(Q35791484)

10 August 2017

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title

Genetic basis of drug-induced arrhythmias (English)

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10 August 2017

Marc A Vos

1

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10 August 2017

Aimée D C Paulussen

series ordinal

2

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10 August 2017

language of work or name

English

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publication date

1 January 2004

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10 August 2017

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10 August 2017

volume

36 Suppl 1

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10 August 2017

page(s)

35-40

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Electrophysiologic parameters and predisposing factors in the generation of drug-induced Torsade de Pointes arrhythmias

10 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032634

Do we understand the electrophysiologic mechanisms responsible for drug-induced cardiac arrhythmias?

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032634

A common polymorphism associated with antibiotic-induced cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032634

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032634

Non-invasive testing of acquired long QT syndrome: evidence for multiple arrhythmogenic substrates

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032634

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032634

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032634

Torsade de pointes induced by cisapride/clarithromycin interaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032634

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032634

Drug-induced long-QT syndrome associated with a subclinical SCN5A mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032634

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032634

Sotalol testing unmasks altered repolarization in patients with suspected acquired long-QT-syndrome--a case-control pilot study using i.v. sotalol

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032634

Two linked mutations in transcriptional regulatory elements of the CYP3A5 gene constitute the major genetic determinant of polymorphic activity in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032634

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032634

Hypokalemia-induced long QT syndrome with an underlying novel missense mutation in S4-S5 linker of KCNQ1

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032634

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032634

Acquired delayed rectifier channelopathies: how heart disease and antiarrhythmic drugs mimic potentially-lethal congenital cardiac disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032634

Polymorphisms in beta-adrenergic receptor genes in the acquired long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032634

10.1080/17431380410032634

21 January 2018

Identifiers

DOI

1 reference

10 August 2017

1 reference