(Q33145050)

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Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome.

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1 November 2019

Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome (English)

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1 November 2019

Peter J. Schwartz

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1 November 2019

Carlo Napolitano

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1 November 2019

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A J Moss

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1 November 2019

J L Robinson

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1 November 2019

L Gessman

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1 November 2019

R Gillespie

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1 November 2019

W Zareba

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1 November 2019

G M Vincent

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1 November 2019

J Benhorin

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1 November 2019

E L Heilbron

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1 November 2019

J A Towbin

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1 November 2019

S G Priori

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1 November 2019

L Zhang

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1 November 2019

A Medina

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1 November 2019

M L Andrews

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1 November 2019

K Timothy

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1 November 2019

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1 October 1999

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1 November 2019

American Journal of Cardiology

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1 November 2019

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1 November 2019

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1 November 2019

876-879

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1 November 2019

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2899%2900458-0

7 January 2021

Ventricular Fibrillation Occurring on Arousal from Sleep by Auditory Stimuli

1 reference

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7 January 2021

The long Q-T syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2899%2900458-0

7 January 2021

The long QT syndrome in children. An international study of 287 patients

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7 January 2021

The long QT syndrome: ion channel diseases of the heart

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7 January 2021

Pathogenesis and therapy of the idiopathic long QT syndrome

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https://api.crossref.org/works/10.1016%2FS0002-9149%2899%2900458-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2899%2900458-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2899%2900458-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2899%2900458-0

7 January 2021

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

1 reference

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7 January 2021

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

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7 January 2021

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.

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2899%2900458-0

7 January 2021

The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome

1 reference

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7 January 2021

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

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7 January 2021

The long QT syndrome: a prospective international study

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7 January 2021

The long QT syndrome. Prospective longitudinal study of 328 families

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7 January 2021

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

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2899%2900458-0

7 January 2021

Molecular basis of the long-QT syndrome associated with deafness

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Identifiers

10.1016/S0002-9149(99)00458-0

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1 November 2019

PubMed publication ID

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1 November 2019

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