Results 91 to 100 of about 274,469 (144)
Long QT: Time to cut cholesterol?
International Journal of Cardiology: Heart & Vasculature, 2023 Jin Li, Flavien Charpentier, Ange Maguy
doaj +1 more source
Long QT syndrome: Genetic implications and drug influence [PDF]
, 2008 Gojković-Bukarica Ljiljana +1 more
core +1 more source
Prevalence of prolonged QTcinterval in electrocardiograms of 1 -12 year-old seizure patients
Nigerian Journal of PaediatricsBackground: Children with long QT intervals are prone to life-threatening ventricular arrhythmias which may lead to seizure and syncope and may be misdiagnosed as seizure.
Yousefi P +3 more
doaj
Approaching Fair Collision-Free Channel Access with Slotted ALOHA Using Collaborative Policy-Based Reinforcement Learning [PDF]
, 2020 de Alfaro, Luca +2 more
core
Some of the next articles are maybe not open access.
Related searches:
Related searches:
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
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
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