Keywords: سندرم طولانی QT; Sodium current; Long-QT syndrome; Antiarrhythmic drugs
مقالات ISI سندرم طولانی QT (ترجمه نشده)
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Keywords: سندرم طولانی QT; Long-QT Syndrome; GS-458967; Late Na current; Proarrhythmia;
Keywords: سندرم طولانی QT; Long-QT syndrome; Short-QT syndrome; Brugada syndrome; Catecholaminergic polymorphic ventricular tachycardia; Ventricular fibrillation;
Effect of age and gender on the QTc-interval in healthy individuals and patients with long-QT syndrome
Keywords: سندرم طولانی QT; Electrocardiogram (ECG); Age; Gender; long-QT syndrome;
Landiolol suppression of electrical storm of torsades de pointes in patients with congenital long-QT syndrome type 2 and myocardial ischemia
Keywords: سندرم طولانی QT; Torsade de pointes; Long-QT syndrome; β-blocker; Landiolol;
Considerations when using next-generation sequencing for genetic diagnosis of long-QT syndrome in the clinical testing laboratory
Keywords: سندرم طولانی QT; Long-QT syndrome; Romano-Ward syndrome; Jervell-Lange Nielsen syndrome; High-throughput nucleotide sequencing;
Convergence of models of human ventricular myocyte electrophysiology after global optimization to recapitulate clinical long QT phenotypes
Keywords: سندرم طولانی QT; LQTS; long-QT syndrome; VM; ventricular myocyte; APD; Action potential duration; IKr; rapidly activating delayed rectifier current; IKs; slowly activating delayed rectifier current; INaL; late (persistent) sodium current; ICaL; L-type calcium current; NCX
In silico screening of the impact of hERG channel kinetic abnormalities on channel block and susceptibility to acquired long QT syndrome
Keywords: سندرم طولانی QT; aLQTS; drug-induced or acquired long-QT syndrome; AP; action potential; APD; action potential duration; APD90; action potential duration at 90% repolarization; C1; closed state 1; C2; closed state 2; C3; closed state 3; EAD; early-afterdepolarization; ECG
Calmodulin mutations associated with long QT syndrome prevent inactivation of cardiac L-type Ca2Â + currents and promote proarrhythmic behavior in ventricular myocytes
Keywords: سندرم طولانی QT; CaM; calmodulin; CPVT; catecholaminergic polymorphic ventricular tachycardia; LQT(S); long-QT (syndrome); aGPVM(s); adult guinea-pig ventricular myocyte(s); LTCC(s); L-type Ca2Â + channels; apoCaM; Ca2Â +-free calmodulin; APD; action potential duration; C
KCNE2 modulates cardiac L-type Ca2Â + channel
Keywords: سندرم طولانی QT; LCC; L-type Ca2 + channel; LQT; long-QT syndrome; ICa,L; L-type Ca2 + current; AF; atrial fibrillation; NTI; N-terminal inhibitory module; KCNE2; L-type  Ca2+ current; Cav1.2; KCNE2 mutation; Familial atrial fibrillation;
In silico screening of the impact of hERG channel kinetic abnormalities on channel block and susceptibility to acquired long QT syndrome
Keywords: سندرم طولانی QT; aLQTS; drug-induced or acquired long-QT syndrome; AP; action potential; APD; action potential duration; APD90; action potential duration at 90% repolarization; C1; closed state 1; C2; closed state 2; C3; closed state 3; EAD; early-afterdepolarization; ECG
Distinguishing Cardiac Syncope from Vasovagal Syncope in a Referral Population
Keywords: سندرم طولانی QT; CPR; Cardiopulmonary resuscitation; CPVT; Catecholaminergic polymorphic ventricular tachycardia; ECG; Electrocardiogram; ED; Emergency department; ICD-9; International Classification of Diseases, 9thRevision; LQTS; Long-QT syndrome; SCD; Sudden cardiac de
Microvolt-level T-wave alternans determination using the spectral method in patients with QT prolongation: value of adjusting the T-wave window
Keywords: سندرم طولانی QT; T-wave alternans; Spectral method; QT prolongation; Long-QT syndrome; Sudden cardiac death;
Arrhythmia formation in subclinical (“silent”) long QT syndrome requires multiple insults: Quantitative mechanistic study using the KCNQ1 mutation Q357R as example
Keywords: سندرم طولانی QT; Action potential; β-Adrenergic stimulation; Computational models; Electrophysiology; Isoproterenol; Long-QT syndrome; Repolarization reserve; Silent mutationAP, action potential; APD, action potential duration; CL, cycle length; EAD, early afterdepolariza
Developmentally regulated SCN5A splice variant potentiates dysfunction of a novel mutation associated with severe fetal arrhythmia
Keywords: سندرم طولانی QT; Arrhythmia; Sodium channel; SCN5A; Sudden death; Long-QT syndrome; Magnetocardiography; Alternative splicingAV, atrioventricular; LQTS, long-QT syndrome; TdP, torsades de pointes; WT, wild type
Trigger-specific ion-channel mechanisms, risk factors, and response to therapy in type 1 long QT syndrome
Keywords: سندرم طولانی QT; Long-QT syndrome; Sudden cardiac death; TriggersACA, aborted cardiac arrest; C-loops, cytoplasmic loops; ECG, electrocardiogram; LQTS, long-QT syndrome; LQT1, long-QT syndrome type 1; LQT2, long-QT syndrome type 2; QTc, corrected QT interval; SCD, sudden
Arrhythmogenic mechano-electric heterogeneity in the long-QT syndrome
Keywords: سندرم طولانی QT; Long-QT syndrome; Electromechanical window; Calcium; Aftercontractions; Torsades de pointes; Ventricular arrhythmia; AP; action potential; APD; action-potential duration; CaMKII; Ca2+/Calmodulin-dependent serine-threonine protein kinase II; CaM; Ca2+/Calm
A KCR1 variant implicated in susceptibility to the long QT syndrome
Keywords: سندرم طولانی QT; Ion channels; Long-QT syndrome; Drugs; Electrophysiology; Hypokalemia;
Risk for Life-Threatening Cardiac Events in Patients With Genotype-Confirmed Long-QT Syndrome and Normal-Range Corrected QT Intervals
Keywords: سندرم طولانی QT; corrected QT interval; long-QT syndrome; sudden cardiac deathACA, aborted cardiac arrest; ECG, electrocardiographic; LQTS, long-QT syndrome; LQT1, long-QT syndrome type 1; LQT2, long-QT syndrome type 2; LQT3, long-QT syndrome type 3; QTc, corrected QT int
Genetic analysis of Brugada syndrome and congenital long-QT syndrome type 3 in the Chinese
Keywords: سندرم طولانی QT; Brugada syndrome; cardiac sodium channel; long-QT syndrome; SCN5A gene mutation;
AHA/ACCF/HRS Recommendations for the Standardization and Interpretation of the Electrocardiogram
Keywords: سندرم طولانی QT; ACCF Expert Consensus Documents; electrocardiography; electrophysiology; ion channels; long-QT syndrome;
A mutation in the sodium channel is responsible for the association of long QT syndrome and familial atrial fibrillation
Keywords: سندرم طولانی QT; Long-QT syndrome; Atrial fibrillation; Genetics; Sodium channel; Channelopathies;
The canine model with chronic, complete atrio-ventricular block
Keywords: سندرم طولانی QT; AV; Atrio-ventricular; AAVB; Acute complete atrio-ventricular block; BVR; Beat-to-beat variability of repolarization; CAVB; Chronic complete atrio-ventricular block; CAVBr; CAVB resistant to drug-induced TdP; CAVBs; CAVB susceptible to drug-induced TdP; D