(Q43595378)

25 November 2017

title

Normalization of ventricular repolarization with flecainide in long QT syndrome patients with SCN5A:DeltaKPQ mutation (English)

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25 November 2017

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Windle JR

1

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25 November 2017

Geletka RC

2

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25 November 2017

Moss AJ

3

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25 November 2017

Zareba W

4

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25 November 2017

Atkins DL

5

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25 November 2017

language of work or name

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1 April 2001

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Annals of Noninvasive Electrocardiology

25 November 2017

published in

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25 November 2017

volume

6

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25 November 2017

issue

2

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25 November 2017

page(s)

153-158

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The long QT syndrome. Prospective longitudinal study of 328 families

25 November 2017

cites work

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https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00100.X

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00100.X

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

21 January 2018

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SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00100.X

Mutations in the hminK gene cause long QT syndrome and suppress IKs function

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00100.X

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

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00100.X

Multiple mechanisms of Na+ channel--linked long-QT syndrome.

21 January 2018

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Congenital long-QT syndrome caused by a novel mutation in a conserved acidic domain of the cardiac Na+ channel.

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00100.X

Molecular mechanism for an inherited cardiac arrhythmia

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00100.X

Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00100.X

Novel LQT-3 mutation affects Na+ channel activity through interactions between alpha- and beta1-subunits

21 January 2018

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Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

21 January 2018

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Unhealthy effects of atmospheric temperature and pressure on the occurrence of myocardial infarction and coronary deaths. A 10-year survey: the Lille-World Health Organization MONICA project (Monitoring trends and determinants in cardiovascular dise

21 January 2018

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21 January 2018

Drug therapy. Flecainide

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12 December 2020

Preferential block of late sodium current in the LQT3 DeltaKPQ mutant by the class I(C) antiarrhythmic flecainide.

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12 December 2020

Mortality and morbidity in patients receiving encainide, flecainide, or placebo. The Cardiac Arrhythmia Suppression Trial

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12 December 2020

ECG T-Wave Patterns in Genetically Distinct Forms of the Hereditary Long QT Syndrome

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12 December 2020

Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene

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12 December 2020

Effects of flecainide in patients with new SCN5A mutation: mutation-specific therapy for long-QT syndrome?

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12 December 2020

A de novo missense mutation (R1623Q) of the SCN5A gene in a Japanese girl with sporadic long QT sydrome. Mutations in brief no. 140. Online

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12 December 2020

10.1111/J.1542-474X.2001.TB00100.X

Identifiers

DOI

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25 November 2017

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