(Q57807332)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10735633%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

title

Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2 (English)

1 reference

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5 November 2019

1 reference

1

1 reference

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5 November 2019

Jorgen K. Kanters

4

1 reference

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5 November 2019

Paal S Andersen

5

1 reference

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5 November 2019

author name string

I H Svendsen

2

1 reference

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5 November 2019

A M Jensen

3

1 reference

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5 November 2019

M Møller

6

1 reference

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5 November 2019

S A Sørensen

7

1 reference

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5 November 2019

E Sandøe

8

1 reference

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5 November 2019

J R Jacobsen

9

1 reference

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5 November 2019

J Vuust

10

1 reference

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5 November 2019

M Christiansen

11

1 reference

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5 November 2019

publication date

1 February 2000

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5 November 2019

1 reference

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5 November 2019

volume

57

1 reference

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5 November 2019

issue

2

1 reference

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5 November 2019

page(s)

125-130

1 reference

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

5 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

Long QT syndrome-associated mutations in the Per-Arnt-Sim (PAS) domain of HERG potassium channels accelerate channel deactivation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

Novel KCNQ1 and HERG missense mutations in Dutch long-QT families

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

Multiple different missense mutations in the pore region of HERG in patients with long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

Missense mutation in the pore region of HERG causes familial long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

A family of potassium channel genes related to eag in Drosophila and mammals

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

Alteration of ionic selectivity of a K+ channel by mutation of the H5 region

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

Influence of the genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research Group.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

Genetically defined therapy of inherited long-QT syndrome. Correction of abnormal repolarization by potassium

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

7 January 2021

High-throughput single-strand conformation polymorphism analysis by automated capillary electrophoresis: Robust multiplex analysis and pattern-based identification of allelic variants

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

7 January 2021

Low penetrance in the long-QT syndrome: clinical impact

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

7 January 2021

The relationship between QTc changes and nutrition during weight loss after gastroplasty.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570206.X

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/10.1034%2FJ.1399-0004.2000.570206.X

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/10.1034%2FJ.1399-0004.2000.570206.X

7 January 2021

10.1034/J.1399-0004.2000.570206.X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10735633%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

1 reference