Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1). (Q33175954)

23 July 2017

title

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

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23 July 2017

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A A Wilde

1

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23 July 2017

R J Jongbloed

2

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23 July 2017

P A Doevendans

3

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23 July 2017

D R Düren

4

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23 July 2017

R N Hauer

5

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23 July 2017

I M van Langen

6

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23 July 2017

J P van Tintelen

7

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23 July 2017

H J Smeets

8

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23 July 2017

H Meyer

9

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23 July 2017

J L Geelen

10

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23 July 2017

language of work or name

English

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publication date

1 February 1999

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Journal of the American College of Cardiology

23 July 2017

published in

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23 July 2017

volume

33

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23 July 2017

issue

2

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23 July 2017

page(s)

327-332

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Ventricular Fibrillation Occurring on Arousal from Sleep by Auditory Stimuli

23 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

Epinephrine-induced ventricular premature complexes due to early afterdepolarizations and effects of verapamil and propranolol in a patient with congenital long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

Auditory stimuli as a major cause of syncope in a patient with idiopathic long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

The roles of ion channels in an inherited heart disease: molecular genetics of the long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

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.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

The long QT syndrome: a novel missense mutation in the S6 region of the KVLQT1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

Diagnostic criteria for the long QT syndrome. An update

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

Evidence of a long QT founder gene with varying phenotypic expression in South African families

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

Differential response to Na+ channel blockade, beta-adrenergic stimulation, and rapid pacing in a cellular model mimicking the SCN5A and HERG defects present in the long-QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

Sodium channel block with mexiletine is effective in reducing dispersion of repolarization and preventing torsade des pointes in LQT2 and LQT3 models of the long-QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

Mode of onset of torsade de pointes in congenital long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

A mutation in HERG associated with notched T waves in long QT syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

Early afterdepolarizations induced by isoproterenol in patients with congenital long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

Isoproterenol antagonizes prolongation of refractory period by the class III antiarrhythmic agent E-4031 in guinea pig myocytes. Mechanism of action

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

Effects of the chromanol 293B, a selective blocker of the slow, component of the delayed rectifier K+ current, on repolarization in human and guinea pig ventricular myocytes.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

Two components of the delayed rectifier K+ current in ventricular myocytes of the guinea pig type. Theoretical formulation and their role in repolarization

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

Evidence for two components of delayed rectifier K+ current in human ventricular myocytes

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2898%2900578-6

7 January 2021

10.1016/S0735-1097(98)00578-6

Identifiers

DOI

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23 July 2017

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