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Fetal Presentation of Congenital Long QT Syndrome
Pediatric Cardiology, 1999Thirty-two-week prenatal ultrasound revealed a fetal heart rate of 100 bpm with decreased variability on the heart rate tracing. Echocardiogram documented normal anatomy and sinus bradycardia. Newborn electrocardiogram revealed sinus rhythm at 100 bpm with a QTc of 0.657.
M T, Donofrio +3 more
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Anesthesia for Patients with Congenital Long QT Syndrome
Anesthesiology, 2005Long QT syndrome is a malfunction of cardiac ion channels resulting in impaired ventricular repolarization that can lead to a characteristic polymorphic ventricular tachycardia known as torsades de pointes. Stressors, by increasing sympathetic tone, and drugs can provoke torsade de pointes, leading to syncope, seizures, or sudden cardiac death in these
Susan J, Kies +4 more
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Anesthesia eJournal
Context: Congenital long QT syndrome (cLQTS) is the most common genetic cardiac ion channelopathy in the US. Patients with cLQTS are at risk for ventricular tachycardia (VT) in the “torsades de pointes” (TdP) pattern from physical and emotional stress, including during the perioperative period.
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Context: Congenital long QT syndrome (cLQTS) is the most common genetic cardiac ion channelopathy in the US. Patients with cLQTS are at risk for ventricular tachycardia (VT) in the “torsades de pointes” (TdP) pattern from physical and emotional stress, including during the perioperative period.
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Genetics of Congenital Long Qt Syndrome and Brugada Syndrome
Future Cardiology, 2008The inherited cardiac arrhythmias including congenital and acquired long QT syndrome (LQTS), Brugada syndrome, progressive cardiac conduction defect, catecholaminergic polymorphic ventricular tachycardia, arrhythmogenic right ventricular cardiomyopathy, familial atrial fibrillation, familial sick sinus syndrome and short QT syndrome, are linked to ...
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[Congenital long QT syndrome].
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 2001Long QT syndrome (LQTS) is a clinically and genetically heterogenous syndrome characterized by a lengthening of the QT interval on the surface ECG and a propensity to severe ventricular arrhythmias such as torsades de pointes and ventricular fibrillation, leading eventually to syncope and sudden death.
J M, Lupoglazoff +4 more
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[Congenital long QT syndrome].
Presse medicale (Paris, France : 1983), 1998SEVERAL FORMS: Congenital long QT syndrome is a clinically (with and without deafness) and genetically (recessive or dominant autosomal inheritance) heterogeneous entity characterized by a long QT interval on the ECG associated with the risk of severe ventricular arrhythmia (torsade de pointes, ventricular fibrillation) and subsequent syncope or sudden
Lupoglazoff, J +5 more
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Precision therapy in congenital long QT syndrome
Trends in Cardiovascular MedicineLong QT syndrome (LQTS) is a potentially life-threatening, but highly treatable genetic heart disease. LQTS-directed therapies often consist of beta-blockers (BBs), left cardiac sympathetic denervation (LCSD), and/or an implantable cardioverter defibrillator (ICD).
Raquel, Neves +5 more
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Congenital long QT and short QT syndromes
2009The most recent findings of Long and Short QT Syndrome are ...
Schwartz, PJ, Crotti, L
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An Overview of Congenital Long QT Syndrome
The Journal of Continuing Education in Nursing, 2005openaire +2 more sources