(Q36474145)

14 August 2017

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title

Sodium channel variants in heart disease: expanding horizons (English)

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14 August 2017

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Hanno L Tan

1

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14 August 2017

publication date

1 May 2006

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Journal of Cardiovascular Electrophysiology

14 August 2017

published in

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14 August 2017

volume

17 Suppl 1

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14 August 2017

page(s)

S151-S157

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Genetic control of sodium channel function

14 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

A calcium sensor in the sodium channel modulates cardiac excitability

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

A sodium-channel mutation causes isolated cardiac conduction disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Pharmacological rescue of mutant ion channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Abrupt rate accelerations or premature beats cause life-threatening arrhythmias in mice with long-QT3 syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Molecular mechanism for an inherited cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Cellular basis for the Brugada syndrome and other mechanisms of arrhythmogenesis associated with ST-segment elevation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Pathophysiological mechanisms of Brugada syndrome: depolarization disorder, repolarization disorder, or more?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Delay in right ventricular activation contributes to Brugada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Contribution of sodium channel mutations to bradycardia and sinus node dysfunction in LQT3 families

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Mouse model of SCN5A-linked hereditary Lenègre's disease: age-related conduction slowing and myocardial fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Sodium channel mutations and susceptibility to heart failure and atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Right bundle branch block, right precordial st-segment elevation, and sudden death in young people.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Results of ajmaline testing in patients with arrhythmogenic right ventricular dysplasia-cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Is there an overlap between Brugada syndrome and arrhythmogenic right ventricular cardiomyopathy/dysplasia?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Effects of gonadal steroids on gender-related differences in transmural dispersion of L-type calcium current

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Increased late sodium current in myocytes from a canine heart failure model and from failing human heart.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Repolarization abnormalities in cardiomyocytes of dogs with chronic heart failure: role of sustained inward current.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Lidocaine action on Na+ currents in ventricular myocytes from the epicardial border zone of the infarcted heart.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Two distinct congenital arrhythmias evoked by a multidysfunctional Na(+) channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Idiopathic ventricular fibrillation induced with vagal activity in patients without obvious heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00398.X

10.1111/J.1540-8167.2006.00398.X

21 January 2018

Identifiers

DOI

1 reference

release_kkemjuisyfgu5asrfnma7yfuaq

14 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/kkemjuisyfgu5asrfnma7yfuaq

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference