Sudden cardiac death without structural heart disease: update on the long QT and Brugada syndromes (Q36232414)

12 August 2017

1 reference

title

Sudden cardiac death without structural heart disease: update on the long QT and Brugada syndromes (English)

1 reference

12 August 2017

1 reference

3

Wojciech Zareba

1 reference

12 August 2017

1

Ilan Goldenberg

1 reference

12 August 2017

Arthur J Moss

2

1 reference

12 August 2017

publication date

1 September 2005

1 reference

Current cardiology reports

12 August 2017

published in

1 reference

12 August 2017

volume

7

1 reference

12 August 2017

issue

5

1 reference

12 August 2017

page(s)

349-356

1 reference

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

12 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS11886-005-0088-1

A single Na(+) channel mutation causing both long-QT and Brugada syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-005-0088-1

Diagnostic criteria for the long QT syndrome. An update

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-005-0088-1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-005-0088-1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-005-0088-1

Long-term follow-up of patients with long-QT syndrome treated with beta-blockers and continuous pacing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-005-0088-1

Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel

21 January 2018

1 reference

12 December 2020

Efficacy of quinidine in high-risk patients with Brugada syndrome

1 reference

12 December 2020

Vagal activity modulates spontaneous augmentation of ST elevation in the daily life of patients with Brugada syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic control of sodium channel function

1 reference

12 December 2020

Association of long QT syndrome loci and cardiac events among patients treated with beta-blockers.

1 reference

12 December 2020

Natural history of Brugada syndrome: insights for risk stratification and management

1 reference

12 December 2020

Biology of cardiac arrhythmias: ion channel protein trafficking

1 reference

12 December 2020

The Brugada syndrome: ionic basis and arrhythmia mechanisms

1 reference

12 December 2020

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

1 reference

12 December 2020

Implantable cardioverter defibrillator therapy in children with long QT syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Long-term follow-up of individuals with the electrocardiographic pattern of right bundle-branch block and ST-segment elevation in precordial leads V1 to V3.

1 reference

12 December 2020

Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromes

1 reference

12 December 2020

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

1 reference

12 December 2020

Novel Brugada SCN5A Mutation Leading to ST Segment Elevation in the Inferior or the Right Precordial Leads

1 reference

12 December 2020

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

1 reference

12 December 2020

Modulating effects of age and gender on the clinical course of long QT syndrome by genotype

1 reference

12 December 2020

Mapping and ablation of ventricular fibrillation associated with long-QT and Brugada syndromes

1 reference

12 December 2020

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

1 reference

12 December 2020

Left cardiac sympathetic denervation in the management of high-risk patients affected by the long-QT syndrome

1 reference

12 December 2020

Clinical and molecular heterogeneity in the Brugada syndrome: a novel gene locus on chromosome 3.

1 reference

12 December 2020

Ventricular fibrillation during anesthesia in association with J waves in the left precordial leads in a child with coarctation of the aorta

1 reference

12 December 2020

Compound mutations: a common cause of severe long-QT syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Sympathetic ganglionectomy for treatment of long-QT-interval syndrome.

1 reference

12 December 2020

Prevention of ventricular fibrillation by cilostazol, an oral phosphodiesterase inhibitor, in a patient with Brugada syndrome

1 reference

12 December 2020

Risk stratification in the long-QT syndrome.

1 reference

12 December 2020

Location of mutation in the KCNQ1 and phenotypic presentation of long QT syndrome

1 reference

12 December 2020

Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non-SCN5A-related patients

1 reference

12 December 2020

Electrophysiologic characteristics and implications of induced ventricular fibrillation in symptomatic patients with Brugada syndrome

1 reference

12 December 2020

Novel therapeutics for treatment of long-QT syndrome and torsade de pointes

1 reference

12 December 2020

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

1 reference

12 December 2020

Sodium channel gene (SCN5A) mutations in 44 index patients with Brugada syndrome: different incidences in familial and sporadic disease

1 reference

12 December 2020

Hydroquinidine therapy in Brugada syndrome

1 reference

12 December 2020

T-wave patterns associated with the hereditary long QT syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Implantable cardioverter defibrillator in high-risk long QT syndrome patients

1 reference

12 December 2020

Quinidine induced electrocardiographic normalization in two patients with Brugada syndrome

1 reference

12 December 2020

Long-term prognosis of individuals with right precordial ST-segment-elevation Brugada syndrome

1 reference

12 December 2020

Electrophysiologic investigation in Brugada syndrome; yield of programmed ventricular stimulation at two ventricular sites with up to three premature beats.

1 reference

12 December 2020

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

1 reference

12 December 2020

Pharmacological and device approach to therapy of inherited cardiac diseases associated with cardiac arrhythmias and sudden death

1 reference

12 December 2020

10.1007/S11886-005-0088-1

Identifiers

DOI

1 reference

12 August 2017

1 reference