Results 221 to 230 of about 72,610 (277)

Beyond the Beat, Next-Generation Sequencing Discovery of Novel <i>RYR2</i> Gene Variant in Long QT Syndrome. [PDF]

Cardiol Res Pract
Kalayinia S, Jolfayi AG, Soheili A, Maleki M, Dalili M, Soveizi M, Komijani S.   +6 more
europepmc   +1 more source

A New High Penetrant Intronic Pathogenic Variant Related to Long QT Syndrome Type 2. [PDF]

J Clin Med
Rodríguez-Junquera M, Alén A, González-Urbistondo F, Rodríguez-Reguero JJ, Fernández B, Álvarez-Velasco R, Vazquez-Coto D, Vega-Prado LM, Avanzas P, Coto E, Gómez J, Lorca R.   +11 more
europepmc   +1 more source

Managing long QT syndrome patients, cooking, and common sense. [PDF]

Eur Heart J Suppl
Schwartz PJ, Dagradi F, Giovenzana FLF, Cerea P.   +3 more
europepmc   +1 more source

Exploring Exercise-induced Long QT: A Scoping Review of Reversibility Through Detraining and Distinction from Long QT Syndrome. [PDF]

US Cardiol
Wiradinata W, Subali AD, Aditya MR.
europepmc   +1 more source

Exploring the mechanisms of sex-specific proarrhythmia in long QT syndrome through computational modeling. [PDF]

Am J Physiol Heart Circ Physiol
Doherty I, Shetty R, Ni H, Morotti S, Grandi E.   +4 more
europepmc   +1 more source

Prioritizing repurposable drugs for Alzheimer's disease using network-based analysis with concurrent assessment of Long QT syndrome risk. [PDF]

Biotechnol Rep (Amst)
Funari A, De Smaele E, Paci P, Fiscon G.
europepmc   +1 more source

Temporal Variability of the Electromechanical Window in Long-QT Syndrome and Drug-Induced QT Prolongation: Value for Enhanced Arrhythmia-Risk Assessment

Deissler PM, Rahm A, Berkovitch A, Müller ME, Sikking M, Heymans S, Langenberg B, Moersdorf M, Rieder M, Nimani S, Odening KE, Dichtl W, Sabbag A, Volders PGA, ter Bekke RM.   +14 more
europepmc   +1 more source

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Long-QT-Syndrom

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

Long QT Syndrome

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

Congenital Long QT Syndrome

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, Zachary, Laksman, Raymond W, Sy, Pieter G, Postema, Michael J, Ackerman, Arthur A M, Wilde, Hui-Chen, Han   +6 more
openaire   +2 more sources