Cellular basis for long QT, transmural dispersion of repolarization, and torsade de pointes in the long QT syndrome (Q33845825)

29 July 2017

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title

Cellular basis for long QT, transmural dispersion of repolarization, and torsade de pointes in the long QT syndrome (English)

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29 July 2017

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2

Antzelevitch C

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29 July 2017

Shimizu W

1

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29 July 2017

1 January 1999

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Journal of Electrocardiology

29 July 2017

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29 July 2017

32 Suppl

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29 July 2017

177-184

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29 July 2017

The long Q-T syndrome

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https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

The long QT syndrome: a prospective international study

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

Early afterdepolarizations induced by isoproterenol in patients with congenital long QT syndrome

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https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

Diagnostic criteria for the long QT syndrome. An update

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

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

7 January 2021

1 reference

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Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

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

7 January 2021

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Molecular basis of the long-QT syndrome associated with deafness.

7 January 2021

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

7 January 2021

1 reference

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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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

Cellular basis for the ECG features of the LQT1 form of the long-QT syndrome: effects of beta-adrenergic agonists and antagonists and sodium channel blockers on transmural dispersion of repolarization and torsade de pointes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

Cellular basis for the normal T wave and the electrocardiographic manifestations of the long-QT syndrome

7 January 2021

1 reference

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Cellular and ionic basis for T-wave alternans under long-QT conditions

7 January 2021

1 reference

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Sodium pentobarbital reduces transmural dispersion of repolarization and prevents torsades de Pointes in models of acquired and congenital long QT syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

ECG T-Wave Patterns in Genetically Distinct Forms of the Hereditary Long QT Syndrome

7 January 2021

1 reference

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Heterogeneity within the ventricular wall. Electrophysiology and pharmacology of epicardial, endocardial, and M cells

7 January 2021

1 reference

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Clinical relevance of cardiac arrhythmias generated by afterdepolarizations. Role of M cells in the generation of U waves, triggered activity and torsade de pointes.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

The M cell: its contribution to the ECG and to normal and abnormal electrical function of the heart

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

Effects of verapamil and propranolol on early afterdepolarizations and ventricular arrhythmias induced by epinephrine in congenital long QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

Improvement of repolarization abnormalities by a K+ channel opener in the LQT1 form of congenital long-QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

Reproducible induction of early afterdepolarizations and torsade de pointes arrhythmias by d-sotalol and pacing in dogs with chronic atrioventricular block.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

The electrophysiological mechanism of ventricular arrhythmias in the long QT syndrome. Tridimensional mapping of activation and recovery patterns

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

Efficacy of permanent pacing in the management of high-risk patients with long QT syndrome

7 January 2021

1 reference

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Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

Frequency-dependent electrophysiologic properties of ventricular repolarization in patients with congenital long QT syndrome

7 January 2021

1 reference

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Mode of onset of torsade de pointes in congenital long QT syndrome

7 January 2021

1 reference

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The long QT syndrome. Prospective longitudinal study of 328 families

7 January 2021

1 reference

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-0736%2899%2990077-8

10.1016/S0022-0736(99)90077-8

7 January 2021

Identifiers

DOI

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29 July 2017

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PubMed ID

10688323