(Q37108947)

18 August 2017

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title

Molecular aspects of the congenital and acquired Long QT Syndrome: clinical implications (English)

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18 August 2017

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J B Saenen

1

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PubMed ID

18336833

18 August 2017

C J Vrints

series ordinal

2

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18 August 2017

9 February 2008

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Journal of Molecular and Cellular Cardiology

18 August 2017

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18 August 2017

44

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18 August 2017

4

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18 August 2017

633-646

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Sudden cardiac death: epidemiology, transient risk, and intervention assessment

18 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Taking the "idio" out of "idiosyncratic": predicting torsades de pointes

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

GENETICAL ASPECTS OF THE CARDIO-AUDITORY SYNDROME OF JERVELL AND LANGE-NIELSEN (CONGENITAL DEAFNESS AND ELECTROCARDIOGRAPHIC ABNORMALITIES).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Unique topographical distribution of M cells underlies reentrant mechanism of torsade de pointes in the long-QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Phase 2 early afterdepolarization as a trigger of polymorphic ventricular tachycardia in acquired long-QT syndrome : direct evidence from intracellular recordings in the intact left ventricular wall

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

The M cell: its contribution to the ECG and to normal and abnormal electrical function of the heart

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

The potential for QT prolongation and pro-arrhythmia by non-anti-arrhythmic drugs: clinical and regulatory implications. Report on a Policy Conference of the European Society of Cardiology.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

A K+ channel splice variant common in human heart lacks a C-terminal domain required for expression of rapidly activating delayed rectifier current.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Drug-induced prolongation of the QT interval

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

A single hERG mutation underlying a spectrum of acquired and congenital long QT syndrome phenotypes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Molecular physiology of cardiac repolarization

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Biology of cardiac arrhythmias: ion channel protein trafficking

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

HERG, a human inward rectifier in the voltage-gated potassium channel family

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Molecular mechanism for an inherited cardiac arrhythmia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Ankyrins and human disease: what the electrophysiologist should know

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

SCN4B-encoded sodium channel beta4 subunit in congenital long-QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Subunit interaction determines IKs participation in cardiac repolarization and repolarization reserve

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Modelling and imaging cardiac repolarization abnormalities

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Long QT syndrome: reduced repolarization reserve and the genetic link

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Cardiac IKr channels minimally comprise hERG 1a and 1b subunits

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Fast inactivation causes rectification of the IKr channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Most LQT2 mutations reduce Kv11.1 (hERG) current by a class 2 (trafficking-deficient) mechanism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

A critical role for the S4-S5 intracellular loop in domain IV of the sodium channel alpha-subunit in fast inactivation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

The congenital long QT syndromes from genotype to phenotype: clinical implications

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Highly variable mRNA expression and splicing of L-type voltage-dependent calcium channel alpha subunit 1C in human heart tissues

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Physicochemical features of the HERG channel drug binding site

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

A structural basis for drug-induced long QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Gating of shaker-type channels requires the flexibility of S6 caused by prolines

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

hERG potassium channels and cardiac arrhythmia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Pentamidine-induced long QT syndrome and block of hERG trafficking

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

A novel mutation (T65P) in the PAS domain of the human potassium channel HERG results in the long QT syndrome by trafficking deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Influence of cytochrome P450 polymorphisms on drug therapies: pharmacogenetic, pharmacoepigenetic and clinical aspects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Low penetrance in the long-QT syndrome: clinical impact

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Coordinated down-regulation of KCNQ1 and KCNE1 expression contributes to reduction of I(Ks) in canine hypertrophied hearts.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

The dominant negative LQT2 mutation A561V reduces wild-type HERG expression

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Nonsense mutations in hERG cause a decrease in mutant mRNA transcripts by nonsense-mediated mRNA decay in human long-QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Compound mutations: a common cause of severe long-QT syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Diagnostic criteria for the long QT syndrome. An update

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

ACC/AHA/ESC 2006 Guidelines for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death: a report of the American College of Cardiology/American Heart Association Task Force and the European Society of Cardiolo

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Risk of aborted cardiac arrest or sudden cardiac death during adolescence in the long-QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Long QT syndrome in adults.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Sex differences in ventricular repolarization: from cardiac electrophysiology to Torsades de Pointes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Impact of sex and gonadal steroids on prolongation of ventricular repolarization and arrhythmias induced by I(K)-blocking drugs

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Risk stratification in the long-QT syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Effectiveness and limitations of beta-blocker therapy in congenital long-QT syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Association of long QT syndrome loci and cardiac events among patients treated with beta-blockers.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Relation between QT intervals and heart rates from 40 to 120 beats/min in rest electrocardiograms of men and a simple method to adjust QT interval values.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

QT dispersion does not represent electrocardiographic interlead heterogeneity of ventricular repolarization

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

The terminal portion of the T wave: a new electrocardiographic marker of risk of ventricular arrhythmias

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Increased short-term variability of repolarization predicts d-sotalol-induced torsades de pointes in dogs

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome: ECG findings identify genotypes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Effects of a K(+) channel opener to reduce transmural dispersion of repolarization and prevent torsade de pointes in LQT1, LQT2, and LQT3 models of the long-QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

Biophysical characterization of the new human ether-a-go-go-related gene channel opener NS3623 [N-(4-bromo-2-(1H-tetrazol-5-yl)-phenyl)-N'-(3'-trifluoromethylphenyl)urea].

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2008.01.006

10.1016/J.YJMCC.2008.01.006

7 January 2021

Identifiers

DOI

1 reference

18 August 2017

1 reference

PubMed ID

18336833