(Q33145164)

22 July 2017

title

Jervell and Lange-Nielsen syndrome: neurologic and cardiologic evaluation (English)

1 reference

22 July 2017

Ilhan A

1

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22 July 2017

Tuncer C

series ordinal

2

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22 July 2017

Komsuoglu SS

series ordinal

3

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22 July 2017

Kali S

series ordinal

4

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22 July 2017

publication date

1 November 1999

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22 July 2017

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22 July 2017

volume

21

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22 July 2017

issue

5

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22 July 2017

page(s)

809-813

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

22 July 2017

cites work

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7 January 2021

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7 January 2021

Diagnostic criteria for the long QT syndrome. An update

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

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7 January 2021

The long Q-T syndrome

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QT dispersion: an indication of arrhythmia risk in patients with long QT intervals

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QT dispersion and sudden unexpected death in chronic heart failure

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7 January 2021

Dispersion of QT interval in patients with and without susceptibility to ventricular tachyarrhythmias after previous myocardial infarction

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7 January 2021

The role of local disparity in conduction and recovery time on ventricular vulnerability to fibrillation

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7 January 2021

Mechanism of ventricular arrhythmias caused by increased dispersion of repolarization.

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7 January 2021

Nonuniform recovery of excitability in the left ventricle

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

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7 January 2021

Mutation of the gene for IsK associated with both Jervell and Lange-Nielsen and Romano-Ward forms of Long-QT syndrome

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7 January 2021

The Jervell and Lange-Nielsen syndrome

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7 January 2021

Idiopathic long QT syndrome: asking the right question

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7 January 2021

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

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7 January 2021

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

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7 January 2021

Locus heterogeneity of autosomal dominant long QT syndrome

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7 January 2021

Evidence of genetic and phenotypic heterogeneity in the Romano-Ward syndrome

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Left cardiac sympathetic denervation in the therapy of congenital long QT syndrome. A worldwide report

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7 January 2021

Long QT syndrome: an indication for cervicothoracic sympathectomy

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7 January 2021

10.1016/S0887-8994(99)00100-9

Identifiers

DOI

1 reference

22 July 2017

1 reference