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Lista de obras de Arthur Wilde

"J-wave syndromes" bring the ATP-sensitive potassium channel back in the spotlight

artículo científico publicado en 2012

'Brugada ECG' elicited by imipramine overdose

artículo científico publicado en 2004

'Cardiac Radioablation - a Systematic Review'

scientific article published on 20 March 2020

2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy

scientific article published on 09 May 2019

2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy: Executive summary

scientific article published on 01 November 2019

2020 APHRS/HRS Expert Consensus Statement on the Investigation of Decedents with Sudden Unexplained Death and Patients with Sudden Cardiac Arrest, and of Their Families

artículo científico publicado en 2020

50 Years of Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) - Time to Explore the Dark Side of the Moon

scientific article published on 06 December 2019

A Comprehensive Evaluation of the Genetic Architecture of Sudden Cardiac Arrest

A Novel Familial Cardiac Arrhythmia Syndrome with Widespread ST-Segment Depression

artículo científico publicado en 2018

A Potential Diagnostic Approach for Foetal Long-QT Syndrome, Developed and Validated in Children

A calcium sensor in the sodium channel modulates cardiac excitability

artículo científico publicado en 2002

A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill

artículo científico publicado en 2003

A common arrhythmia, not so common at an old age.

artículo científico

A common arrhythmia, not so common at an old age.

artículo científico publicado en 2014

A common co-morbidity modulates disease expression and treatment efficacy in inherited cardiac sodium channelopathy

artículo científico publicado en 2018

A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization

artículo científico publicado en 2003

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

artículo científico publicado en 2011

A connexin40 mutation associated with a malignant variant of progressive familial heart block type I

artículo científico publicado en 2012

A fainting lady with some extrasystoles

artículo científico publicado en 2004

A family with Andersen-Tawil syndrome and dilated cardiomyopathy

scientific article published on 21 July 2006

A gain-of-function TBX5 mutation is associated with atypical Holt-Oram syndrome and paroxysmal atrial fibrillation

artículo científico publicado en 2008

A highly specific biomarker for Brugada syndrome. Also too good to be true?

artículo científico publicado en 2020

A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes

artículo científico publicado en 2011

A large family characterised by nocturnal sudden death

artículo científico publicado en 2002

A long RP supraventricular tachycardia

artículo científico publicado en 2003

A mutation in CALM1 encoding calmodulin in familial idiopathic ventricular fibrillation in childhood and adolescence

artículo científico publicado en 2013

A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families

artículo científico publicado en 2005

A narrow QRS complex tachycardia sensitive to Isoptin

artículo científico publicado en 2006

A new prediction model for ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy.

artículo científico publicado en 2019

A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kinetics

artículo científico publicado en 2003

A novel alpha-tropomyosin mutation associates with dilated and non-compaction cardiomyopathy and diminishes actin binding

artículo científico publicado en 2012

A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9q ⬇️

artículo científico publicado el 9 de marzo de 2011

A novel early onset lethal form of catecholaminergic polymorphic ventricular tachycardia maps to chromosome 7p14-p22

A novel tool to evaluate the implant position and predict defibrillation success of the subcutaneous implantable defibrillator: the PRAETORIAN score

artículo científico publicado en 2018

A pre-excited wide QRS complex: is that all there is?

artículo científico publicado en 2006

ABSTRACTS

scholarly article

Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia

artículo científico publicado en 2002

Accelerated sinus rhythm prevents catecholaminergic polymorphic ventricular tachycardia in mice and in patients.

artículo científico publicado en 2013

Accurate electrocardiographic assessment of the QT interval: teach the tangent

scientific article published on 01 April 2008

Activated human platelet products induce proarrhythmic effects in ventricular myocytes

artículo científico publicado en 2011

Activation delay and VT parameters in arrhythmogenic right ventricular dysplasia/cardiomyopathy: toward improvement of diagnostic ECG criteria

scientific article published on 26 March 2008

Active cascade screening in primary inherited arrhythmia syndromes: does it lead to prophylactic treatment?

artículo científico publicado en 2010

Acute and 3-Month Performance of a Communicating Leadless Antitachycardia Pacemaker and Subcutaneous Implantable Defibrillator

artículo científico publicado en 2017

Age of First Arrhythmic Event in Brugada Syndrome: Data From the SABRUS (Survey on Arrhythmic Events in Brugada Syndrome) in 678 Patients

artículo científico publicado en 2017

Aging in Brugada Syndrome: What About Risks?

artículo científico publicado en 2016

An International External Validation Study of the 2014 European Society of Cardiology Guideline on Sudden Cardiac Death Prevention in Hypertrophic Cardiomyopathy (Evidence from HCM).

artículo científico publicado en 2017

An International Multi-Center Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of CASQ2- Catecholaminergic Polymorphic Ventricular Tachycardia

artículo científico publicado en 2020

An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition

scientific article published on 16 January 2020

An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome

artículo científico publicado en 2020

An atypical arrhythmia

An atypical arrhythmia.

artículo científico publicado en 2013

An extended family suddenly confronted with a life-threatening hereditary arrhythmia

artículo científico publicado en 2005

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

artículo científico publicado en 2009

An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome

artículo científico publicado en 2008

An old lady with chest pain

artículo científico publicado en 2006

An unexpected ECG finding

Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2

artículo científico publicado en 2015

And what about the ECG?

artículo científico publicado en 2006

Andersen-Tawil syndrome, scarier for the doctor than for the patient? Who, when, and how to treat

artículo científico publicado en 2013

Anti-arrhythmic potential of the late sodium current inhibitor GS-458967 in murine Scn5a-1798insD+/- and human SCN5A-1795insD+/- iPSC-derived cardiomyocytes.

artículo científico publicado en 2017

Antiarrhythmic drugs, patients, and the pharmaceutical industry: value for patients, physicians, pharmacists or shareholders?

artículo científico publicado en 2007

Are women with severely symptomatic brugada syndrome different from men?

artículo científico publicado en 2008

Arrhythmias in Brugada syndrome: changing throughout day and season?

scientific article published on 03 September 2008

Arrhythmogenic right ventricular cardiomyopathy due to a novel plakophilin 2 mutation: wide spectrum of disease in mutation carriers within a family

artículo científico publicado en 2006

Arrhythmogenic right ventricular cardiomyopathy: asymptomatic to life threatening as illustrated by the cases of two sisters

artículo científico publicado en 2007

Arrhythmogenic right ventricular dysplasia/cardiomyopathy according to revised 2010 task force criteria with inclusion of non-desmosomal phospholamban mutation carriers

artículo científico publicado en 2013

Arrhythmogenic right ventricular dysplasia/cardiomyopathy diagnostic task force criteria: impact of new task force criteria

artículo científico publicado en 2010

Arrhythmogenic right ventricular dysplasia/cardiomyopathy: pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right ventricular dysplasia/cardiomyopathy genotype-phenotype follow-up study

artículo científico publicado en 2011

Assessment and Validation of a Phenotype-Enhanced Variant Classification Framework to Promote or Demote RYR2 Missense Variants of Uncertain Significance

artículo científico publicado en 2019

Assessment of the Extravascular Implantable Defibrillator: Feasibility of Substernal Ventricular Pacing

artículo científico publicado en 2017

Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events

artículo científico publicado en 2019

Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction.

artículo científico publicado en 2015

Athletes with channelopathy may be eligible to play

artículo científico publicado en 2018

Atlas of the clinical genetics of human dilated cardiomyopathy

artículo científico publicado en 2015

Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia.

artículo científico publicado en 2017

Baseline NT-ProBNP level predicts success of cardioversion of atrial fibrillation with flecainide

artículo científico publicado en 2015

Beta-blockers in the treatment of congenital long QT syndrome: is one beta-blocker superior to another?

artículo científico publicado en 2014

Biomarkers in inherited arrhythmias: necessity for validation and collaboration

artículo científico publicado en 2020

Bringing home the bacon? The next step in cardiac sodium channelopathies

artículo científico publicado en 2014

Brugada Syndrome

article from 2012

Brugada Syndrome and the Subcutaneous Implantable Cardioverter-Defibrillator

scientific article published on 01 August 2016

Brugada Syndrome: Overview

Brugada phenocopy: new terminology and proposed classification.

artículo científico

Brugada syndrome and the use of anesthetics.

artículo científico publicado en 2006

Brugada syndrome: in search of a genotype-phenotype relationship

artículo científico publicado en 2002

Brugada syndrome: report of the second consensus conference.

artículo científico publicado en 2005

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

artículo científico publicado en 2005

COMPANION - a friend indeed

artículo científico publicado en 2003

COVID-19 vaccination in patients with long QT syndrome

artículo científico publicado en 2022

Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry

scientific article published on 01 September 2019

Can parents adjust to the idea that their child is at risk for a sudden death?: Psychological impact of risk for long QT syndrome

scientific article published on 01 October 2005

Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy

artículo científico publicado en 2011

Cardiac dysfunction after aneurysmal subarachnoid hemorrhage: relationship with outcome.

artículo científico publicado en 2013

Cardiac involvement in Dutch patients with sarcoglycanopathy: a cross-sectional cohort and follow-up study

artículo científico publicado en 2014

Cardiac ion channels in health and disease

scientific article published on 05 August 2009

Cardiac resynchronization improves microcirculation

artículo científico publicado en 2007

Cardiac sodium channel overlap syndromes: different faces of SCN5A mutations

artículo científico publicado en 2008

Cardiac sodium channels and inherited electrophysiologic disorders: a pharmacogenetic overview

artículo científico publicado en 2008

Cardiogenetic counselling in a non-university hospital

artículo científico publicado en 2007

Cardiogenetics, 25 years a growing subspecialism

artículo científico publicado en 2020

Cardiomyocytes derived from pluripotent stem cells recapitulate electrophysiological characteristics of an overlap syndrome of cardiac sodium channel disease

artículo científico publicado en 2012

Cardiorenal axis and arrhythmias: Will renal sympathetic denervation provide additive value to the therapeutic arsenal?

artículo científico publicado en 2015

Cardiovascular Safety of Degarelix: Results From a 12-Month, Comparative, Randomized, Open Label, Parallel Group Phase III Trial in Patients With Prostate Cancer ⬇️

artículo científico publicado el 16 de octubre de 2010

Caring for the pregnant woman with an inherited arrhythmia syndrome

scientific article published on 07 August 2019

Carotid sinus clues

artículo científico publicado en 2003

Carriers of the hypertrophic cardiomyopathy MYBPC3 mutation are characterized by reduced myocardial efficiency in the absence of hypertrophy and microvascular dysfunction

artículo científico publicado en 2011

Cases in Precision Medicine: Genetic Assessment After a Sudden Cardiac Death in the Family

scientific article published on 14 May 2019

Catecholaminergic polymorphic ventricular tachycardia: disease with different faces

artículo científico publicado en 2015

Catecholaminergic polymorphic ventricular tachycardia: from bench to bedside

artículo científico publicado en 2013

Catecholaminergic polymorphic ventricular tachycardia: important messages from case reports ⬇️

artículo científico publicado el 17 de septiembre de 2010

Catecholaminergic polymorphic ventricular tachycardia; possible diagnosis in cases of syncope and sudden death of family members

artículo científico publicado en 2015

Catheter ablation in highly symptomatic Brugada patients: a Dutch case series

scientific article published on 02 September 2019

Challenging the unifying pathophysiological concept of J-wave syndromes.

artículo científico publicado en 2016

Channelopathies as Causes of Sudden Cardiac Death

artículo científico publicado en 2017

Channelopathies in children and adults

artículo científico publicado en 2008

Channelopathies, genetic testing and risk stratification

artículo científico publicado en 2017

Characterization and Management of Arrhythmic Events in Young Patients With Brugada Syndrome

scientific article published on 01 April 2019

Characterization of SEMA3A-encoded semaphorin as a naturally occurring Kv4.3 protein inhibitor and its contribution to Brugada syndrome

artículo científico publicado en 2014

Characterization of a novel SCN5A mutation associated with Brugada syndrome reveals involvement of DIIIS4-S5 linker in slow inactivation

artículo científico publicado en 2007

Chemokine ligand 9 modulates cardiac repolarization via Cxcr3 receptor binding

artículo científico publicado en 2015

Chronic performance of a leadless cardiac pacemaker: 1-year follow-up of the LEADLESS trial

artículo científico publicado en 2015

Classification and Reporting of Potentially Proarrhythmic Common Genetic Variation in Long QT Syndrome Genetic Testing.

artículo científico publicado en 2018

Clinical Aspects of Type 3 Long-QT Syndrome: An International Multicenter Study

artículo científico publicado en 2016

Clinical Assessment of the Pathogenicity of Unknown Variants in Long-QT Syndrome: Does the Pendulum Swing Back?

scientific article published on 04 April 2012

Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia: The Role of Left Cardiac Sympathetic Denervation.

artículo científico publicado en 2015

Clinical and genetic analysis of long QT syndrome in children from six families in Saudi Arabia: are they different?

artículo científico publicado en 2009

Clinical and genetic characterization of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy caused by a plakophilin-2 splice mutation

artículo científico publicado en 2012

Clinical aspects and prognosis of Brugada syndrome in children

artículo científico publicado en 2007

Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene

artículo científico publicado en 2007

Clinical utility gene card for: long-QT syndrome (types 1-13).

artículo científico publicado en 2013

Clinical parameters to optimize patient selection for subcutaneous and transvenous implantable defibrillator therapy

artículo científico publicado en 2018

Combined assessment of sex- and mutation-specific information for risk stratification in type 1 long QT syndrome

artículo científico publicado en 2012

Combined leadless pacemaker and subcutaneous implantable defibrillator therapy: feasibility, safety, and performance

artículo científico publicado en 2016

Common sodium channel promoter haplotype in asian subjects underlies variability in cardiac conduction.

artículo científico publicado en 2006

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

artículo científico publicado en 2013

Communicating Antitachycardia Pacing-Enabled Leadless Pacemaker and Subcutaneous Implantable Defibrillator

artículo científico publicado en 2016

Comparison of complications and shocks in paediatric and young transvenous and subcutaneous implantable cardioverter-defibrillator patients

artículo científico publicado en 2018

Complex inheritance for susceptibility to sudden cardiac death.

artículo científico publicado en 2013

Complications related to elective generator replacement of the subcutaneous implantable defibrillator

artículo científico publicado en 2020

Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system

artículo científico publicado en 2003

Computer versus Cardiologist: Is a machine learning algorithm able to outperform an expert in diagnosing phospholamban (PLN) p.Arg14del mutation on ECG?

scientific article published on 07 September 2020

Con: Newborn screening to prevent sudden cardiac death?

artículo científico publicado en 2006

Congenital Long QT Syndrome: An Update and Present Perspective in Saudi Arabia

artículo científico publicado en 2013

Continued misuse of orphan drug legislation: a life-threatening risk for mexiletine

scientific article published on 01 February 2020

Contribution of inherited heart disease to sudden cardiac death in childhood.

artículo científico publicado en 2007

Contribution of sodium channel mutations to bradycardia and sinus node dysfunction in LQT3 families

artículo científico publicado en 2003

Corrigendum to: 'HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies' [Europace 2011;13:1077-109, doi: 10.1093/europace/eur245]

artículo científico publicado en 2012

Cost-effectiveness of genotyping in inherited arrhythmia syndromes: are we getting value for the money?

artículo científico publicado en 2009

Coxsackie and adenovirus receptor is a modifier of cardiac conduction and arrhythmia vulnerability in the setting of myocardial ischemia

artículo científico publicado en 2014

Creating certainty out of uncertainty

scientific article published on 01 March 2019

Delay in right ventricular activation contributes to Brugada syndrome

artículo científico publicado en 2004

Desmin mutations as a cause of right ventricular heart failure affect the intercalated disks

artículo científico publicado en 2010

Desmoglein-2 and desmocollin-2 mutations in dutch arrhythmogenic right ventricular dysplasia/cardiomypathy patients: results from a multicenter study

scientific article published on 01 August 2009

Desmosomal mutations across the fence

artículo científico publicado en 2011

Detailed characterization of familial idiopathic ventricular fibrillation linked to the DPP6 locus

artículo científico publicado en 2015

Determination and Interpretation of the QT Interval

scientific article published on 01 November 2018

Developmental aspects of long QT syndrome type 3 and Brugada syndrome on the basis of a single SCN5A mutation in childhood

scientific article published on 01 July 2005

Device orientation of a leadless pacemaker and subcutaneous implantable cardioverter-defibrillator in canine and human subjects and the effect on intrabody communication

scientific article published on 01 November 2018

Diagnostic Performance of Various QTc Interval Formulas in a Large Family with Long QT Syndrome Type 3: Bazett's Formula Not So Bad After All … ⬇️

artículo científico publicado el 1 de octubre de 2003

Diagnostic and genetic aspects of the Brugada and other inherited arrhythmias syndromes.

artículo científico publicado en 2007

Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?

article

Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?

artículo científico publicado en 2007

Diagnostic value of T-wave morphology changes during "QT stretching" in patients with long QT syndrome.

artículo científico publicado en 2015

Diagnostic value of flecainide testing in unmasking SCN5A-related Brugada syndrome

artículo científico publicado en 2006

Diagnostic yield in sudden unexplained death and aborted cardiac arrest in the young: the experience of a tertiary referral center in The Netherlands

artículo científico publicado en 2010

Dilation of the Aorta Ascendens Forms Part of the Clinical Spectrum of HCN4 Mutations

scientific article published on 01 May 2016

Direct comparison of a contractility and activity pacemaker sensor during treadmill exercise testing

artículo científico publicado en 2004

Disparate response of high-frequency ganglionic plexus stimulation on sinus node function and atrial propagation in patients with atrial fibrillation

artículo científico publicado en 2014

Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noise.

artículo científico publicado en 2011

Diurnal variation of ventricular repolarization in a large family with LQT3-Brugada syndrome characterized by nocturnal sudden death

artículo científico publicado en 2006

Diversity in cardiac sodium channel disease phenotype in transgenic mice carrying a single SCN5A mutation.

artículo científico publicado en 2007

Do J waves constitute a syndrome?

artículo científico publicado en 2013

Do patients with long QT syndrome remain at risk for sudden cardiac death after 40 years of age?

artículo científico publicado en 2008

Documented atrial fibrillation recurrences after pulmonary vein isolation are associated with diminished quality of life

artículo científico publicado en 2015

Does flecainide regain its antiarrhythmic activity after electrical cardioversion of persistent atrial fibrillation?

artículo científico publicado en 2005

Double trouble, stick to the basics should be the rule!

artículo científico publicado en 2014

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

artículo científico publicado en 2009

Dual inheritance of sudden death from cardiovascular causes

artículo científico publicado en 2008

Dutch outcome in implantable cardioverter-defibrillator therapy (DO-IT): registry design and baseline characteristics of a prospective observational cohort study to predict appropriate indication for implantable cardioverter-defibrillator

artículo científico

ECG quantification of myocardial scar does not differ between primary and secondary prevention ICD recipients with ischemic heart disease

artículo científico publicado en 2009

ECG screening of newborns to avoid sudden infant death syndrome?

artículo científico publicado en 2006

EP testing does not predict cardiac events in Brugada syndrome

artículo científico publicado en 2011

ESC guidance for the diagnosis and management of cardiovascular disease during the COVID-19 pandemic: part 2—care pathways, treatment, and follow-up

artículo científico publicado en 2021

Early Mechanical Alterations in Phospholamban Mutation Carriers: Identifying Subclinical Disease Before Onset of Symptoms

artículo científico publicado en 2020

Early mortality in prophylactic implantable cardioverter-defibrillator recipients: development and validation of a clinical risk score

artículo científico publicado en 2013

Effect of Age and Sex on the QTc Interval in Children and Adolescents With Type 1 and 2 Long-QT Syndrome

artículo científico publicado en 2017

Effect of Ascertainment Bias on Estimates of Patient Mortality in Inherited Cardiac Diseases

article

Effect of age and gender on the QTc-interval in healthy individuals and patients with long-QT syndrome

artículo científico publicado en 2017

Effects of flecainide on exercise-induced ventricular arrhythmias and recurrences in genotype-negative patients with catecholaminergic polymorphic ventricular tachycardia.

artículo científico publicado en 2012

Efficacy of an implantable cardioverter-defibrillator in a neonate with LQT3 associated arrhythmias

artículo científico publicado en 2005

Electrocardiographic P wave changes after thoracoscopic pulmonary vein isolation for atrial fibrillation.

artículo científico publicado en 2013

Electrocardiographic factors playing a role in ischemic ventricular fibrillation in ST elevation myocardial infarction are related to the culprit artery

artículo científico publicado en 2007

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

artículo científico publicado en 2008

Enhancing the Predictive Power of Mutations in the C-Terminus of the KCNQ1-Encoded Kv7.1 Voltage-Gated Potassium Channel

artículo científico publicado en 2015

Epicardial Substrate Ablation in Brugada Syndrome: Time for a Randomized Trial!

scientific article published on 01 December 2015

Epicardial and endocardial electrophysiological guided thoracoscopic surgery for atrial fibrillation: a multidisciplinary approach of atrial fibrillation ablation in challenging patients

artículo científico publicado en 2014

Epidemiologic, molecular, and functional evidence suggest A572D-SCN5A should not be considered an independent LQT3-susceptibility mutation.

artículo científico publicado en 2010

Epidemiology of inherited arrhythmias

scientific article published on 03 October 2019

Ethnic differences in patients with Brugada syndrome and arrhythmic events: New insights from Survey on Arrhythmic Events in Brugada Syndrome

artículo científico publicado en 2019

European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) expert consensus on risk assessment in cardiac arrhythmias: use the right tool for the right out

artículo científico publicado en 2020

European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death

article published in 2019

Evaluation of the Impact of a Chronic Total Coronary Occlusion on Ventricular Arrhythmias and Long-Term Mortality in Patients With Ischemic Cardiomyopathy and an Implantable Cardioverter-Defibrillator (the eCTOpy-in-ICD Study).

artículo científico publicado en 2018

Everybody has Brugada syndrome until proven otherwise?

artículo científico publicado en 2015

Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada syndrome cohort

scientific article published on 02 March 2007

Exercise extreme caution when calling rare genetic variants novel arrhythmia syndrome susceptibility mutations ⬇️

artículo científico publicado el 13 de octubre de 2010

Exercise related syncope, when it's not the heart

artículo científico publicado en 2004

Exercise-induced ECG changes in Brugada syndrome.

artículo científico publicado en 2009

Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic features

artículo científico publicado en 2007

Facilitatory and inhibitory effects of SCN5A mutations on atrial fibrillation in Brugada syndrome ⬇️

artículo científico publicado el 26 de enero de 2011

Familial disease with a risk of sudden death: a longitudinal study of the psychological consequences of predictive testing for long QT syndrome

artículo científico publicado en 2008

Familial evaluation in catecholaminergic polymorphic ventricular tachycardia: disease penetrance and expression in cardiac ryanodine receptor mutation-carrying relatives

artículo científico publicado en 2012

Familial primary arrhythmia syndromes: Nice to know or need to know

artículo científico publicado en 2002

Familial sudden death is an important risk factor for primary ventricular fibrillation: a case-control study in acute myocardial infarction patients

artículo científico publicado en 2006

Fever increases the risk for cardiac arrest in the Brugada syndrome

scientific article published on 01 August 2008

Fever-Related Arrhythmic Events in the Multicenter Survey on Arrhythmic Events in Brugada Syndrome (SABRUS).

artículo científico publicado en 2018

Fever-induced QTc prolongation and ventricular arrhythmias in individuals with type 2 congenital long QT syndrome

artículo científico publicado en 2008

Fever-triggered ventricular arrhythmias in Brugada syndrome and type 2 long-QT syndrome.

artículo científico publicado en 2010

Fibrosis, Connexin-43, and Conduction Abnormalities in the Brugada Syndrome.

artículo científico publicado en 2015

First experience with the wearable cardioverter defibrillator in the Netherlands

artículo científico publicado en 2012

Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans

artículo científico publicado en 2009

Flecainide therapy reduces exercise-induced ventricular arrhythmias in patients with catecholaminergic polymorphic ventricular tachycardia

artículo científico publicado en 2011

Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands

artículo científico publicado en 2010

Founder mutations in the Netherlands: SCN5a 1795insD, the first described arrhythmia overlap syndrome and one of the largest and best characterised families worldwide

artículo científico publicado en 2009

Founder mutations in the Netherlands: familial idiopathic ventricular fibrillation and DPP6

artículo científico publicado en 2011

From whole exome sequencing to patient-specific therapy: another example of how basic research pays off in patient care

artículo científico publicado en 2015

Functional assessment of potential splice site variants in arrhythmogenic right ventricular dysplasia/cardiomyopathy

artículo científico publicado en 2014

GENCOR: a national registry for patients and families suffering from a familial heart disease in the Netherlands

artículo científico publicado en 2006

GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability

artículo científico publicado en 2016

GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability.

artículo científico publicado en 2016

Gain-of-function mutation in SCN5A causes ventricular arrhythmias and early onset atrial fibrillation

artículo científico publicado en 2017

Gender differences in patients with Brugada syndrome and arrhythmic events: Data from a survey on arrhythmic events in 678 patients

artículo científico publicado en 2018

Gender differences in the long QT syndrome: effects of beta-adrenoceptor blockade

artículo científico publicado en 2002

Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers.

artículo científico publicado en 2012

Gene-specific increase in the energetic cost of contraction in hypertrophic cardiomyopathy caused by thick filament mutations

article

Genetic Basis of Ventricular Arrhythmias.

artículo científico publicado en 2010

Genetic Causes in Cardiac Arrest Survivors: Fake News or the Real Deal?

scientific article published on 01 June 2017

Genetic Control of Potassium Channels

artículo científico publicado en 2016

Genetic Susceptibility for COVID-19-Associated Sudden Cardiac Death in African Americans

scientific article published on 04 May 2020

Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience

article

Genetic and clinical advances in congenital long QT syndrome

artículo científico publicado en 2014

Genetic arrhythmias complicating patients with dilated cardiomyopathy

artículo científico publicado en 2019

Genetic aspects of vasovagal syncope: a systematic review of current evidence

artículo científico publicado en 2009

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

artículo científico publicado en 2014

Genetic basis of malignant channelopathies and ventricular fibrillation in the structurally normal heart

scientific article published on May 2010

Genetic control of sodium channel function

artículo científico publicado en 2003

Genetic counseling and cardiac care in predictively tested hypertrophic cardiomyopathy mutation carriers: the patients' perspective.

artículo científico publicado en 2009

Genetic knowledge and counselling skills of Dutch cardiologists: sufficient for the genomics era?

artículo científico publicado en 2003

Genetic predisposition for sudden cardiac death in myocardial ischaemia: the Arrhythmia Genetics in the NEtherlandS study

artículo científico publicado en 2011

Genetic screening in acquired long QT syndrome? CAUTION: proceed carefully

artículo científico publicado en 2015

Genetic testing for inherited cardiac disease

artículo científico

Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants.

artículo científico publicado en 2009

Genetic testing in cardiovascular diseases

artículo científico publicado en 2010

Genetic variation in SCN10A influences cardiac conduction

artículo científico publicado en 2010

Genetically determined differences in sodium current characteristics modulate conduction disease severity in mice with cardiac sodium channelopathy

artículo científico publicado en 2009

Genetics of cardiac arrhythmias

artículo científico publicado en 2005

Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes

artículo científico publicado en 2013

Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction

artículo científico publicado en 2010

Genotype and clinical characteristics of congenital long QT syndrome in Thailand

artículo científico publicado en 2018

Genotype-phenotype aspects of type 2 long QT syndrome

artículo científico publicado en 2009

Genotype-phenotype dilemma in a case of sudden cardiac death with the E1053K mutation and a deletion in the SCN5A gene

artículo científico publicado en 2017

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

artículo científico publicado en 2002

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

scientific article published on 06 November 2006

HERG mutation predicts short QT based on channel kinetics but causes long QT by heterotetrameric trafficking deficiency.

artículo científico publicado en 2005

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).

artículo científico

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).

artículo científico publicado en 2011

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

scientific article published on 12 March 2009

Health-related quality of life impact of a transcatheter pacing system

scientific article published on 15 October 2018

Heart Rate Recovery After Exercise Is Associated With Arrhythmic Events in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

artículo científico publicado en 2020

Heart failure following STEMI: a contemporary cohort study of incidence and prognostic factors

artículo científico publicado en 2017

Heritability in genetic heart disease: the role of genetic background

scientific article published on 28 May 2019

High diagnostic yield and accuracy of history, physical examination, and ECG in patients with transient loss of consciousness in FAST: the Fainting Assessment study

artículo científico publicado en 2007

High distress in parents whose children undergo predictive testing for long QT syndrome

artículo científico publicado en 2005

High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics

article

How do hypertrophic cardiomyopathy mutations affect myocardial function in carriers with normal wall thickness? Assessment with cardiovascular magnetic resonance.

artículo científico publicado en 2010

I don't know what it is, but it doesn't feel right

artículo científico publicado en 2003

I think a niece of mine was referred to a neurologist

artículo científico publicado en 2004

IK1 modulates the U-wave: insights in a 100-year-old enigma.

artículo científico publicado en 2008

IKs in heart and hearing, the ear can do with less than the heart

artículo científico publicado en 2013

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

artículo científico publicado en 2008

Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals

artículo científico publicado en 2011

Identification of sarcomeric variants in probands with a clinical diagnosis of arrhythmogenic right ventricular cardiomyopathy (ARVC)

scientific article published on 21 May 2018

Images in cardiovascular medicine. Prominent crypt formation in the inferoseptum of a hypertrophic cardiomyopathy mutation carrier mimics noncompaction cardiomyopathy

scientific article published on 01 June 2007

Impact of Leadless Pacemaker Therapy on Cardiac and Atrioventricular Valve Function Through 12 Months of Follow-Up

scientific article published on 01 May 2019

Impact of cardiac complications on outcome after aneurysmal subarachnoid hemorrhage: a meta-analysis

artículo científico publicado en 2009

Impact of genetics on the clinical management of channelopathies

artículo científico publicado en 2013

Implantable cardioverter defibrillator as a bridge to recovery in an infant with cardiac rhabdomyoma

artículo científico publicado en 2008

Implantable cardioverter defibrillator therapy in adults with congenital heart disease: who is at risk of shocks?

artículo científico publicado en 2011

Implantable cardioverter-defibrillator harm in young patients with inherited arrhythmia syndromes: A systematic review and meta-analysis of inappropriate shocks and complications

artículo científico publicado en 2015

Importance of Validating Guideline Recommendations

artículo científico publicado en 2020

Improving long QT syndrome diagnosis by a polynomial-based T-wave morphology characterization

artículo científico publicado en 2020

Improving the care for female subcutaneous ICD patients: A qualitative study of gender-specific issues

artículo científico publicado en 2020

Improving usual care after sudden death in the young with focus on inherited cardiac diseases (the CAREFUL study): a community-based intervention study.

artículo científico publicado en 2015

In Children and Adolescents From Brugada Syndrome-Families, Only SCN5A Mutation Carriers Develop a Type-1 ECG Pattern Induced By Fever

artículo científico publicado en 2020

In search of the holy grail in the channelopathy field: Proving pathogenicity of long QT syndrome-associated variants?

artículo científico publicado en 2017

In silico cardiac risk assessment in patients with long QT syndrome: type 1: clinical predictability of cardiac models

artículo científico publicado en 2012

In-hospital cardiac arrest is associated with use of non-antiarrhythmic QTc-prolonging drugs

artículo científico publicado en 2006

Inaccessibility to quinidine therapy is about to get worse

artículo científico publicado en 2013

Inappropriate shocks in the subcutaneous ICD: Incidence, predictors and management.

artículo científico publicado en 2015

Inappropriate subcutaneous implantable cardioverter-defibrillator shocks due to T-wave oversensing can be prevented: implications for management

artículo científico publicado en 2013

Incidence, causes, and outcomes of out-of-hospital cardiac arrest in children. A comprehensive, prospective, population-based study in the Netherlands

artículo científico publicado en 2011

Induced pluripotent stem cell derived cardiomyocytes as models for cardiac arrhythmias

artículo científico publicado en 2012

Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies

artículo científico publicado en 2012

Is there a genetic basis for malignant ventricular arrhythmias?

artículo científico publicado en 2005

It's not what you think it is.

artículo científico publicado en 2005

J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge

artículo científico publicado en 2016

J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge

scientific article published on 01 April 2017

J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge.

artículo científico publicado en 2016

Just one collapse during soccer

artículo científico publicado en 2004

Lack of genotype-phenotype correlation in Brugada Syndrome and Sudden Arrhythmic Death Syndrome families with reported pathogenic SCN1B variants

scientific article published on 11 May 2018

Lamin A/C mutation is independently associated with an increased risk of arterial and venous thromboembolic complications

artículo científico publicado en 2012

Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci

artículo científico publicado en 2012

Late sodium current inhibition in acquired and inherited ventricular (dys)function and arrhythmias

artículo científico publicado en 2013

Leadless pacemaker implantation after explantation of infected conventional pacemaker systems: A viable solution?

scientific article published on 06 July 2018

Left Axis Deviation in Brugada Syndrome: Vectorcardiographic Evaluation during Ajmaline Provocation Testing Reveals Additional Depolarization Abnormalities

artículo científico publicado en 2021

Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardia

artículo científico publicado en 2008

Left cardiac sympathetic denervation in the Netherlands for the treatment of inherited arrhythmia syndromes

scientific article published on April 2014

Letter by Amin et al Regarding Article, "Genetic Modifiers for the Long-QT Syndrome: How Important Is the Role of Variants in the 3' Untranslated Region of KCNQ1?"

artículo científico publicado en 2016

Life-threatening arrhythmias with autosomal recessive TECRL variants

artículo científico publicado en 2020

Linking the heart and the brain: Neurodevelopmental disorders in patients with catecholaminergic polymorphic ventricular tachycardia

artículo científico publicado en 2018

Local depolarization abnormalities are the dominant pathophysiologic mechanism for type 1 electrocardiogram in brugada syndrome a study of electrocardiograms, vectorcardiograms, and body surface potential maps during ajmaline provocation

artículo científico publicado en 2010

Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies.

artículo científico publicado en 2006

Long QT syndrome: a double hit hurts more

artículo científico publicado en 2010

Long QT syndrome: beyond the causal mutation

artículo científico

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

artículo científico publicado en 2005

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

artículo científico publicado en 2010

Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?

artículo científico

Loss-of-function sodium channel mutations in infancy: a pattern unfolds

scientific article published on 16 November 2011

Low rate of cardiac events in first-degree relatives of diagnosis-negative young sudden unexplained death syndrome victims during follow-up

scientific article published on 29 May 2014

Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: determining the best cardiological screening strategy

artículo científico publicado en 2011

Mechanism of right precordial ST-segment elevation in structural heart disease: excitation failure by current-to-load mismatch.

artículo científico publicado en 2009

Mechanisms of inherited cardiac conduction disease

artículo científico publicado en 2005

Microvolt T-wave alternans during exercise and pacing are not comparable

artículo científico publicado en 2009

Midterm Safety and Performance of a Leadless Cardiac Pacemaker: 3-Year Follow-up to the LEADLESS Trial (Nanostim Safety and Performance Trial for a Leadless Cardiac Pacemaker System).

artículo científico publicado en 2018

Mild-to-moderate kidney dysfunction and the risk of sudden cardiac death in the setting of acute myocardial infarction

artículo científico publicado en 2011

Minimal defibrillation thresholds and the correlation with implant position in subcutaneous implantable-defibrillator patients

artículo científico publicado en 2019

Mortality Risk Associated With Truncating Founder Mutations in Titin

artículo científico publicado en 2019

Mortality of Inherited Arrhythmia Syndromes

artículo científico publicado en 2012

Mortality risk of untreated myosin-binding protein C-related hypertrophic cardiomyopathy: insight into the natural history

artículo científico publicado en 2011

Mothers with long QT syndrome are at increased risk for fetal death: findings from a multicenter international study

scientific article published on 11 September 2019

Multifocal ectopic Purkinje-related premature contractions: a new SCN5A-related cardiac channelopathy

artículo científico publicado en 2012

Multilevel analyses of SCN5A mutations in arrhythmogenic right ventricular dysplasia/cardiomyopathy suggest non-canonical mechanisms for disease pathogenesis

artículo científico publicado en 2017

Mutation and gender-specific risk in type 2 long QT syndrome: implications for risk stratification for life-threatening cardiac events in patients with long QT syndrome

artículo científico publicado en 2011

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

artículo científico publicado en 2004

Mutation location effect on severity of phenotype during exercise testing in type 1 long-QT syndrome: impact of transmembrane and C-loop location

artículo científico publicado en 2013

Mutations in conserved amino acids in the KCNQ1 channel and risk of cardiac events in type-1 long-QT syndrome

artículo científico publicado en 2009

Myocardial fibrosis as an early feature in phospholamban p.Arg14del mutation carriers: phenotypic insights from cardiovascular magnetic resonance imaging

artículo científico publicado en 2019

Myocarditis in patients with subarachnoid hemorrhage: A histopathologic study

artículo científico publicado en 2015

Myocyte necrosis underlies progressive myocardial dystrophy in mouse dsg2-related arrhythmogenic right ventricular cardiomyopathy

scientific article published on 27 July 2009

Na+ channel mutation leading to loss of function and non-progressive cardiac conduction defects

artículo científico publicado en 2003

Narrow QRS complexes intervening wide QRS complexes

Narrow QRS complexes intervening wide QRS complexes.

artículo científico publicado en 2012

Navigating the mini-maze: systematic review of the first results and progress of minimally-invasive surgery in the treatment of atrial fibrillation

artículo científico publicado en 2013

New ECG criteria in arrhythmogenic right ventricular dysplasia/cardiomyopathy

scientific article published on 07 July 2009

Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy

scientific article published on 23 July 2019

Nightly phenomena, day time work?

artículo científico publicado en 2004

Nodoventricular accessory pathways in PRKAG2-dependent familial preexcitation syndrome reveal a disorder in cardiac development.

artículo científico publicado en 2008

Non-compaction: a distinct cardiomyopathy or non-specific morphological trait?

artículo científico publicado en 2008

Not all beta-blockers are equal in the management of long QT syndrome types 1 and 2: higher recurrence of events under metoprolol

artículo científico publicado en 2012

Not just any ICD device in patients with long-QT syndrome

artículo científico publicado en 2007

Novel electrocardiographic criteria for the diagnosis of arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2015

Now you see it, now you don't

artículo científico publicado en 2005

Obtaining insurance after DNA diagnostics: a survey among hypertrophic cardiomyopathy mutation carriers

artículo científico publicado en 2009

One to one, one to two, two to one? What is the rhythm?

artículo científico publicado en 2004

Out of the frying pan and into the fire

artículo científico publicado en 2004

Outcome in phospholamban R14del carriers: results of a large multicentre cohort study

artículo científico publicado en 2014

Outpatient treatment with the wearable cardioverter defibrillator: clinical experience in two Dutch centres

artículo científico publicado en 2017

Overlap syndrome of cardiac sodium channel disease in mice carrying the equivalent mutation of human SCN5A-1795insD

artículo científico publicado en 2006

P336Exome sequencing of multiple affected individuals from an Irish family with Brugada Syndrome uncovers a novel locus for the disorder

Palpitations again, have a close look

artículo científico publicado en 2006

Palpitations and dizziness in a 65-year-old man.

artículo científico publicado en 2006

Palpitations in a 19-year old man and a slow heart rate at rest

artículo científico publicado en 2013

Palpitations in a 19-year old man and a slow heart rate at rest

article published in 2013

Palpitations in a 19-year-old man, take a second look

artículo científico publicado en 2013

Palpitations in a 19-year-old man, take a second look

artículo científico publicado en 2013

Palpitations, once again

Palpitations, once again

Palpitations, should one worry?

artículo científico publicado en 2013

Palpitations, should one worry?

artículo científico publicado en 2013

Pathophysiological mechanisms of Brugada syndrome: depolarization disorder, repolarization disorder, or more?

artículo científico publicado en 2005

Penetrance of Hypertrophic Cardiomyopathy in Children Who Are Mutation Positive

artículo científico publicado en 2017

Permanent leadless cardiac pacing: results of the LEADLESS trial.

artículo científico

Phenotypical manifestations of mutations in the genes encoding subunits of the cardiac sodium channel

scientific article published on April 2011

Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogenic cardiomyopathy

artículo científico publicado en 2012

Phylogenetic and physicochemical analyses enhance the classification of rare nonsynonymous single nucleotide variants in type 1 and 2 long-QT syndrome

artículo científico publicado en 2012

Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy

artículo científico publicado en 2006

Postmortem Histopathological Examination of a Leadless Pacemaker Shows Partial Encapsulation After 19 Months

artículo científico publicado en 2015

Postpacing abnormal repolarization in catecholaminergic polymorphic ventricular tachycardia associated with a mutation in the cardiac ryanodine receptor gene.

artículo científico publicado en 2011

Prediction of ventricular arrhythmia in phospholamban p.Arg14del mutation carriers-reaching the frontiers of individual risk prediction

artículo científico publicado en 2021

Pregnancy and the risk of torsades de pointes in congenital long-QT syndrome

artículo científico publicado en 2008

Prevalence and characterization of ECG abnormalities after intracerebral hemorrhage

artículo científico publicado en 2010

Primary prevention: prime time?: ICD trials (and tribulations).

artículo científico publicado en 2004

Primary ventricular fibrillation in acute myocardial infarction: an inherited disease?

artículo científico publicado en 2001

Profile of Brugada Syndrome Patients Presenting with Their First Documented Arrhythmic Event. Data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS).

artículo científico publicado en 2018

Prognosis among survivors of primary ventricular fibrillation in the percutaneous coronary intervention era

article

Prognostic implications of mutation-specific QTc standard deviation in congenital long QT syndrome

artículo científico publicado en 2013

Prognostic significance of fever-induced Brugada syndrome.

artículo científico publicado en 2016

Programmed Ventricular Stimulation for Risk Stratification in the Brugada Syndrome: A Pooled Analysis

artículo científico publicado en 2016

Prophylactic (hydroxy)chloroquine in COVID-19: potential relevance for cardiac arrhythmia risk

artículo científico publicado en 2020

Proposed Diagnostic Criteria for the Brugada Syndrome

article published in 2002

Proposed diagnostic criteria for the Brugada syndrome

artículo científico publicado en 2002

Proposed diagnostic criteria for the Brugada syndrome: consensus report

artículo científico publicado en 2002

QT prolongation and mortality in hospital settings: identifying patients at high risk

scientific article published on 01 April 2013

Quality of life and psychological distress in hypertrophic cardiomyopathy mutation carriers: a cross-sectional cohort study.

artículo científico publicado en 2009

Quantitative trait loci for electrocardiographic parameters and arrhythmia in the mouse

scientific article published on 18 September 2010

Quinidine, a life-saving medication for Brugada syndrome, is inaccessible in many countries

artículo científico publicado en 2013

Rationale and design of the CAREFUL study : The yield of CARdiogenetic scrEening in First degree relatives of sudden cardiac and UnexpLained death victims <45 years

artículo científico publicado en 2010

Rationale and design of the PRAETORIAN trial: a Prospective, RAndomizEd comparison of subcuTaneOus and tRansvenous ImplANtable cardioverter-defibrillator therapy

scientific article published on 01 May 2012

Rationale and design of the PRAETORIAN-DFT trial: A prospective randomized CompArative trial of SubcutanEous ImplanTable CardiOverter-DefibrillatoR ImplANtation with and without DeFibrillation testing

scientific article published on 16 May 2019

Rationale of the SEAS study: Serial Echocardiography After Subarachnoid haemorrhage, a prospective national, multicentre, multidisciplinary, cohort study to evaluate cardiac abnormalities following intracranial haemorrhage

artículo científico publicado en 2006

Readthrough-Promoting Drugs Gentamicin and PTC124 Fail to Rescue Nav1.5 Function of Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes Carrying Nonsense Mutations in the Sodium Channel Gene SCN5A.

artículo científico publicado en 2016

Reappraisal of Reported Genes for Sudden Arrhythmic Death: An Evidence-Based Evaluation of Gene Validity for Brugada Syndrome

article

Rebuttal to EP testing predicts cardiac events in patients with Brugada syndrome

artículo científico publicado en 2011

Recent breakthroughs in the genetics of atrial fibrillation

artículo científico publicado en 2003

Recurrent and Founder Mutations in the Netherlands: the Long-QT Syndrome

artículo científico publicado en 2010

Recurrent and founder mutations in the Netherlands : Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasia

artículo científico publicado en 2010

Recurrent and founder mutations in the Netherlands-Phospholamban p.Arg14del mutation causes arrhythmogenic cardiomyopathy

artículo científico publicado en 2013

Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation

artículo científico publicado en 2008

Relation Between Basic and Clinical Electrophysiologic Characteristics in Brugada Syndrome: Facts or Fiction? ⬇️

artículo científico publicado el 1 de abril de 2003

Relationship Between Cardiac Dysfunction and Cerebral Perfusion in Patients with Aneurysmal Subarachnoid Hemorrhage.

artículo científico publicado en 2016

Reply: Search for Evidence-Based Medicine for Brugada Syndrome: The Complex Network of the Brugada Syndrome.

artículo científico publicado en 2016

Repolarization Versus Depolarization Defects in Brugada Syndrome: A Tale of 2 Different Electrophysiologic Settings?

artículo científico publicado en 2017

Response by Wilde and Gollob to Letter Regarding Article, "Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada Syndrome"

scientific article published on 01 April 2019

Response to Letters Regarding Article, "Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia: The Role of Left Cardiac Sympathetic Denervation".

artículo científico publicado en 2016

Response to letter from Drs. Li et al. regarding our paper in Int. J. Cardiol. 2018. Doi: 10.1016/j.ijcard.2017.09.010: SCN5A mutation type and topology are associated with the risk of ventricular arrhythmia by sodium channel blockers

scientific article published on 01 November 2018

Revisiting the sensitivity of sodium channel blocker testing in Brugada syndrome using obligate transmittance

artículo científico publicado en 2017

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

artículo científico publicado en 2005

Right you are.

artículo científico publicado en 2005

Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers

scientific article published on 01 January 2012

Risk Stratification in Brugada Syndrome: The "Impossible" Made Possible?

artículo científico publicado en 2016

Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT syndrome and normal-range corrected QT intervals

artículo científico publicado en 2011

Risk stratification for sudden cardiac death in hypertrophic cardiomyopathy: Dutch cardiologists and the care of mutation carriers

artículo científico publicado en 2009

Risk stratification for sudden cardiac death in hypertrophic cardiomyopathy: systematic review of clinical risk markers

artículo científico publicado en 2010

Risk stratification in Brugada syndrome: Where is the finish line?

scientific article published on 03 August 2016

Role of Genetic Testing in Patients with Ventricular Arrhythmias in Apparently Normal Hearts

artículo científico publicado en 2016

Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study.

artículo científico publicado en 2015

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

artículo científico publicado en 2007

Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndrome

artículo científico publicado en 2005

Role of the Purkinje system in heritable arrhythmias

artículo científico publicado en 2019

SARS-CoV-2, COVID-19 and inherited arrhythmia syndromes

scientific article published on 31 March 2020

SCN5A Mutation Type and a Genetic Risk Score Associate Variably with Brugada Syndrome Phenotype in SCN5A Families

artículo científico publicado en 2020

SCN5A mutation type and topology are associated with the risk of ventricular arrhythmia by sodium channel blockers

artículo científico publicado en 2018

SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome

artículo científico publicado en 2009

SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups

artículo científico publicado en 2018

SCN5A mutations in Brugada syndrome are associated with increased cardiac dimensions and reduced contractility

artículo científico publicado en 2012

SCN5A overlap syndromes: no end to disease complexity?

artículo científico publicado en 2008

SCN5A variants in Brugada syndrome: True, true false or false true

scientific article published on 12 November 2018

SNPs identified as modulators of ECG traits in the general population do not markedly affect ECG traits during acute myocardial infarction nor ventricular fibrillation risk in this condition.

artículo científico publicado en 2013

ST-Segment Elevation and Fractionated Electrograms in Brugada Syndrome Patients Arise From the Same Structurally Abnormal Subepicardial RVOT Area but Have a Different Mechanism

artículo científico publicado en 2015

Safe drug use in long QT syndrome and Brugada syndrome: comparison of website statistics

artículo científico publicado en 2013

Scar tissue and microvolt T-wave alternans

artículo científico publicado en 2014

Should I be worried?

artículo científico publicado en 2006

Slow and Discontinuous Conduction Conspire in Brugada Syndrome: A Right Ventricular Mapping and Stimulation Study

artículo científico publicado en 2008

Sodium Channelopathies: Do We Really Understand What's Going On? ⬇️

artículo científico publicado el 31 de agosto de 2010

Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans

artículo científico publicado en 2008

Somatic mosaicism contributes to phenotypic variation in Timothy syndrome

scientific article published on 09 September 2011

Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test

artículo científico publicado en 2009

Spontaneous electrocardiographic fluctuations in Brugada syndrome: does it matter?

artículo científico publicado en 2006

Structural abnormalities of the inferoseptal left ventricular wall detected by cardiac magnetic resonance imaging in carriers of hypertrophic cardiomyopathy mutations

artículo científico publicado en 2006

Structurally Abnormal Myocardium Underlies Ventricular Fibrillation Storms in a Patient Diagnosed With the Early Repolarization Pattern

artículo científico publicado en 2020

Subcutaneous or Transvenous Defibrillator Therapy

artículo científico publicado en 2020

Subsequent Event Risk in Individuals With Established Coronary Heart Disease

artículo científico publicado en 2019

Substitution of a conserved alanine in the domain IIIS4-S5 linker of the cardiac sodium channel causes long QT syndrome

artículo científico publicado en 2005

Sudden Cardiac Arrest and Rare Genetic Variants in the Community.

artículo científico publicado en 2016

Sudden Cardiac Death Prediction in Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC): A Multinational Collaboration

scientific article published on 09 December 2020

Sudden cardiac death in the young: the molecular autopsy and a practical approach to surviving relatives.

artículo científico

Sudden death in the young: what do we know about it and how to prevent?

artículo científico publicado en 2010

Sudden unexplained death: heritability and diagnostic yield of cardiological and genetic examination in surviving relatives.

artículo científico publicado en 2005

Support vector machine-based assessment of the T-wave morphology improves long QT syndrome diagnosis

artículo científico publicado en 2018

Supraventricular tachycardias, conduction disease, and cardiomyopathy in 3 families with the same rare variant in TNNI3K (p.Glu768Lys)

artículo científico publicado en 2018

Surgical Management of Implantation-Related Complications of the Subcutaneous Implantable Cardioverter-Defibrillator

artículo científico publicado en 2015

Switch From Fetal to Adult SCN5A Isoform in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction Disease-Causing Mutation

artículo científico publicado en 2017

Symptoms and signs of syncope: a review of the link between physiology and clinical clues

artículo científico publicado en 2009

Syncope and exercise-related ventricular tachycardia.

artículo científico publicado en 2012

Syncope during exercise, documented with continuous blood pressure monitoring during ergometer testing

artículo científico publicado en 2005

Syncope in Brugada syndrome: prevalence, clinical significance, and clues from history taking to distinguish arrhythmic from nonarrhythmic causes

artículo científico publicado en 2014

Syncope in genotype-negative long QT syndrome family members

artículo científico publicado en 2014

T-cell-mediated inflammatory activity in the stellate ganglia of patients with ion-channel disease and severe ventricular arrhythmias.

artículo científico publicado en 2014

T-wave alternans in a patient with long-QT syndrome type 3.

artículo científico publicado en 2006

TDI-echocardiography: a new screening tool for long QT syndrome?

artículo científico publicado en 2003

TGFβ-inducible early gene-1 (TIEG1) mutations in hypertrophic cardiomyopathy

artículo científico publicado en 2012

Targeting sodium channels in cardiac arrhythmia

artículo científico publicado en 2013

Ten years of genes in inherited arrhythmia syndromes: an example of what we have learned from patients, electrocardiograms, and computers

artículo científico publicado en 2005

The "accordion sign," a new tune in arrhythmogenic right ventricular dysplasia/cardiomyopathy magnetic resonance imaging?

artículo científico publicado en 2009

The 'president's drug'

artículo científico publicado en 2020

The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands

scientific article published on 01 October 2003

The AV-node revisited.

artículo científico publicado en 2003

The Brugada ECG pattern: a marker of channelopathy, structural heart disease, or neither? Toward a unifying mechanism of the Brugada syndrome.

artículo científico publicado en 2010

The Brugada Syndrome Susceptibility Gene HEY2 Modulates Cardiac Transmural Ion Channel Patterning and Electrical Heterogeneity.

artículo científico publicado en 2017

The ECG of a (cardio)myopathy?

artículo científico publicado en 2005

The ICD for primary prevention in patients with inherited cardiac diseases: indications, use, and outcome: a comparison with secondary prevention

artículo científico publicado en 2012

The Netherlands Arrhythmogenic Cardiomyopathy Registry: design and status update

scientific article published on 01 October 2019

The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading [...]

artículo científico publicado en 2009

The Shanghai Score System in Brugada Syndrome: Using it Beyond a Diagnostic Score

scientific article published on 01 June 2018

The brisk-standing-test for long QT syndrome in prepubertal school children: defining normal.

artículo científico publicado en 2017

The cardiac sodium channel displays differential distribution in the conduction system and transmural heterogeneity in the murine ventricular myocardium

artículo científico publicado en 2009

The cardiac sodium channel gene SCN5A and its gene product NaV1.5: Role in physiology and pathophysiology.

artículo científico

The chemical compound PTC124 does not affect cellular electrophysiology of cardiac ventricular myocytes.

artículo científico publicado en 2012

The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification.

artículo científico publicado en 2007

The complexity of genotype-phenotype relations associated with loss-of-function sodium channel mutations and the role of in silico studies.

artículo científico publicado en 2008

The development and validation of an easy to use automatic QT-interval algorithm.

artículo científico publicado en 2017

The diagnostic and therapeutic aspects of loss-of-function cardiac sodium channelopathies in children

artículo científico publicado en 2012

The effect of revascularization of a chronic total coronary occlusion on electrocardiographic variables. A sub-study of the EXPLORE trial

artículo científico publicado en 2018

The entirely subcutaneous implantable cardioverter-defibrillator: initial clinical experience in a large Dutch cohort

artículo científico publicado en 2012

The genetic architecture of long QT syndrome: A critical reappraisal.

artículo científico publicado en 2018

The ions have it.

artículo científico publicado en 2005

The measurement of the QT interval

artículo científico publicado en 2014

The molecular genetics of arrhythmias

artículo científico publicado en 2005

The multifaceted cardiac sodium channel and its clinical implications

artículo científico

The need to continue screening for hypertrophic cardiomyopathy after adolescence

artículo científico publicado en 2015

The never ending story of risk stratification for sudden death in hypertrophic cardiomyopathy

artículo científico publicado en 2011

The pathophysiological mechanism underlying Brugada syndrome: depolarization versus repolarization

artículo científico publicado en 2010

The patient with hypertrophic cardiomyopathy has a family ⬇️

artículo científico publicado el 1 de febrero de 2011

The phenomenon of "QT stunning": the abnormal QT prolongation provoked by standing persists even as the heart rate returns to normal in patients with long QT syndrome

artículo científico publicado en 2012

The phenotype is equally important in promoting variants from benign to pathogenic as well as in demoting variants from pathogenic to benign

artículo científico publicado en 2018

The primary arrhythmia syndromes: same mutation, different manifestations. Are we starting to understand why?

artículo científico publicado en 2008

The relationship between pre-participation screening of young competitive athletes and family screening

artículo científico publicado en 2009

The response of the QT interval to the brief tachycardia provoked by standing: a bedside test for diagnosing long QT syndrome

artículo científico publicado en 2010

The role of renin-angiotensin-aldosterone system polymorphisms in phenotypic expression of MYBPC3-related hypertrophic cardiomyopathy

artículo científico publicado en 2012

The role of the epinephrine test in the diagnosis and management of children suspected of having congenital long QT syndrome

artículo científico publicado en 2009

The sense and nonsense of direct-to-consumer genetic testing for cardiovascular disease

artículo científico publicado en 2011

The site of origin of torsade de pointes

artículo científico publicado en 2011

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

artículo científico publicado en 2003

The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy

artículo científico publicado en 2019

The yield of risk stratification for sudden cardiac death in hypertrophic cardiomyopathy myosin-binding protein C gene mutation carriers: focus on predictive screening

scientific article published on 16 December 2009

The β-angle can help guide clinical decisions in the diagnostic work-up of patients suspected of Brugada syndrome: a validation study of the β-angle in determining the outcome of a sodium channel provocation test

artículo científico publicado en 2021

Therapeutic approach for patients with catecholaminergic polymorphic ventricular tachycardia: state of the art and future developments

artículo científico publicado en 2011

Therapeutic approaches for Long QT syndrome type 3: an update

artículo científico publicado en 2018

Think twice before you tell

artículo científico publicado en 2014

Think twice before you tell

artículo científico publicado en 2014

Thoracoscopic Video-Assisted Pulmonary Vein Antrum Isolation, Ganglionated Plexus Ablation, and Periprocedural Confirmation of Ablation Lesions: First Results of a Hybrid Surgical-Electrophysiological Approach for Atrial Fibrillation

artículo científico publicado en 2011

Time-to-first appropriate shock in patients implanted prophylactically with an implantable cardioverter-defibrillator: data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS)

scientific article published on 01 May 2019

To Add or Not to Add Mitral Valve Surgery to Septal Myectomy in HOCM Patients

artículo científico publicado en 2017

Transthyretin amyloidosis: a phenocopy of hypertrophic cardiomyopathy

scientific article published on 05 May 2017

Treatment for patients with catecholaminergic polymorphic ventricular tachycardia: are we in need of randomized trials?

artículo científico publicado en 2012

Treatment of Atrial and Ventricular Arrhythmias Through Autonomic Modulation

artículo científico publicado en 2015

Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathy

artículo científico publicado en 2016

Two siblings with early repolarization syndrome: clinical and genetic characterization by whole-exome sequencing

artículo científico publicado en 2020

Two-incision technique for implantation of the subcutaneous implantable cardioverter-defibrillator

artículo científico publicado en 2013

Type 8 long QT syndrome: pathogenic variants in CACNA1C-encoded Cav1.2 cluster in STAC protein binding site

scientific article published on 01 November 2019

Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathies

artículo científico publicado en 2008

Understanding torsade de pointes: a bridge to tailored drug therapy?

artículo científico publicado en 2002

Unidentified candidates for cardiac resynchronization therapy: guideline adherence in a large academic outpatient clinic in the Netherlands

artículo científico publicado en 2012

Unmasking of brugada syndrome by lithium

artículo científico publicado en 2005

Use of mutant-specific ion channel characteristics for risk stratification of long QT syndrome patients

artículo científico publicado en 2011

Using registries to predict outcome: the implantable cardioverter-defibrillator in long QT syndrome

artículo científico publicado en 2019

Value of history-taking in syncope patients: in whom to suspect long QT syndrome?

artículo científico publicado en 2009

Value of serial heart rate variability measurement for prediction of appropriate ICD discharge in patients with heart failure.

artículo científico publicado en 2013

Variable Na(v)1.5 protein expression from the wild-type allele correlates with the penetrance of cardiac conduction disease in the Scn5a(+/-) mouse model

artículo científico publicado en 2010

Variants in the 3' untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner

artículo científico publicado en 2011

Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes

artículo científico publicado en 2016

Vasovagal syncope or ventricular fibrillation. Your diagnosis better be accurate

artículo científico publicado en 2007

Ventricular dysfunction in a family with long QT syndrome type 3.

artículo científico publicado en 2013

Ventricular fibrillation in MYH7-related hypertrophic cardiomyopathy before onset of ventricular hypertrophy

artículo científico publicado en 2009

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

artículo científico publicado en 2009

Voltage-gated sodium channels: action players with many faces

artículo científico publicado en 2006

Where do the extras come from?

artículo científico publicado en 2005

Which patients are not suitable for a subcutaneous ICD: incidence and predictors of failed QRS-T-wave morphology screening

artículo científico publicado en 2014

Who are the long-QT syndrome patients who receive an implantable cardioverter-defibrillator and what happens to them?: data from the European Long-QT Syndrome Implantable Cardioverter-Defibrillator (LQTS ICD) Registry

artículo científico publicado en 2010

Why did this patient experience a sudden cardiac arrest? Follow your curiosity!

artículo científico publicado en 2019

Wide complexes intervening regular sinus rhythm

artículo científico publicado en 2006

Yield and Pitfalls of Ajmaline Testing in the Evaluation of Unexplained Cardiac Arrest and Sudden Unexplained Death: Single-Center Experience With 482 Families

scientific article published on 28 June 2017

Yield of molecular and clinical testing for arrhythmia syndromes: report of 15 years' experience.

artículo científico publicado en 2013

Yield of the RYR2 Genetic Test in Suspected Catecholaminergic Polymorphic Ventricular Tachycardia and Implications for Test Interpretation

artículo científico publicado en 2018

[Premature sudden death--consider serious familial heart rhythm disturbances]

artículo científico publicado en 2011

[The optimal treatment of chronic heart failure with beta-blockers may be dependent upon the genetic background of the patient]

scientific article published on 01 July 2007

[Thoracoscopic treatment of atrial fibrillation]

scientific article published on 01 January 2012

hiPSC-derived cardiomyocytes from Brugada Syndrome patients without identified mutations do not exhibit clear cellular electrophysiological abnormalities

scientific article published on 03 August 2016

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