Cellular basis for electrocardiographic and arrhythmic manifestations of Andersen-Tawil syndrome (LQT7).
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Genetics of channelopathies associated with sudden cardiac deathMolecular and genetic basis of sudden cardiac deathCaMKII regulation of cardiac K channelsElectrophysiological Mechanisms of Brugada Syndrome: Insights from Pre-clinical and Clinical StudiesVentricular ectopy during REM sleep: implications for nocturnal sudden cardiac death.Risk stratification in young patients with channelopathies.Cardiac characteristics and long-term outcome in Andersen-Tawil syndrome patients related to KCNJ2 mutation.Novel mutation in the KCNJ2 gene is associated with a malignant arrhythmic phenotype of Andersen-Tawil syndrome.Diastolic intracellular calcium-membrane voltage coupling gain and postshock arrhythmias: role of purkinje fibers and triggered activity.Randomized, double-blind, placebo-controlled clinical trial of a two-day regimen of dihydroartemisinin-piperaquine for malaria prevention halted for concern over prolonged corrected QT intervalBiophysical and molecular characterization of a novel de novo KCNJ2 mutation associated with Andersen-Tawil syndrome and catecholaminergic polymorphic ventricular tachycardia mimicryManagement and treatment of Andersen-Tawil syndrome (ATS).Overview of Basic Mechanisms of Cardiac ArrhythmiaDeciphering Arrhythmia Mechanisms - Tools of the TradeWide spectrum of inhibitory effects of sertraline on cardiac ion channelsIonic, molecular, and cellular bases of QT-interval prolongation and torsade de pointes.Gene mutations in cardiac arrhythmias: a review of recent evidence in ion channelopathies.Drug-induced spatial dispersion of repolarizationProtein kinase A-dependent biophysical phenotype for V227F-KCNJ2 mutation in catecholaminergic polymorphic ventricular tachycardia.Genetics and cardiac channelopathies.Optical and electrical recordings from isolated coronary-perfused ventricular wedge preparations.Mutational consequences of aberrant ion channels in neurological disorders.Transseptal dispersion of repolarization and its role in the development of Torsade de Pointes arrhythmias.IK1 and cardiac hypoxia: after the long and short QT syndromes, what else can go wrong with the inward rectifier K+ currents?Andersen-Tawil syndrome, scarier for the doctor than for the patient? Who, when, and how to treat.Pharmacological and non-pharmacological therapy for arrhythmias in the pediatric population: EHRA and AEPC-Arrhythmia Working Group joint consensus statement.Ionic mechanisms limiting cardiac repolarization reserve in humans compared to dogs.Electrophysiological mechanisms of ventricular arrhythmias in relation to Andersen-Tawil syndrome under conditions of reduced IK1: a simulation study.Mechanisms Underlying the Actions of Antidepressant and Antipsychotic Drugs That Cause Sudden Cardiac Arrest
P2860
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P2860
Cellular basis for electrocardiographic and arrhythmic manifestations of Andersen-Tawil syndrome (LQT7).
description
2006 nî lūn-bûn
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2006 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի մարտին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Cellular basis for electrocard ...... ndersen-Tawil syndrome (LQT7).
@ast
Cellular basis for electrocard ...... ndersen-Tawil syndrome (LQT7).
@en
Cellular basis for electrocard ...... ons of Andersen-Tawil syndrome
@nl
type
label
Cellular basis for electrocard ...... ndersen-Tawil syndrome (LQT7).
@ast
Cellular basis for electrocard ...... ndersen-Tawil syndrome (LQT7).
@en
Cellular basis for electrocard ...... ons of Andersen-Tawil syndrome
@nl
prefLabel
Cellular basis for electrocard ...... ndersen-Tawil syndrome (LQT7).
@ast
Cellular basis for electrocard ...... ndersen-Tawil syndrome (LQT7).
@en
Cellular basis for electrocard ...... ons of Andersen-Tawil syndrome
@nl
P2860
P1433
P1476
Cellular basis for electrocard ...... ndersen-Tawil syndrome (LQT7).
@en
P2093
Masato Tsuboi
P2860
Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)
Function, subcellular localization and assembly of a novel mutation of KCNJ2 in Andersen's syndrome.
P304
P356
10.1016/J.HRTHM.2005.11.026
P577
2006-03-01T00:00:00Z