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List of works by Ramon Brugada

'Localized' right ventricular morphological abnormalities in patients with the Brugada syndrome: what is their significance?

scientific article published on 01 June 2001

A Genetically Vulnerable Myocardium May Predispose to Myocarditis.

scientific article published in December 2015

A common mutation in methylenetetrahydrofolate reductase gene is not a major risk of coronary artery disease or myocardial infarction

scientific article published in January 1997

A missense mutation in the sodium channel β1b subunit reveals SCN1B as a susceptibility gene underlying long QT syndrome

scientific article published in July 2014

A missense mutation in the sodium channel β2 subunit reveals SCN2B as a new candidate gene for Brugada syndrome.

scientific article published on 29 April 2013

A mutation in the sodium channel is responsible for the association of long QT syndrome and familial atrial fibrillation

scientific article

A nonsense SCN5A mutation associated with Brugada-type electrocardiogram and intraventricular conduction defects

scientific article published on September 2009

A novel missense mutation, I890T, in the pore region of cardiac sodium channel causes Brugada syndrome

scientific article

A novel mutation in lamin a/c causing familial dilated cardiomyopathy associated with sudden cardiac death

scientific article published on 9 December 2014

A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia.

scientific article published on 9 December 2016

A prospective study of paraoxonase gene Q/R192 polymorphism and severity, progression and regression of coronary atherosclerosis, plasma lipid levels, clinical events and response to fluvastatin

scientific article published in February 2001

A reply

scientific article published on 01 September 2000

A transgenic rabbit model for human hypertrophic cardiomyopathy

scientific article

ABSTRACTS

scholarly article

Acute, Exercise Dose-Dependent Impairment in Atrial Performance During an Endurance Race: 2D Ultrasound Speckle-Tracking Strain Analysis

scientific article published on 11 August 2016

Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy.

scientific article published on 3 August 2017

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

scientific article published on 18 December 2017

Age, Genetics, and Fibrosis in the Brugada Syndrome

scientific article published on 01 November 2015

An SCN1B Variant Affects Both Cardiac-Type (NaV1.5) and Brain-Type (NaV1.1) Sodium Currents and Contributes to Complex Concomitant Brain and Cardiac Disorders

scientific article published on 29 September 2020

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

scientific article

Analysis of Brugada syndrome loci reveals that fine-mapping clustered GWAS hits enhances the annotation of disease-relevant variants

scientific article published on 20 April 2021

Analysis of mRNA from human heart tissue and putative applications in forensic molecular pathology.

scientific article

Analysis of the arrhythmogenic substrate in human heart failure

scientific article published in October 2012

Arrhythmia and Right Heart Disease: From Genetic Basis to Clinical Practice ⬇️

scientific article published on August 1, 2010

Arrhythmia induction by antiarrhythmic drugs

scientific article published on 01 March 2000

Arrhythmogenic right ventricular cardiomyopathy: severe structural alterations are associated with inflammation

scientific article published on 03 September 2012

Asymptomatic patients with a brugada electrocardiogram: are they at risk?

scientific article published on 01 January 2001

Atrial fibrillation: evidence for genetically determined disease

scientific article published on May 2008

Atrial fibrillation: is the solution in the genes? ⬇️

scientific article published on 01 June 1997

Autopsy investigation and Bayesian approach to coronary artery disease in victims of motor-vehicle accidents.

scientific article published on 20 May 2011

Brugada Syndrome

scientific article (by Brugada)

Brugada Syndrome and Exercise Practice: Current Knowledge, Shortcomings and Open Questions

scientific article published on 01 July 2017

Brugada Syndrome and Exercise Practice: Current Knowledge, Shortcomings and Open Questions.

scientific article

Brugada Syndrome and PKP2: Evidences and uncertainties

scientific article published on 07 April 2016

Brugada Syndrome: Overview

Brugada syndrome

scientific article published in July 1999

Brugada syndrome

scientific article published on 01 July 2008

Brugada syndrome

scientific article published on 01 July 2011

Brugada syndrome

scientific article published on 01 January 2014

Brugada syndrome and p.E61X_RANGRF.

scientific article

Brugada syndrome unmasked by pneumonia

scientific article published on January 2006

Brugada syndrome with marked conduction disease: dual implications of a SCN5A mutation

scientific article published in May 2008

Brugada syndrome: 12 years of progression

scientific article

Brugada syndrome: 1992-2002: a historical perspective

scientific article published in May 2003

Brugada syndrome: a decade of progress

scientific article published in December 2002

Brugada syndrome: clinical and genetic findings.

scientific article published on 23 April 2015

Brugada syndrome: diagnostic pitfalls

scientific article published on 25 March 2009

Brugada syndrome: from cell to bedside

scientific article

Brugada syndrome: report of the second consensus conference.

scientific article

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

scientific article

Brugada syndrome: the syndrome of right bundle branch block, ST segment elevation in V1 to V3 and sudden death.

scientific article published on October 2001

Brugada syndrome: update 2009

scientific article published on 01 September 2009

Brugada syndrome: why are there multiple answers to a simple question?

scientific article published on 01 December 2001

Cardiac Channelopathies and Sudden Death: Recent Clinical and Genetic Advances

scientific article published on 29 January 2017

Cardiac arrest and left ventricular fibrosis in a Finnish family with the lamin A/C mutation

scientific article published on 21 November 2007

Cardiovascular translational medicine (IV): The genetic basis of malignant arrhythmias and cardiomyopathies.

scientific article published on April 2009

Changes in plasma cholesterol levels after hospitalization for acute coronary events

scientific article published on 01 May 1996

Channelopathies: a new category of diseases causing sudden death

scientific article published on May 2007

Characteristics of inverse-computed epicardial electrograms of Brugada syndrome patients

scientific article published on 01 January 2011

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

scientific article published on 01 April 2019

Characterization of Electrocardiographic Findings in Young Students

scientific article published on 01 October 2018

Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis

scientific article published on 01 July 2020

Clinical Prognosis of Right-Sided Infective Endocarditis not Associated with Cardiac Devices or Intravenous Drug use: a Cohort Study and Meta-Analysis

scientific article published on 28 April 2020

Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardia

scientific article published in July 2015

Clinical approaches to tachyarrhythmias, volume 10: The brugada syndrome

Clinical heterogeneity in sodium channelopathies. What is the meaning of carrying a genetic mutation?

scientific article published on 31 October 2007

Clinical interpretation of genetic variants in arrhythmogenic right ventricular cardiomyopathy

scientific article

Clinical, electrocardiographic, and electrophysiologic characteristics of patients with a fasciculoventricular pathway: The role of PRKAG2 mutation ⬇️

scientific article published on October 1, 2010

Coexistence of epilepsy and Brugada syndrome in a family with SCN5A mutation.

scientific article published on 25 March 2013

Common variation in fatty acid metabolic genes and risk of incident sudden cardiac arrest

scientific article published on 10 January 2014

Compound heterozygous mutations P336L and I1660V in the human cardiac sodium channel associated with the Brugada syndrome

scientific article

Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort

scientific article published on 14 July 2015

Concomitant Brugada-like and short QT electrocardiogram linked to SCN5A mutation ⬇️

scientific article published on April 11, 2012

Conduction abnormalities in the right ventricular outflow tract in Brugada syndrome detected body surface potential mapping

scientific article published on 01 January 2010

Construction of a high-resolution physical map of the chromosome 10q22-q23 dilated cardiomyopathy locus and analysis of candidate genes

scientific article (publication date: 15 July 2000)

Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome.

scientific article

Correction to: Usefulness of Genetic Testing in Hypertrophic Cardiomyopathy: an Analysis Using Real-World Data

scientific article published on 01 August 2019

Correction: Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic Investigation

scientific article published on 6 February 2017

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]

scientific article published on 20 January 2012

Cryptic 5' splice site activation in SCN5A associated with Brugada syndrome

scientific article published on 09 December 2004

Current electrocardiographic criteria for diagnosis of Brugada pattern: a consensus report

article

De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero.

scientific article published on 18 August 2005

Dealing with biological variation in the Brugada syndrome ⬇️

scientific article published on 01 December 2001

Derivation and validation of REASON: A risk score identifying candidates to screen for peripheral arterial disease using ankle brachial index

scientific article published on 19 November 2010

Determinants of Sudden Cardiac Death in Individuals With the Electrocardiographic Pattern of Brugada Syndrome and No Previous Cardiac Arrest ⬇️

scientific article published on November 17, 2003

Determining the pathogenicity of genetic variants associated with cardiac channelopathies

scientific article

DiBAC₄(3) hits a "sweet spot" for the activation of arterial large-conductance Ca²⁺-activated potassium channels independently of the β₁-subunit.

scientific article published on 29 March 2013

Differences in 12-lead electrocardiogram between symptomatic and asymptomatic Brugada syndrome patients.

scientific article published on 12 December 2007

Differences in twelve-lead electrocardiogram between symptomatic and asymptomatic subjects with short QT interval

scientific article

Do sodium channel proteolytic fragments regulate sodium channel expression?

scientific article published on 18 July 2017

Dominant-negative effect of a mutant cardiac troponin T on cardiac structure and function in transgenic mice ⬇️

scientific article published on October 15, 1998

Dual fatty acid synthase and HER2 signaling blockade shows marked antitumor activity against breast cancer models resistant to anti-HER2 drugs

scientific article

Early Identification of Prolonged QT Interval for Prevention of Sudden Infant Death

scientific article published on 29 July 2021

Effect of Opening a New Catheterization Laboratory on 30-Day and 2-Year Survival Rates in Myocardial Infarction Patients

Electrical Substrate Elimination in 135 Consecutive Patients With Brugada Syndrome.

scientific article published on May 2017

Electroanatomic and Pathologic Right Ventricular Outflow Tract Abnormalities in Patients With Brugada Syndrome

scientific article published on 01 December 2018

Electrocardiogram in Newborns: Beneficial or Not?

scientific article published on 27 June 2019

Electrocardiogram interpretation and class I blocker challenge in Brugada syndrome

scientific article published on 28 August 2006

Electrocardiographic Assessment and Genetic Analysis in Neonates: a Current Topic of Discussion

scientific article published on 01 January 2019

Electrocardiographic changes predicting sudden death in propofol-related infusion syndrome.

scientific article

Electrophysiologic testing predicts events in Brugada syndrome patients

scientific article published on 12 July 2011

Elucidating the Role of K+ Channels during In Vitro Capacitation of Boar Spermatozoa: Do SLO1 Channels Play a Crucial Role? ⬇️

scientific article published on 15 December 2019

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

scientific article published on 7 September 2020

Erratum to: Genetic and toxicologic investigation of Sudden Cardiac Death in a patient with Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) under cocaine and alcohol effects

scientific article published on 01 September 2015

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

scientific article published on 05 July 2019

Experimental Models of Brugada syndrome. ⬇️

scientific article published on 29 April 2019

Expert's opinion

Extra Virgin Olive Oil Contains a Phenolic Inhibitor of the Histone Demethylase LSD1/KDM1A

scientific article published on 19 July 2019

Familial Dilated Cardiomyopathy Caused by a Novel Frameshift in the BAG3 Gene

scientific article

Familial clustering of lone atrial fibrillation in patients with saddleback-type ST-segment elevation in right precordial leads

scientific article published on 22 January 2007

Familial dilated cardiomyopathy: A multidisciplinary entity, from basic screening to novel circulating biomarkers.

scientific article published on 8 November 2016

Familial pseudo-Wolff-Parkinson-White syndrome.

scientific article

Fever and Brugada syndrome

scientific article published on 01 November 2002

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

scientific article published on 9 April 2018

Flecainide in patient with aggressive catecholaminergic polymorphic ventricular tachycardia due to novel RYR2 mutation

scientific article published in August 2014

Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant.

scientific article published on 9 January 2015

Further insights into the effect of quinidine in short QT syndrome caused by a mutation in HERG

scientific article

Gender differences in clinical manifestations of Brugada syndrome.

scientific article published in November 2008

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

scientific article published on 13 June 2018

Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome

scientific article published on 31 July 2015

Genetic Modulation of Brugada Syndrome by a Common Polymorphism

scientific article published on 22 June 2009

Genetic Variants as Sudden-Death Risk Markers in Inherited Arrhythmogenic Syndromes: Personalized Genetic Interpretation

scientific article published on 15 June 2020

Genetic analysis in post-mortem samples with micro-ischemic alterations

scientific article published on 03 January 2017

Genetic analysis, in silico prediction, and family segregation in long QT syndrome

scientific article

Genetic and biophysical basis for bupivacaine-induced ST segment elevation and VT/VF. Anesthesia unmasked Brugada syndrome

scientific article published on 7 July 2006

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome

scientific article

Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case series

scientific article published on 15 August 2014

Genetic and toxicologic investigation of Sudden Cardiac Death in a patient with Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) under cocaine and alcohol effects.

scientific article published on 16 November 2014

Genetic aspects of arrhythmias

scientific article

Genetic bases of arrhythmias ⬇️

scientific article published on 01 April 1998

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

scientific article

Genetic basis of atrial fibrillation

scientific article published on 24 September 2016

Genetic basis of dilated cardiomyopathy.

scientific article

Genetic basis of ventricular arrhythmias

scientific article published on 01 April 2010

Genetic basis of ventricular arrhythmias.

scientific article published on August 2008

Genetic causes of sudden infant death syndrome: a postmortem investigation not to be missed

scientific article published on 01 June 2013

Genetic fate mapping identifies second heart field progenitor cells as a source of adipocytes in arrhythmogenic right ventricular cardiomyopathy

scientific article published on 09 April 2009

Genetic interpretation and clinical translation of minor genes related to Brugada syndrome

scientific article published on 29 March 2019

Genetic investigation of sudden unexpected death in epilepsy cohort by panel target resequencing

scientific article published on 30 September 2015

Genetic testing of candidate genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia

scientific article published on 22 February 2012

Genetic variants of uncertain significance: How to match scientific rigour and standard of proof in sudden cardiac death?

scientific article published on 23 April 2020

Genetics and arrhythmias

scientific article

Genetics and cardiac channelopathies.

scientific article published on May 2010

Genetics of Brugada syndrome

scientific article published on 01 May 2010

Genetics of arrhythmogenic right ventricular cardiomyopathy.

scientific article published on 06 March 2013

Genetics of cardiovascular disease with emphasis on atrial fibrillation

scientific article

Genetics of channelopathies associated with sudden cardiac death

scientific article

Genetics of familial atrial fibrillation

scientific article published on 06 August 2009

Genetics of inherited arrhythmias in pediatrics.

scientific article published on 12 September 2015

Genetics of sudden cardiac death in children and young athletes.

scientific article published on 24 July 2012

Genetics of sudden unexplained death

scientific article published on 7 September 2013

Genetics, ethics and ethnicity

article

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).

scientific article published on August 2011

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).

scientific article published on August 2011

Heart rate variability analysis indicates preictal parasympathetic overdrive preceding seizure-induced cardiac dysrhythmias leading to sudden unexpected death in a patient with epilepsy.

scientific article published on 04 April 2014

High sensitivity of the sheep pulmonary vein antrum to acetylcholine stimulation

scientific article published in May 2008

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

scientific article

Identification of Genetic Alterations, as Causative Genetic Defects in Long QT Syndrome, Using Next Generation Sequencing Technology.

scientific article

Identification of N-terminal protein acetylation and arginine methylation of the voltage-gated sodium channel in end-stage heart failure human heart

scientific article published on 27 August 2014

Identification of a genetic locus for familial atrial fibrillation

scientific article

Impacto de la apertura de un nuevo laboratorio de hemodinámica sobre la supervivencia a 30 días y a 2 años en los pacientes con infarto de miocardio

scientific article published on 26 January 2011

Incomplete Penetrance and Variable Expressivity: Hallmarks in Channelopathies Associated with Sudden Cardiac Death

scientific article published on 26 December 2017

Increase in sudden death from coronary artery disease in young adults

scientific article

Induced Brugada-type electrocardiogram, a sign for imminent malignant arrhythmias.

scientific article

Inferior and lateral electrocardiographic repolarization abnormalities in Brugada syndrome

scientific article published on 13 February 2009

Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutation

scientific article published on November 2007

Innovations in heart rhythm disturbances: cardiac electrophysiology, arrhythmias, and cardiac pacing.

scientific article published on 30 November 2012

Integration of "Omics" Strategies for Biomarkers Discovery and for the Elucidation of Molecular Mechanisms Underlying Brugada Syndrome

scientific article published on 20 July 2018

Inter-individual variability in right ventricle adaptation after an endurance race

scientific article published on 10 December 2015

Interplay between R513 methylation and S516 phosphorylation of the cardiac voltage-gated sodium channel.

scientific article

Intimal disruption in type B aortic intramural hematoma. Does size matter? A systematic review and meta-analysis

scientific article published on 26 July 2018

Ionic mechanisms responsible for the electrocardiographic phenotype of the Brugada syndrome are temperature dependent

scientific article

Is atrial fibrillation a genetic disease?

scientific article

Juvenile myoclonic epilepsy and Brugada type 1 ECG pattern associated with (a novel) plakophillin 2 mutation

scientific article published on 20 February 2017

KCNE2 modulation of Kv4.3 current and its potential role in fatal rhythm disorders

scientific article

Kir2.3 knock-down decreases IK1 current in neonatal rat cardiomyocytes

scientific article published on 27 May 2008

Lamotrigine induced Brugada-pattern in a patient with genetic epilepsy associated with a novel variant in SCN9A

scientific article published on 09 June 2020

Large Genomic Imbalances in Brugada Syndrome.

scientific article

Letter to the editor on "The epidemiology of infective endocarditis with focus on non-device related right-sided infective endocarditis: A retrospective register-based study in the region of Southern Denmark" by Lassen et al

scientific article published on 04 July 2020

Lidocaine-induced Brugada syndrome phenotype linked to a novel double mutation in the cardiac sodium channel.

scientific article published on 03 July 2008

Lipoprotein lipase gene mutations, plasma lipid levels, progression/regression of coronary atherosclerosis, response to therapy, and future clinical events. Lipoproteins and Coronary Atherosclerosis Study

scientific article published on June 1999

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

scientific article

Loss-of-function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden death.

scientific article published on August 2013

Massive Migration of an Adrenocortical Carcinoma Thrombus

scientific article published on 01 May 2019

Mechanical Chest Compressions and Traumatic Complications in Out-of-hospital Cardiac Arrest. Is There a Price to Pay?

scientific article published on 11 April 2018

Medico-legal perspectives on sudden cardiac death in young athletes

scientific article published on 21 September 2016

Meta-analyses of the association between cytochrome CYP2C19 loss- and gain-of-function polymorphisms and cardiovascular outcomes in patients with coronary artery disease treated with clopidogrel

scientific article published on 21 June 2011

Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11p ⬇️

scientific article published on March 20, 2013

Molecular autopsy in a cohort of infants died suddenly at rest

scientific article published on 31 July 2018

Molecular autopsy of sudden cardiac death (SCD): the challenge of forensic pathologist to the complexity of genomics

scientific article published on 01 December 2005

Molecular biology and atrial fibrillation

scientific article

Molecular biology of atrial fibrillation

scientific article published on April 2004

Molecular disturbance underlies to arrhythmogenic cardiomyopathy induced by transgene content, age and exercise in a truncated PKP2 mouse model

scientific article published on 12 July 2016

Molecular heterogeneity of large-conductance calcium-activated potassium channels in canine intracardiac ganglia.

scientific article published on 27 June 2013

Multiple episodes of ventricular tachycardia induced by silent coronary vasospasm

scientific article

N-Glycosylation of the voltage-gated sodium channel β2 subunit is required for efficient trafficking of NaV1.5/β2 to the plasma membrane

scientific article published on 11 September 2019

Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic Investigation

scientific article

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

scientific article published in May 2003

Negative autopsy and sudden cardiac death.

scientific article published on 16 February 2014

Nestin(+) stem cells independently contribute to neural remodelling of the ischemic heart ⬇️

scientific article published on May 1, 2011

Novel anti-fatty acid synthase compounds with anti-cancer activity in HER2+ breast cancer.

scientific article published on October 2010

Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction

scientific article

Novel mutations in domain I of SCN5A cause Brugada syndrome

scientific article published in April 2002

Number of electrocardiogram leads displaying the diagnostic coved-type pattern in Brugada syndrome: a diagnostic consensus criterion to be revised

scientific article published on 16 March 2010

P335Sudden unexplained death in Catalonia: comprehensive genetic analysis in post-mortem samples

scientific article published on 27 June 2014

Patients With Brugada Syndrome and Implanted Cardioverter-Defibrillators: Long-Term Follow-Up.

scientific article published in October 2017

Personalized Interpretation and Clinical Translation of Genetic Variants Associated With Cardiomyopathies.

scientific article published on 15 May 2019

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

scientific article

Pharmacological and non-pharmacological therapy for arrhythmias in the pediatric population: EHRA and AEPC-Arrhythmia Working Group joint consensus statement

scientific article

Phenotypic characterization of a large European family with Brugada syndrome displaying a sudden unexpected death syndrome mutation in SCN5A:.

scientific article

Phenotypical Manifestations of Mutations in the Genes Encoding Subunits of the Cardiac Sodium Channel ⬇️

scientific article published on April 1, 2011

Plasma microRNAs as biomarkers for Lamin A/C-related dilated cardiomyopathy

scientific article published on 14 July 2018

Platelet glycoprotein IIIa PlA polymorphism and myocardial infarction

scientific article published on 01 October 1996

Post-mortem genetic analysis in juvenile cases of sudden cardiac death.

scientific article published on 14 October 2014

Present Status of Brugada Syndrome: JACC State-of-the-Art Review

scientific article published on 01 August 2018

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

scientific article published on 8 January 2018

Prognostic value of electrophysiologic investigations in Brugada syndrome

scientific article published in September 2001

Proposed diagnostic criteria for the Brugada syndrome

scientific article

Protein arginine methyl transferases-3 and -5 increase cell surface expression of cardiac sodium channel

scientific article

Proteomic identification of putative biomarkers for early detection of sudden cardiac death in a family with a LMNA gene mutation causing dilated cardiomyopathy.

scientific article published on 22 July 2016

Rare Titin (TTN) Variants in Diseases Associated with Sudden Cardiac Death

scientific article published on 27 October 2015

Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes

scientific article published on 05 April 2020

Rebuttal to EP testing does not predict cardiac events in patients with Brugada syndrome ⬇️

scientific article published on July 23, 2011

Recent Advances in Short QT Syndrome

Recommendations for the use of genetic testing in the clinical evaluation of inherited cardiac arrhythmias associated with sudden cardiac death: Canadian Cardiovascular Society/Canadian Heart Rhythm Society joint position paper

scientific article

Reply to letter to editor: "Genetic basis of dilated cardiomyopathy"

scientific article published on 29 November 2016

Right bundle-branch block and ST-segment elevation in leads V1 through V3: a marker for sudden death in patients without demonstrable structural heart disease

scientific article published in February 1998

Role of candidate modifier genes on the phenotypic expression of hypertrophy in patients with hypertrophic cardiomyopathy

scientific article published on December 1, 1997

Role of copy number variants in sudden cardiac death and related diseases: genetic analysis and translation into clinical practice

scientific article published on 06 March 2018

Role of genetic and electrolyte abnormalities in prolonged QTc interval and sudden cardiac death in end-stage renal disease patients.

scientific article published on 18 July 2018

Role of genetic testing in arrhythmogenic right ventricular cardiomyopathy/dysplasia

scientific article published on 15 October 2009

Role of molecular biology in identifying individuals at risk for sudden cardiac death

scientific article

Role of novel DSP_p.Q986X genetic variation in arrhythmogenic right ventricular cardiomyopathy

scientific article published on 14 August 2013

SCN5A mutation associated with acute myocardial infarction

scientific article

Sarcomeric gene mutations in sudden infant death syndrome (SIDS).

scientific article

Sequenom MassARRAY approach in the arrhythmogenic right ventricular cardiomyopathy post-mortem setting: clinical and forensic implications

scientific article published on 16 May 2014

Shocking truths about implantable cardioverter defibrillator monitoring zones

scientific article published in September 2007

Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants

scientific article published on 16 July 2019

Short QT and atrial fibrillation: A KCNQ1 mutation-specific disease. Late follow-up in three unrelated children.

scientific article

Short QT syndrome

scientific article published on 01 November 2005

Short QT syndrome and atrial fibrillation caused by mutation in KCNH2.

scientific article published in April 2005

Short QT syndrome in pediatrics

scientific article published on 16 March 2017

Short QT syndrome: Should we push the frontier forward?

scientific article published in October 2005

Short QT syndrome: pharmacological treatment

scientific article

Simultaneous ST-segment elevation in the right precordial and inferior leads in Brugada syndrome.

scientific article published in March 2007

Single nucleotide polymorphisms and life-threatening arrhythmias: causal or casual?

scientific article published in November 2001

Sodium channel blockers identify risk for sudden death in patients with ST-segment elevation and right bundle branch block but structurally normal hearts

scientific article

Sodium channel current loss of function in induced pluripotent stem cell-derived cardiomyocytes from a Brugada syndrome patient.

scientific article published on 9 October 2017

Soria Cardioprotegida. The First Spanish Program for the Prevention and Integral Treatment of Sudden Cardiac Death. Response

scientific article published on 06 June 2018

Spatiotemporal Characteristics of QRS Complexes Enable the Diagnosis of Brugada Syndrome Regardless of the Appearance of a Type 1 ECG.

scientific article published on 9 March 2016

State of the art in forensic investigation of sudden cardiac death

scientific article published on March 2011

Stop-gain mutations in PKP2 are associated with a later age of onset of arrhythmogenic right ventricular cardiomyopathy

scientific article

Subcellular localisation of retromer in post-endocytic pathways of polarised Madin-Darby canine kidney cells

scientific article

Sudden Arrhythmic Death During Exercise: A Post-Mortem Genetic Analysis.

scientific article

Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?

scientific article published on 20 March 2020

Sudden death (VI). The Brugada syndrome and right myocardiopathies as a cause of sudden death. The differences and similarities

scientific article

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

scientific article

Sudden death due to catecholaminergic polymorphic ventricular tachycardia following negative stress-test outcome: genetics and clinical implications

scientific article published on 13 April 2017

Sudden death in high-risk family members: Brugada syndrome

scientific article published on 01 November 2000

Sudden death in patients and relatives with the syndrome of right bundle branch block, ST segment elevation in the precordial leads V(1)to V(3)and sudden death

scientific article

Sudden death in structurally normal heart: we have learned a lot, but still a long way to go

scientific article published on 14 September 2015

Sudden death: managing the family, the role of genetics ⬇️

scientific article published on 01 April 2011

Sudden infant death syndrome caused by cardiac arrhythmias: only a matter of genes encoding ion channels?

scientific article published on 12 February 2016

Syndrome of right bundle branch block, ST segment evaluation from V1 to V3 and sudden cardiac death ⬇️

scientific article published on 01 March 1998

T-Wave morphology in short QT syndrome

scientific article published on 01 July 2009

Targeted next-generation sequencing provides novel clues for associated epilepsy and cardiac conduction disorder/SUDEP.

scientific article published on 19 December 2017

The Brugada Syndrome

The Brugada Syndrome

scientific article published on 01 February 2005

The Brugada syndrome

scientific article

The Brugada syndrome

scientific article published on 01 November 2000

The Brugada syndrome

scientific article published on 01 January 2001

The Girona Territori Cardioprotegit Project: Performance Evaluation of Public Defibrillators.

scientific article published on 15 May 2017

The ajmaline challenge in Brugada syndrome: a useful tool or misleading information?

scientific article

The arrhythmogenic right ventricular cardiomyopathy in comparison to the athletic heart

scientific article published on 04 May 2020

The cardiac sodium channel is post-translationally modified by arginine methylation.

scientific article

The cloning, genomic organization and tissue expression profile of the human DLG5 gene

scientific article

The cloning, genomic organization and tissue expression profile of the human DLG5 gene: Correction

scientific article

The long-QT syndrome and exercise practice: The never-ending debate.

scientific article published on 2 January 2018

The molecular genetics of arrhythmias and sudden death

scientific article

The phenotype and potential origin of nestin+ cardiac myocyte-like cells following infarction

scientific article published on 13 August 2009

The puzzle behind electrical chaos and sudden cardiac death in the structurally normal heart

scientific article published on 01 March 1999

The rat heart contains a neural stem cell population; role in sympathetic sprouting and angiogenesis

scientific article

The role of clinical assessment and electrophysiology study in Brugada syndrome patients with syncope

scientific article published on 08 November 2019

The role of clinical, genetic and segregation evaluation in sudden infant death.

scientific article

The smooth muscle-type β1 subunit potentiates activation by DiBAC4(3) in recombinant BK channels.

scientific article published on 3 December 2013

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

scientific article

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

scientific article published on 01 January 2002

The yet unresolved dilemma of syncope in Brugada syndrome

scientific article published in April 2001

The «De Winter» pattern on the electrocardiogram: It is time to run

scientific article published on 07 June 2018

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

Trafficking and Function of the Voltage-Gated Sodium Channel β2 Subunit

scientific article published on 13 October 2019

Trafficking and localisation to the plasma membrane of Nav 1.5 promoted by the β2 subunit is defective due to a β2 mutation associated with Brugada syndrome.

scientific article published on 09 June 2017

Transcriptional regulation of the sodium channel gene (SCN5A) by GATA4 in human heart

scientific article published on 25 November 2016

Trends in Q-wave acute myocardial infarction case fatality from 1978 to 2007 and analysis of the effectiveness of different treatments.

scientific article

Unmasking the molecular link between arrhythmogenic cardiomyopathy and Brugada syndrome

scientific article

Update about atrial fibrillation genetics.

scientific article published on 4 February 2017

Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic?

scientific article published on 28 September 2020

Update on the Genetic Basis of Sudden Unexpected Death in Epilepsy

scientific article published on 23 April 2019

Use of intravenous antiarrhythmics to identify concealed Brugada syndrome

scientific article

Use of the prophylactic implantable cardioverter defibrillator for patients with normal hearts

scientific article

Usefulness of Genetic Testing in Hypertrophic Cardiomyopathy: an Analysis Using Real-World Data

scientific article

Validation of warfarin pharmacogenetic algorithms in clinical practice

scientific article published in January 2012

Value of electrocardiographic parameters and ajmaline test in the diagnosis of Brugada syndrome caused by SCN5A mutations

scientific article

Variability of the diagnostic ECG pattern in an ICD patient population with Brugada syndrome

scientific article published on 04 September 2008

When our best is not enough: the death of a teenager with Brugada syndrome

scientific article published on 25 July 2008

Which ventricular tachycardia is dangerous?

scientific article published in January 1992

Whole-Brain Dynamics in Aging: Disruptions in Functional Connectivity and the Role of the Rich Club

scientific article published on 22 December 2020

Wolff-Parkinson-White Syndrome with Ventricular Hypertrophy in a Brazilian Family

scientific article published on 10 July 2017

[Arrhythmogenic dysplasia of the right ventricle]

scientific article published on 01 August 1997

[Familial auricular fibrillation]

scientific article published on 01 August 1997

[Genetics and arrhythmias]

scientific article published on 01 April 2002

[Molecular biology for the clinical cardiologist: from an entelchy to a necessity]

scholarly article by R Brugada published in January 2001

[ST segment elevation, right bundle branch block and sudden death: Brugada's syndrome].

scientific article

[Same genotype and different phenotypes in a family with PRKAG2 gene mutation]

scientific article published on 01 June 2007

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