Results 41 to 50 of about 269,335 (318)
Fever-Induced QTc Prolongation and Ventricular Fibrillation in a Healthy Young Man [PDF]
, 2010 Long QT syndrome is associated with lethal tachyarrhythmia that can lead to syncope, seizure, and sudden death. Congenital long QT syndrome is a genetic disorder, characterized by delayed cardiac repolarization and prolongation of the QT interval on the ...
Amin +18 more
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GENETIC ASPECTS OF CONGENITAL LONG QT SYNDROME
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 +3 more sources
Meta-analysis of T peak –T end and T peak –T end /QT ratio for risk stratification in congenital long QT syndrome [PDF]
, 2018 Background and objectives: Congenital long QT syndrome (LQTS) predisposes affected individuals to ventricular tachycardia/fibrillation (VF/VF), potentially resulting in sudden cardiac death.
Baranchuk, Adrian M. +12 more
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The QT Intervals in Infancy and Time for Infantile ECG Screening for Long QT Syndrome [PDF]
, 2011 Background: Electrocardiographic and molecular studies have clarified an association between sudden infant death syndrome (SIDS) and long QT syndrome (LQTS), and few data are available for the QT interval in infancy from birth to 1 year of age ...
Yoshinaga, Masao +13 more
core +2 more sources
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.
doaj +1 more source
The Jervell and Lange-Nielsen syndrome; atrial pacing combined with ß-blocker therapy, a favorable approach in young high-risk patients with long QT syndrome? [PDF]
, 2016 BackgroundPatients with Jervell and Lange-Nielsen syndrome (JLNS) exhibit severe phenotypes that are characterized by congenital deafness, very long QT intervals, and high risk of life-threatening arrhythmias.
Døhlen, Gaute +4 more
core +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
Transient Long QT Development in a Patient with Takotsubo Cardiomyopathy
Journal of Cardiovascular Emergencies, 2016 QT interval prolongation on the electrocardiogram is considered a precursory sign for imminent, potentially lethal ventricular arrhythmias. Beside the inherited condition of long QT syndrome, numerous drugs, certain electrolyte disturbances and early ...
Czuriga Dániel +10 more
doaj +1 more source
A study of early afterdepolarizations in a model for human ventricular tissue [PDF]
, 2014 Sudden cardiac death is often caused by cardiac arrhythmias. Recently, special attention has been given to a certain arrhythmogenic condition, the long-QT syndrome, which occurs as a result of genetic mutations or drug toxicity. The underlying mechanisms
Kazbanov, Ivan +5 more
core +3 more sources
Resuscitation of sudden cardiac death caused by acute epileptic seizures: A case report
Journal of Acute Disease, 2016 Symptomatic long QT syndrome in pediatric patients is a life-threatening condition. Sometimes, this pathology can be misdiagnosed and erroneously managed as generalized epilepsy due to similar clinical manifestations.
Dana-Oliviana Geavlete +7 more
doaj +1 more source