Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy (Q33156860)

22 July 2017

title

Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy (English)

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22 July 2017

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A A M Wilde

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22 July 2017

J N Johnson

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22 July 2017

N Hofman

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22 July 2017

C M Haglund

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22 July 2017

G D Cascino

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22 July 2017

M J Ackerman

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22 July 2017

language of work or name

English

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publication date

26 November 2008

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22 July 2017

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22 July 2017

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22 July 2017

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22 July 2017

page(s)

224-231

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Long QT syndrome and pregnancy

22 July 2017

cites work

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21 June 2018

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Genotype-phenotype relationships in congenital long QT syndrome

21 June 2018

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Identification of a common genetic substrate underlying postpartum cardiac events in congenital long QT syndrome

21 June 2018

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21 June 2018

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21 June 2018

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RARE CARDIAC ARRYTHMIAS OF THE PEDIATRIC AGE. II. SYNCOPAL ATTACKS DUE TO PAROXYSMAL VENTRICULAR FIBRILLATION. (PRESENTATION OF 1ST CASE IN ITALIAN PEDIATRIC LITERATURE)

21 June 2018

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A NEW FAMILIAL CARDIAC SYNDROME IN CHILDREN

21 June 2018

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

21 June 2018

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Phenytoin and phenobarbital inhibit human HERG potassium channels

21 June 2018

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Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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The inherited long QT syndrome: from ion channel to bedside

21 June 2018

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Tripartite synapses: glia, the unacknowledged partner

21 June 2018

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

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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

21 June 2018

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21 June 2018

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21 June 2018

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The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome

31 October 2018

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31 October 2018

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31 October 2018

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Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing

31 October 2018

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12 December 2020

Genotype-specific onset of arrhythmias in congenital long-QT syndrome: possible therapy implications

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12 December 2020

The congenital long QT syndrome. An unusual cause of childhood seizures

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12 December 2020

Clinical aspects of the idiopathic long QT syndrome

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12 December 2020

10.1212/01.WNL.0000335760.02995.CA

Identifiers

DOI

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22 July 2017

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22 July 2017

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