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Filamin C missense variant associated with severe right atrial disease and skeletal myopathy

Journal of cardiovascular electrophysiology, 2021-10, Vol.32 (10), p.2777-2780

2021

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Cardiac Channel Molecular Autopsy: Insights From 173 Consecutive Cases of Autopsy-Negative Sudden Unexplained Death Referred for Postmortem Genetic Testing

Mayo Clinic proceedings, 2012-06, Vol.87 (6), p.524-539

2012

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Unexplained Drownings and the Cardiac Channelopathies: A Molecular Autopsy Series

Mayo Clinic proceedings, 2011-10, Vol.86 (10), p.941-947

2011

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Late‐onset severe long QT syndrome

Annals of noninvasive electrocardiology, 2018-07, Vol.23 (4), p.e12517-n/a

2018

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Usefulness of Inducible Ventricular Tachycardia to Predict Long-Term Adverse Outcomes in Arrhythmogenic Right Ventricular Cardiomyopathy

The American journal of cardiology, 2013-01, Vol.111 (2), p.250-257

2013

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Usefulness of Electrocardiographic Parameters for Risk Prediction in Arrhythmogenic Right Ventricular Dysplasia

The American journal of cardiology, 2014-05, Vol.113 (10), p.1728-1734

2014

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Failure rate and conductor externalization in the Biotronik Linox/Sorin Vigila implantable cardioverter-defibrillator lead

Heart rhythm, 2016-05, Vol.13 (5), p.1075-1082

2016

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Sudden cardiac death in forensic medicine – Swiss recommendations for a multidisciplinary approach

Swiss medical weekly, 2015-06, Vol.145, p.w14129

2015

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Recommendations for genetic testing and counselling after sudden cardiac death: practical aspects for Swiss practice

Swiss medical weekly, 2018-07, Vol.148, p.w14638

2018

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Sex hormones affect outcome in arrhythmogenic right ventricular cardiomyopathy/dysplasia: from a stem cell derived cardiomyocyte-based model to clinical biomarkers of disease outcome

European heart journal, 2017-05, Vol.38 (19), p.1498-1508

2017

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Clinical Role of Atrial Arrhythmias in Patients With Arrhythmogenic Right Ventricular Dysplasia

Circulation Journal, 2014/11/25, Vol.78(12), pp.2854-2861

2014

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Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex

Proceedings of the National Academy of Sciences - PNAS, 2008-07, Vol.105 (27), p.9355-9360

2008

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Four TRPM4 Cation Channel Mutations Found in Cardiac Conduction Diseases Lead to Altered Protein Stability

Frontiers in physiology, 2018-03, Vol.9, p.177-177

2018

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SCN4B-encoded sodium channel β4 subunit in congenital long-QT syndrome

Circulation (New York, N.Y.), , Vol.116 (2), p.134-142

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Sports-related sudden cardiac deaths in the young population of Switzerland

PloS one, 2017-03, Vol.12 (3), p.e0174434-e0174434

2017

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Functional characterization of a novel SCN5A variant associated with long QT syndrome and sudden cardiac death

International journal of legal medicine, 2019-11, Vol.133 (6), p.1733-1742

2019

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Spectrum and Prevalence of Mutations Involving BrS1- Through BrS12-Susceptibility Genes in a Cohort of Unrelated Patients Referred for Brugada Syndrome Genetic Testing

Journal of the American College of Cardiology, 2012-10, Vol.60 (15), p.1410-1418

2012

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Brugada Syndrome Associated with Different Heterozygous SCN5A Variants in Two Unrelated Families

Journal of clinical medicine, 2022-09, Vol.11 (19), p.5625

2022

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Catecholaminergic Polymorphic Ventricular Tachycardia: Multiple Clinical Presentations of a Genetically Determined Disease

Journal of clinical medicine, 2023-12, Vol.13 (1), p.47

2023

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Different prognostic value of functional right ventricular parameters in arrhythmogenic right ventricular cardiomyopathy/dysplasia

Circulation. Cardiovascular imaging, 2014-03, Vol.7 (2), p.230-239

2014

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A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currents

Heart rhythm, 2012-05, Vol.9 (5), p.760-769

2012

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Potenciales efectos pro-arrítmicos de la farmacoterapia contra SARS-CoV-2

Archivos de cardiología de México, 2020, Vol.90 (91), p.36-40

2020

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Filamin C missense variant associated with severe right atrial disease and skeletal myopathy

Cardiac Channel Molecular Autopsy: Insights From 173 Consecutive Cases of Autopsy-Negative Sudden Unexplained Death Referred for Postmortem Genetic Testing

Unexplained Drownings and the Cardiac Channelopathies: A Molecular Autopsy Series

Late‐onset severe long QT syndrome

Usefulness of Inducible Ventricular Tachycardia to Predict Long-Term Adverse Outcomes in Arrhythmogenic Right Ventricular Cardiomyopathy

Usefulness of Electrocardiographic Parameters for Risk Prediction in Arrhythmogenic Right Ventricular Dysplasia

Failure rate and conductor externalization in the Biotronik Linox/Sorin Vigila implantable cardioverter-defibrillator lead

Sudden cardiac death in forensic medicine – Swiss recommendations for a multidisciplinary approach

Evidence-Based Assessment of Genes in Dilated Cardiomyopathy

Recommendations for genetic testing and counselling after sudden cardiac death: practical aspects for Swiss practice

Sex hormones affect outcome in arrhythmogenic right ventricular cardiomyopathy/dysplasia: from a stem cell derived cardiomyocyte-based model to clinical biomarkers of disease outcome

Clinical Role of Atrial Arrhythmias in Patients With Arrhythmogenic Right Ventricular Dysplasia

Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex

Four TRPM4 Cation Channel Mutations Found in Cardiac Conduction Diseases Lead to Altered Protein Stability

SCN4B-encoded sodium channel β4 subunit in congenital long-QT syndrome

Sports-related sudden cardiac deaths in the young population of Switzerland

The genetic architecture of Plakophilin 2 cardiomyopathy

Functional characterization of a novel SCN5A variant associated with long QT syndrome and sudden cardiac death

Spectrum and Prevalence of Mutations Involving BrS1- Through BrS12-Susceptibility Genes in a Cohort of Unrelated Patients Referred for Brugada Syndrome Genetic Testing

Brugada Syndrome Associated with Different Heterozygous SCN5A Variants in Two Unrelated Families

Catecholaminergic Polymorphic Ventricular Tachycardia: Multiple Clinical Presentations of a Genetically Determined Disease

Different prognostic value of functional right ventricular parameters in arrhythmogenic right ventricular cardiomyopathy/dysplasia

A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currents

Potenciales efectos pro-arrítmicos de la farmacoterapia contra SARS-CoV-2

Correction to: The genetic architecture of Plakophilin 2 cardiomyopathy

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