Results 191 to 200 of about 169,795 (221)

Oral Abstracts for the 17th Asia Pacific Heart Rhythm Society (APHRS) Scientific Sessions

Journal of Arrhythmia, Volume 41, Issue 2, April 2025.
wiley   +1 more source

Standard Poster Abstracts for the 17th Asia Pacific Heart Rhythm Society (APHRS) Scientific Sessions

Journal of Arrhythmia, Volume 41, Issue 2, April 2025.
wiley   +1 more source

Spontaneous Onset of Torsade de Pointes in Long-QT Syndrome and the Role of Sympathovagal Imbalance.

, 2001
Akira Fujiki, Kunihiro Nishida, Koichi Mizumaki, Hidehiko Nagasawa, Mayumi Shimono, Hiroshi Inoue   +5 more
openalex   +2 more sources

The Canine Purkinje Fiber: An In Vitro Model System for Acquired Long QT Syndrome and Drug-Induced Arrhythmogenesis

, 2001
Gary Gintant, James T. Limberis, Jeff S. McDermott, Craig D. Wegner, Bryan F. Cox   +4 more
openalex   +1 more source

Mortality and causes of death in LQT1 and LQT2 type of long QT syndrome based on systematic survey in finnish pedigrees Heikki Swan, Kirsi Piippo, P�ivi Laitinen, Kimmo Kontula, Matti Viitasalo, Lauri Toivonen. Helsinki University Department of Medicine, Helsinki, Finland

, 2001

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DHPLC analysis of potassium ion channel genes in congenital long QT syndrome

, 2002
Roselie Jongbloed, Carlo Marcelis, Crool Velter, Pieter A. Doevendans, Joep Geraedts, Hubert J.M. Smeets   +5 more
openalex   +1 more source

LONG QT SYNDROME [PDF]

Cardiology Clinics, 2000
In conclusion, much has been learned in the past several years regarding the molecular biology of LQTS, and this information has been directly applicable to the clinical care of patients with this syndrome. The knowledge also has been of considerable importance for understanding the molecular basis of arrhythmias in general and is providing insights ...
Michael C. Sanguinetti
openaire   +4 more sources

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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.
Mary G. Carey, Michele M. Pelter
openaire   +5 more sources

The long QT syndrome

Current Problems in Cardiology, 1980
The still inadequate but increasing awareness of the existence of the idiopathic long QT syndrome (LQTS) has provided ample evidence that, as suggested by many, this disease is far from being rare. This notion, coupled with the unusual pathophysiological characteristics and with the high degree of lethality in untreated patients, explains why the LQTS ...
openaire   +4 more sources

Long QT Syndrome and Short QT Syndrome

Progress in Cardiovascular Diseases, 2008
The long QT syndrome (LQTS) is a genetic disorder characterized by prolongation of the QT interval in the electrocardiogram (ECG) and a propensity to torsades de pointes ventricular tachycardia frequently leading to syncope, cardiac arrest, or sudden death usually in young otherwise healthy individuals.
Iwona Cygankiewicz, Wojciech Zareba
openaire   +3 more sources