International recommendations for electrocardiographic interpretation in athletes

S Sharma, JA Drezner, A Baggish, M Papadakis… - Journal of the American …, 2017 - jacc.org
Sudden cardiac death (SCD) is the leading cause of mortality in athletes during sport. A
variety of mostly hereditary, structural, or electrical cardiac disorders are associated with …

Congenital long QT syndrome

AD Krahn, Z Laksman, RW Sy, PG Postema… - Clinical …, 2022 - jacc.org
Congenital long QT syndrome (LQTS) encompasses a group of heritable conditions that are
associated with cardiac repolarization dysfunction. Since its initial description in 1957, our …

International criteria for electrocardiographic interpretation in athletes: consensus statement

JA Drezner, S Sharma, A Baggish… - British journal of sports …, 2017 - bjsm.bmj.com
Sudden cardiac death (SCD) is the leading cause of mortality in athletes during sport. A
variety of mostly hereditary, structural or electrical cardiac disorders are associated with …

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership …

MJ Ackerman, SG Priori, S Willems, C Berul… - Europace, 2011 - academic.oup.com
1From Mayo Clinic, Rochester, Minnesota; 2Fondazione Salvatore Maugeri University of
Pavia, Pavia, Italy and New York University, New York, New York; 3University Hospital …

The endophenotype concept in psychiatry: etymology and strategic intentions

II Gottesman, TD Gould - American journal of psychiatry, 2003 - Am Psychiatric Assoc
Endophenotypes, measurable components unseen by the unaided eye along the pathway
between disease and distal genotype, have emerged as an important concept in the study of …

Prevalence of the congenital long-QT syndrome

PJ Schwartz, M Stramba-Badiale, L Crotti… - Circulation, 2009 - Am Heart Assoc
Background—The prevalence of genetic arrhythmogenic diseases is unknown. For the long-
QT syndrome (LQTS), figures ranging from 1: 20 000 to 1: 5000 were published, but none …

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

ME Curran, I Splawski, KW Timothy, GM Vincen… - Cell, 1995 - Elsevier
To identify genes involved in cardiac arrhythmia, we investigated patients with long OT
syndrome (LOT), an inherited disorder causing sudden death from a ventricular …

Sudden death in young competitive athletes: clinical, demographic, and pathological profiles

BJ Maron, J Shirani, LC Poliac, R Mathenge… - Jama, 1996 - jamanetwork.com
Objective.—To develop clinical, demographic, and pathological profiles of young
competitive athletes who died suddenly. Design.—Systematic evaluation of clinical …

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

Q Wang, J Shen, I Splawski, D Atkinson, Z Li… - Cell, 1995 - cell.com
Long QT syndrome (LQT) is an inherited disorder that causes sudden death from cardiac
arrhythmias, specifically torsade de pointes and ventricular fibrillation. We previously …

Catecholaminergic polymorphic ventricular tachycardia in children: a 7-year follow-up of 21 patients

A Leenhardt, V Lucet, I Denjoy, F Grau, DD Ngoc… - Circulation, 1995 - Am Heart Assoc
Background Primary ventricular tachyarrhythmias are rarely seen in children. Among them,
catecholaminergic polymorphic ventricular tachycardia has a poor spontaneous outcome. Its …