND Torsade de pointes is characterized not only by its particular ECG pattern but by its context of congenital or acquired long QT syndrome and the long coupling interval of the initial… Expand