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2019 HRS/EHRA/APHRS/LAHRS expert consensus statement on catheter ablation of ventricular arrhythmias [PDF]
, 2019 Cuculich, Phillip, et al,
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Overlap of Congenital Deafness and Long QT Syndrome With Distinct Genetic Basis
Romana Pirah +5 more
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A case of congenital type 1 long QT syndrome which developed electrical storm with myocarditis
Satoshi Yamada +7 more
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JACC: Clinical Electrophysiology, 2022
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 understanding of LQTS has increased dramatically. The prevalence of LQTS is estimated to be ∼1:2,000, with a slight female predominance.
Andrew D, Krahn +6 more
openaire +4 more sources
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 understanding of LQTS has increased dramatically. The prevalence of LQTS is estimated to be ∼1:2,000, with a slight female predominance.
Andrew D, Krahn +6 more
openaire +4 more sources
Cardiac Electrophysiology Review, 1997
Many important advances have been made in the last several years regarding the molecular genetics and physiology of the congenital long QT syndrome. These findings have significantly changed our perceptions of the clinical manifestations of this disorder, and added new diagnostic and therapeutic strategies.
G Michael, Vincent +2 more
+6 more sources
Many important advances have been made in the last several years regarding the molecular genetics and physiology of the congenital long QT syndrome. These findings have significantly changed our perceptions of the clinical manifestations of this disorder, and added new diagnostic and therapeutic strategies.
G Michael, Vincent +2 more
+6 more sources
AACN Advanced Critical Care, 2010
The congenital long QT syndrome (LQTS) is considered to be one of the hereditary cardiac arrhythmia syndromes, nowadays also known as cardiac channelopathies. The syndrome is characterized by prolongation of the heart rate corrected QT-interval (QTc) on the 12-lead electrocardiogram (ECG).
Hubert F. Baars +1 more
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The congenital long QT syndrome (LQTS) is considered to be one of the hereditary cardiac arrhythmia syndromes, nowadays also known as cardiac channelopathies. The syndrome is characterized by prolongation of the heart rate corrected QT-interval (QTc) on the 12-lead electrocardiogram (ECG).
Hubert F. Baars +1 more
openaire +3 more sources
The congenital long QT syndrome
The Indian Journal of Pediatrics, 2002The long QT syndrome (LQTS) is a disorder of the electrical system of the heart, due to dysfunction of the ion channels and involving the repolarisation process. The inherited form occurs when there is a mutation in one of the genes which encode the making of a channel.
Preeti, Shanbag +4 more
openaire +2 more sources