The role of ion channelopathies in sudden cardiac death: implications for clinical practice (Q33162743)

23 July 2017

title

The role of ion channelopathies in sudden cardiac death: implications for clinical practice (English)

1 reference

23 July 2017

Claire A Martin

1

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23 July 2017

Christopher L-H Huang

series ordinal

2

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23 July 2017

Gareth D K Matthews

series ordinal

3

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23 July 2017

language of work or name

English

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publication date

8 May 2013

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23 July 2017

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23 July 2017

volume

45

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23 July 2017

issue

4

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23 July 2017

page(s)

364-374

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Population-based analysis of sudden cardiac death with and without left ventricular systolic dysfunction: two-year findings from the Oregon Sudden Unexpected Death Study

23 July 2017

cites work

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Epidemiology of sudden cardiac death: clinical and research implications

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Out-of-Hospital Cardiac Arrest in the 1990s: A Population-Based Study in the Maastricht Area on Incidence, Characteristics and Survival

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Sudden death in the general population in Okinawa: incidence and causes of death.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Idiopathic ventricular fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Postmortem long QT syndrome genetic testing for sudden unexplained death in the young

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Cardiac ion channel mutations in the sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

The role of molecular autopsy in unexplained sudden cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Modelling the long QT syndrome with induced pluripotent stem cells

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Dantrolene rescues arrhythmogenic RYR2 defect in a patient-specific stem cell model of catecholaminergic polymorphic ventricular tachycardia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

<i>In vitro</i> Modeling of Ryanodine Receptor 2 Dysfunction Using Human Induced Pluripotent Stem Cells

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Prevalence of the congenital long-QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

QTc Behavior During Exercise and Genetic Testing for the Long-QT Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Risk stratification in the long-QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Mouse models of long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Early afterdepolarizations: mechanism of induction and block. A role for L-type Ca2 current

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Determinants of incomplete penetrance and variable expressivity in heritable cardiac arrhythmia syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

The congenital long QT syndromes from genotype to phenotype: clinical implications

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Genetics of ion-channel disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Genetics of Sudden Cardiac Death

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Risk factors for aborted cardiac arrest and sudden cardiac death in children with the congenital long-QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Clinical course and risk stratification of patients affected with the Jervell and Lange-Nielsen syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Implantable cardioverter defibrillator in high-risk long QT syndrome patients

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Trafficking defects and gating abnormalities of a novel SCN5A mutation question gene-specific therapy in long QT syndrome type 3.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Brugada syndrome: from cell to bedside

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

The prevalence, incidence and prognostic value of the Brugada-type electrocardiogram: a population-based study of four decades

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

"Brugada" syndrome: clinical data and suggested pathophysiological mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

21 January 2018

Brugada syndrome 2012.

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na current and causes inherited arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Distribution, Splicing and Glucocorticoid-Induced Expression of Cardiacα1Candα1DVoltage-gated Ca2 Channel mRNAs

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Structure of a complex between a voltage-gated calcium channel beta-subunit and an alpha-subunit domain.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Sodium channels as macromolecular complexes: implications for inherited arrhythmia syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Loss-of-function mutation of the SCN3B-encoded sodium channel {beta}3 subunit associated with a case of idiopathic ventricular fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Functional effects of KCNE3 mutation and its role in the development of Brugada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Are women with severely symptomatic brugada syndrome different from men?

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Gender difference and drug challenge in Brugada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Cellular and ionic basis for the sex-related difference in the manifestation of the Brugada syndrome and progressive conduction disease phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Estradiol promotes sudden cardiac death in transgenic long QT type 2 rabbits while progesterone is protective

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Ventricular arrhythmia induced by sodium channel blocker in patients with Brugada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Proposed diagnostic criteria for the Brugada syndrome: consensus report

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Autonomic and antiarrhythmic drug modulation of ST segment elevation in patients with Brugada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

The genetic basis of Brugada syndrome: a mutation update

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Cellular basis for the Brugada syndrome and other mechanisms of arrhythmogenesis associated with ST-segment elevation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Paradoxic abbreviation of repolarization in epicardium of the right ventricular outflow tract during augmentation of Brugada-type ST segment elevation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Delay in right ventricular activation contributes to Brugada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Body surface area of ST elevation and the presence of late potentials correlate to the inducibility of ventricular tachyarrhythmias in Brugada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational study.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

High-density substrate mapping in Brugada syndrome: combined role of conduction and repolarization heterogeneities in arrhythmogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Repolarization heterogeneity in the right ventricular outflow tract: correlation with ventricular arrhythmias in Brugada patients and in an in vitro canine Brugada model

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Action potential alternans in the right ventricular outflow tract in a patient with asymptomatic Brugada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Brugada electrocardiographic pattern induced by fever

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

From pulsus to pulseless: the saga of cardiac alternans

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Reduced Na and higher K channel expression and function contribute to right ventricular origin of arrhythmias in Scn5a /− mice

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Mapping of reentrant spontaneous polymorphic ventricular tachycardia in a Scn5a /− mouse model

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Spatial and temporal heterogeneities are localized to the right ventricular outflow tract in a heterozygotic Scn5a mouse model

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Regional variations in action potential alternans in isolated murine Scn5a ( /-) hearts during dynamic pacing

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Impaired impulse propagation in Scn5a-knockout mice: combined contribution of excitability, connexin expression, and tissue architecture in relation to aging

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Outcome after implantation of a cardioverter-defibrillator in patients with Brugada syndrome: a multicenter study

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Efficacy of quinidine in high-risk patients with Brugada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Empiric quinidine therapy for asymptomatic Brugada syndrome: time for a prospective registry

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Drugs and Brugada syndrome patients: review of the literature, recommendations, and an up-to-date website (www.brugadadrugs.org)

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Natural history of Brugada syndrome: the prognostic value of programmed electrical stimulation of the heart

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Long-term prognosis of patients diagnosed with Brugada syndrome: Results from the FINGER Brugada Syndrome Registry

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Long-term prognosis of probands with Brugada-pattern ST-elevation in leads V1-V3.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Role of programmed ventricular stimulation in patients with Brugada syndrome: a meta-analysis of worldwide published data

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Risk stratification of individuals with the Brugada electrocardiogram: a meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Catecholaminergic polymorphic ventricular tachycardia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Targeted mutational analysis of the RyR2-encoded cardiac ryanodine receptor in sudden unexplained death: a molecular autopsy of 49 medical examiner/coroner's cases

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia: clinical features and assignment of the disease gene to chromosome 1p13-21.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Arrhythmogenic right ventricular dysplasia: a United States experience

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Ryanodine Receptor Physiology and Its Role in Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Yield of genetic screening in inherited cardiac channelopathies: how to prioritize access to genetic testing.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

A cardiac arrhythmia syndrome caused by loss of ankyrin-B function

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Enhanced store overload-induced Ca2 release and channel sensitivity to luminal Ca2 activation are common defects of RyR2 mutations linked to ventricular tachycardia and sudden death

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Sudden death in familial polymorphic ventricular tachycardia associated with calcium release channel (ryanodine receptor) leak

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

The mechanism of catecholaminergic polymorphic ventricular tachycardia may be triggered activity due to delayed afterdepolarization

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Calcium channel blockers and beta-blockers versus beta-blockers alone for preventing exercise-induced arrhythmias in catecholaminergic polymorphic ventricular tachycardia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Short QT Syndrome: a familial cause of sudden death

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Sudden death associated with short-QT syndrome linked to mutations in HERG.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Mutation in the KCNQ1 gene leading to the short QT-interval syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Short QT syndrome: pharmacological treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Early repolarization syndrome – a new electrical disorder associated with sudden cardiac death –.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Sudden cardiac arrest associated with early repolarization

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Early repolarization: electrocardiographic phenotypes associated with favorable long-term outcome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Cellular basis for the electrocardiographic J wave

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Ventricular fibrillation with prominent early repolarization associated with a rare variant of KCNJ8/KATP channel

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Electrocardiographic Characteristics and SCN5A Mutations in Idiopathic Ventricular Fibrillation Associated With Early Repolarization

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Survivors of Out-of-Hospital Cardiac Arrest With Apparently Normal Heart: Need for Definition and Standardized Clinical Evaluation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Arrhythmogenic Marker for the Sudden Unexplained Death Syndrome in Thai Men

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Haplotype-sharing analysis implicates chromosome 7q36 harboring DPP6 in familial idiopathic ventricular fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Cardiac conduction defects associate with mutations in SCN5A

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

A complex double deletion in LMNA underlies progressive cardiac conduction disease, atrial arrhythmias, and sudden death.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Familial sinus bradycardia associated with a mutation in the cardiac pacemaker channel

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Long-term follow-up of patients from a randomised trial of atrial versus ventricular pacing for sick-sinus syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

The syndrome of right bundle branch block ST segment elevation in V1 to V3 and sudden death--the Brugada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

Risk stratification in Brugada syndrome: results of the PRELUDE (PRogrammed ELectrical stimUlation preDictive valuE) registry.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109/07853890.2013.783994

10.3109/07853890.2013.783994

21 January 2018

Identifiers

DOI

1 reference

23 July 2017

1 reference