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GENETIC ASPECTS OF CONGENITAL LONG QT SYNDROME [PDF]
Рациональная фармакотерапия в кардиологии, 2015 The main symptoms and clinical types of long QT syndrome are described. Molecular genetic diagnostics and updated approaches to the management of patients with long QT syndrome arepresented.
A. A. Chernova +2 more
doaj +2 more sources
Increased vulnerability of human ventricle to re-entrant excitation in hERG-linked variant 1 short QT syndrome [PDF]
, 2011 The short QT syndrome (SQTS) is a genetically heterogeneous condition characterized by abbreviated QT intervals and an increased susceptibility to arrhythmia and sudden death.
Hancox Jules C. +24 more
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Novel genes for QTc interval. How much heritability is explained, and how much is left to find? [PDF]
, 2010 The corrected QT (QTc) interval is a complex quantitative trait, believed to be influenced by several genetic and environmental factors. It is a strong prognostic indicator of cardiovascular mortality in patients with and without cardiac disease.
Spector, Timothy D. +9 more
core +1 more source
, 2023 University of Minnesota Duluth. Commission QT. (2023). Commission QT Bylaws.
University of Minnesota Duluth. Commission QT
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Žurnal Grodnenskogo Gosudarstvennogo Medicinskogo Universiteta, 2018 Long QT syndrome (LQTS) is a potentially life-threatening canalopathy, accompanied by prolonged QT interval on a 12-channel ECG, syncopal conditions and a high risk for sudden cardiac death due to the development of torsade de pointes (TdP ...
Kalatsei L. V., Snezhitskiy V. A.
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Sex differences in long QT syndrome
Frontiers in Cardiovascular Medicine, 2023 Long QT Syndrome (LQTS) is a rare, inherited channelopathy characterized by cardiac repolarization dysfunction, leading to a prolonged rate-corrected QT interval in patients who are at risk for malignant ventricular tachyarrhythmias, syncope, and even ...
Nuria Díez-Escuté +18 more
doaj +1 more source
Žurnal Grodnenskogo Gosudarstvennogo Medicinskogo Universiteta, 2018 Long QT syndrome (LQTS) is a potentially life-threatening channelopathy, accompanied by a prolonged QT interval on a 12-channel ECG, syncopal conditions and a high risk of sudden cardiac death due to the development of torsade de pointes (TdP ...
Kalatsei L. V., Snezhitskiy V. A.
doaj +1 more source
Long QT syndrome – Bench to bedside
Heart Rhythm O2, 2021 Long QT syndrome (LQTS) is a cardiovascular disorder characterized by an abnormality in cardiac repolarization leading to a prolonged QT interval and T-wave irregularities on the surface electrocardiogram. It is commonly associated with syncope, seizures,
Daniela Ponce-Balbuena, PhD +1 more
doaj +1 more source
Paediatric/young versus adult patients with long QT syndrome [PDF]
, 2021 Introduction Long QT syndrome (LQTS) is a less prevalent cardiac ion channelopathy than Brugada syndrome in Asia. The present study compared the outcomes between paediatric/young and adult LQTS patients. Methods This was a population-based retrospective
Gary Tse +9 more
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, 2019 Automated analysis of ECGs obtained from patients with long QT ...
Andrew Li (411246) +11 more
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