Results 231 to 240 of about 38,746 (286)
Differential effects of non-selective and cardio-selective beta-blocker therapy on ECG parameters in long QT syndrome type 1. [PDF]
Int J Cardiol Heart VascRieder M +5 more
europepmc +1 more source
Congenital Long QT Syndrome: A Focus on Risk Stratification and Management. [PDF]
Rev Cardiovasc MedRanganathan D +3 more
europepmc +1 more source
Recurrent Ventricular Arrhythmia From Acquired Long QT Syndrome Due to Alcohol-Related Electrolyte Depletion. [PDF]
JACC Case RepZhang R +6 more
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Mechano-electrical feedback in transgenic rabbit models of long QT syndrome Type 2 and short QT syndrome Type 1. [PDF]
EuropaceAlerni N +15 more
europepmc +1 more source
Different beta-blockers for preventing arrhythmic events in patients with long QT syndrome: a network meta-analysis. [PDF]
Front Med (Lausanne)Jiang Y +6 more
europepmc +1 more source
Holter Monitor QT Dispersion and QTc-Dispersion in Pediatric Long QT Syndrome and Development of a Diagnostic and Arrhythmia Risk Prediction Model. [PDF]
J Am Heart AssocAllam H +8 more
europepmc +1 more source
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Praxis, 2010
#### Case scenario A 19 year old female student consulted her general practitioner about two recent episodes of syncope, both of which occurred while playing hockey. Her team mates reported that she collapsed suddenly with little warning, recovering rapidly within 30 seconds without confusion.
D J, Abrams, M A, Perkin, J R, Skinner
openaire +3 more sources
#### Case scenario A 19 year old female student consulted her general practitioner about two recent episodes of syncope, both of which occurred while playing hockey. Her team mates reported that she collapsed suddenly with little warning, recovering rapidly within 30 seconds without confusion.
D J, Abrams, M A, Perkin, J R, Skinner
openaire +3 more sources
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 +2 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 +2 more sources
American Journal of Critical Care, 2006
Some researchers claim that babies should be routinely tested for long QT syndrome (LQTS) by electrocardiogram (ECG) at around 3 weeks of age because it would be cost-effective and save lives. Bottom line. The ECG is neither sensitive nor specific to hereditary LQTS and can be hard to interpret in newborns.
Michele M, Pelter, Mary G, Carey
openaire +2 more sources
Some researchers claim that babies should be routinely tested for long QT syndrome (LQTS) by electrocardiogram (ECG) at around 3 weeks of age because it would be cost-effective and save lives. Bottom line. The ECG is neither sensitive nor specific to hereditary LQTS and can be hard to interpret in newborns.
Michele M, Pelter, Mary G, Carey
openaire +2 more sources