Epinephrine unmasks latent mutation carriers with LQT1 form of congenital long-QT syndrome. (Q44323034)

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31 October 2019

title

Epinephrine unmasks latent mutation carriers with LQT1 form of congenital long-QT syndrome (English)

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31 October 2019

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15

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Jeffrey A Towbin

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31 October 2019

author name string

Wataru Shimizu

1

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31 October 2019

Takashi Noda

2

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31 October 2019

Hiroshi Takaki

3

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31 October 2019

Takashi Kurita

4

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31 October 2019

Noritoshi Nagaya

5

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31 October 2019

Kazuhiro Satomi

6

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31 October 2019

Kazuhiro Suyama

7

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31 October 2019

Naohiko Aihara

8

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31 October 2019

Shiro Kamakura

9

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31 October 2019

Kenji Sunagawa

10

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31 October 2019

Shigeyuki Echigo

11

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31 October 2019

Kazufumi Nakamura

12

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Tohru Ohe

13

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31 October 2019

Silvia G Priori

16

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language of work or name

English

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publication date

1 February 2003

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Journal of the American College of Cardiology

31 October 2019

published in

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31 October 2019

volume

41

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issue

4

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page(s)

633-642

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

31 October 2019

cites work

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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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Molecular diagnosis of the inherited long-QT syndrome in a woman who died after near-drowning

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Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.

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Low penetrance in the long-QT syndrome: clinical impact

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Afterdepolarizations as a mechanism for the long QT syndrome: electrophysiologic studies of a case

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Gene-specific response of dynamic ventricular repolarization to sympathetic stimulation in LQT1, LQT2 and LQT3 forms of congenital long QT syndrome

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7 January 2021

Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene

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Diagnostic criteria for the long QT syndrome. An update

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Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome: ECG findings identify genotypes

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7 January 2021

The long QT syndrome. Prospective longitudinal study of 328 families

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

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7 January 2021

Evaluation of QT interval duration and dispersion and proposed clinical criteria in diagnosis of long QT syndrome in patients with a genetically uniform type of LQT1

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7 January 2021

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

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7 January 2021

Epinephrine-induced changes in serum potassium and cardiac repolarization and effects of pretreatment with propranolol and diltiazem

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7 January 2021

Hypokalemia from Beta2-Receptor Stimulation by Circulating Epinephrine

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7 January 2021

Differential effects of beta-adrenergic agonists and antagonists in LQT1, LQT2 and LQT3 models of the long QT syndrome.

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7 January 2021

Effectiveness and limitations of beta-blocker therapy in congenital long-QT syndrome.

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7 January 2021

Differential effects of beta-blockade on dispersion of repolarization in the absence and presence of sympathetic stimulation between the LQT1 and LQT2 forms of congenital long QT syndrome

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7 January 2021

Imaging dispersion of myocardial repolarization, I: comparison of body-surface and epicardial measures

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Identifiers

DOI

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31 October 2019

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