(Q43557311)

24 November 2017

Effect of the antimalarial drug halofantrine in the long QT syndrome due to a mutation of the cardiac sodium channel gene SCN5A. (English)

1 reference

24 November 2017

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Piippo K

1

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24 November 2017

Holmström S

2

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24 November 2017

Swan H

3

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24 November 2017

Viitasalo M

4

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24 November 2017

Raatikka M

5

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24 November 2017

Toivonen L

6

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24 November 2017

Kontula K

7

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24 November 2017

language of work or name

English

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publication date

1 April 2001

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American Journal of Cardiology

24 November 2017

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24 November 2017

87

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24 November 2017

7

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24 November 2017

909-911

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The molecular genetics of the long QT syndrome: genes causing fainting and sudden death

24 November 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901538-1

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%2FS0002-9149%2800%2901538-1

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901538-1

Molecular genetics of the long QT syndrome: two novel mutations of the KVLQT1 gene and phenotypic expression of the mutant gene in a large kindred

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901538-1

Survey of the coding region of the HERG gene in long QT syndrome reveals six novel mutations and an amino acid polymorphism with possible phenotypic effects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901538-1

Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901538-1

Genomic organization of the human SCN5A gene encoding the cardiac sodium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901538-1

Provocation of ventricular tachycardia by antimalarial drug halofantrine in congenital long QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901538-1

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901538-1

Cardiac conduction defects associate with mutations in SCN5A

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901538-1

A single Na(+) channel mutation causing both long-QT and Brugada syndromes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901538-1

Activation and inactivation of the voltage-gated sodium channel: role of segment S5 revealed by a novel hyperkalaemic periodic paralysis mutation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901538-1

Clinical pharmacokinetics of halofantrine

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901538-1

Mechanism of cardiotoxicity of halofantrine

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901538-1

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901538-1

Evidence for a cardiac ion channel mutation underlying drug-induced QT prolongation and life-threatening arrhythmias

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901538-1

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%2FS0002-9149%2800%2901538-1

A common polymorphism associated with antibiotic-induced cardiac arrhythmia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901538-1

10.1016/S0002-9149(00)01538-1

7 January 2021

Identifiers

DOI

1 reference

24 November 2017

1 reference