Prolonged repolarization in long QT3 syndrome: unusual electrocardiographic findings
T Raviña, JA Lapuerta… - International …, 2002 - internationaljournalofcardiology.com
Congenital long QT syndrome is a cardiovascular with a LQT3 ECG pattern and unusual
electrocardisease characterised by prolonged ventricular repo- diographic findings …
electrocardisease characterised by prolonged ventricular repo- diographic findings …
Congenital long QT syndrome
GM Vincent, K Timothy, L Zhang - Cardiac Electrophysiology Review, 2002 - Springer
The congenital Long QT syndrome (LQTS) is a primary electrophysiologic disorder of the
heart caused by mutations of genes which encode three different cardiac ion channels. The …
heart caused by mutations of genes which encode three different cardiac ion channels. The …
Congenital long QT syndrome: a case report of LQT2 and LQT13 in a neonate
R Bond, A Blaufox, B Goldner, A Patel - Europace, 2014 - academic.oup.com
Long QT syndrome (LQTS) is a disorder of ventricular myocardial repolarization
characterized by a prolonged QT interval on the electrocardiogram (ECG). At least 12 …
characterized by a prolonged QT interval on the electrocardiogram (ECG). At least 12 …
Congenital long QT syndrome
JM Lupoglazoff, I Denjoy, P Guicheney… - Archives de Pediatrie …, 2001 - europepmc.org
Long QT syndrome (LQTS) is a clinically and genetically heterogenous syndrome
characterized by a lengthening of the QT interval on the surface ECG and a propensity to …
characterized by a lengthening of the QT interval on the surface ECG and a propensity to …
Long QT syndrome
GM Vincent - Cardiology clinics, 2000 - Elsevier
The long QT syndrome (LQTS) is a disorder of cardiac ion channels that affect
repolarization. The characteristic manifestations are prolongation of the QT interval and T …
repolarization. The characteristic manifestations are prolongation of the QT interval and T …
The long QT syndrome: molecular and genetic aspects
C Napolitano, SG Priori - Cardiac Repolarization: Bridging Basic and …, 2003 - Springer
Abstract The Long QT syndrome (LQTS) is an inherited arrhythmogenic disease occurring in
the structurally normal heart that may cause sudden death and that usually manifests in …
the structurally normal heart that may cause sudden death and that usually manifests in …
Inherited long QT syndromes: be mindful of the potassium level
JR Kapoor - Journal of the American College of Cardiology, 2008 - jacc.org
Management of inherited channelopathies has benefited a great deal from advances in our
understanding of the pathophysiological basis of associated arrhythmogenesis. The …
understanding of the pathophysiological basis of associated arrhythmogenesis. The …
Prevalence of early repolarization in congenital long QT syndrome. A combination of early and delayed repolarization
M Audoubert, A Rollin, A Duparc… - European Heart …, 2013 - academic.oup.com
Introduction: Early Repolarization (ER) in Brugada or short QT syndrome is common and
has been associated to a less favourable outcome. Even if apparently paradoxical, ER can …
has been associated to a less favourable outcome. Even if apparently paradoxical, ER can …
Syndrome du QT long congénital
JM Lupoglazoff, I Denjoy, P Guicheney… - Archives de pédiatrie, 2001 - Elsevier
Long QT syndrome (LQTS) is a clinically and genetically heterogenous syndrome
characterized by a lengthening of the QT interval on the surface ECG and a propensity to …
characterized by a lengthening of the QT interval on the surface ECG and a propensity to …
[HTML][HTML] Congenital Long QT Syndrome (LQTS) in Infancy: A Challenging Case
M Aldirawi, R Musa, M Hamdi, L Yavuz - Cureus, 2024 - ncbi.nlm.nih.gov
Long QT syndrome (LQTS), is an arrhythmia disorder, related to ventricular myocardial
repolarization characterized by a prolonged QT interval on the electrocardiogram that can …
repolarization characterized by a prolonged QT interval on the electrocardiogram that can …