Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients (Q75404578)

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18 November 2019

title

Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients (English)

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18 November 2019

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9

Günter Breithardt

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18 November 2019

8

Wilhelm Haverkamp

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18 November 2019

author name string

Aimée D C Paulussen

1

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18 November 2019

Ronaldus A H J Gilissen

2

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18 November 2019

Martin Armstrong

3

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18 November 2019

Pieter A Doevendans

4

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18 November 2019

Peter Verhasselt

5

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18 November 2019

Hubert J M Smeets

6

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18 November 2019

Eric Schulze-Bahr

7

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18 November 2019

Nadine Cohen

10

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18 November 2019

Jeroen Aerssens

11

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18 November 2019

publication date

4 February 2004

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Journal of Molecular Medicine

18 November 2019

published in

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18 November 2019

volume

82

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18 November 2019

issue

3

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18 November 2019

page(s)

182-188

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https://scigraph.springernature.com/pub.10.1007/s00109-003-0522-z

18 November 2019

exact match

0 references

cites work

Low penetrance in the long-QT syndrome: clinical impact

1 reference

12 December 2020

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Exclusion of KCNE1 (IsK) as a Candidate Gene for Jervell and Lange-Nielsen Syndrome

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12 December 2020

A common polymorphism associated with antibiotic-induced cardiac arrhythmia

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Delayed repolarization (QT or QTU prolongation) and malignant ventricular arrhythmias

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

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Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome

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

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Astemizole-induced torsades de pointes in a patient with vasospastic angina

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12 December 2020

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

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Torsade de pointes with a normal QT interval associated with hypokalemia: a case report

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Blockage of the HERG human cardiac K+ channel by the gastrointestinal prokinetic agent cisapride.

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Drug-induced torsades de pointes in one patient with congenital long QT syndrome

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12 December 2020

QT prolongation and development of torsades de pointes with the concomitant administration of oral erythromycin base and quinidine.

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Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population

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

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Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.

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12 December 2020

Torsades de pointes occurring in association with terfenadine use

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12 December 2020

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

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12 December 2020

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

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12 December 2020

Torsade de pointes induced by cisapride/clarithromycin interaction

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12 December 2020

Female gender as a risk factor for torsades de pointes associated with cardiovascular drugs

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12 December 2020

Polymorphism of the gene encoding a human minimal potassium ion channel (minK)

1 reference

12 December 2020

Diagnostic criteria for the long QT syndrome. An update

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12 December 2020