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Electrocardiographic findings in patients with arrhythmogenic cardiomyopathy and right bundle branch block ventricular tachycardia

Europace (London, England), 2023-03, Vol.25 (3), p.1025-1034

2023

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Molecular stratification of arrhythmogenic mechanisms in the Andersen Tawil syndrome

Cardiovascular research, 2023-05, Vol.119 (4), p.919-932

2023

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Prognostic impact of misdiagnosis of cardiac channelopathies as epilepsy

PloS one, 2020-04, Vol.15 (4), p.e0231442

2020

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Absence of relevant QT interval prolongation in not critically ill COVID-19 patients

Scientific reports, 2020-12, Vol.10 (1), p.21417-8, Article 21417

2020

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Layer-Specific Global Longitudinal Strain Predicts Arrhythmic Risk in Arrhythmogenic Cardiomyopathy

Frontiers in cardiovascular medicine, 2021-11, Vol.8, p.748003-748003

2021

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A gain-of-function HCN4 mutant in the HCN domain is responsible for inappropriate sinus tachycardia in a Spanish family

Proceedings of the National Academy of Sciences - PNAS, 2023-12, Vol.120 (49), p.e2305135120-e2305135120

2023

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To the Editor—Mexiletine in myotonic dystrophy: Beware of ventricular arrhythmias

Heart rhythm, 2021-04, Vol.18 (4), p.660-660

2021

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Clinical characteristics and determinants of the phenotype in TMEM43 arrhythmogenic right ventricular cardiomyopathy type 5

Heart rhythm, 2020-06, Vol.17 (6), p.945-954

2020

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Overlap of Arrhythmogenic Cardiomyopathy, Spongiform Cardiomyopathy, and Congenital Heart Disease

Revista española de cardiología (English ed.), 2017-01, Vol.70 (1), p.51-51

2017

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Letter to Editor: Functional study is not the only criterion to predict the pathogenicity of a novel mutation for cardiomyopathy

Journal of molecular and cellular cardiology, 2017-08, Vol.109, p.58-59

2017

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Genotype, Family History, and Outcomes in Noncompaction Cardiomyopathy

Journal of the American College of Cardiology, 2018-06, Vol.71 (24), p.2864-2864

2018

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The prevalence of left and right bundle branch block morphology ventricular tachycardia amongst patients with arrhythmogenic cardiomyopathy and sustained ventricular tachycardia: insights from the European Survey on Arrhythmogenic Cardiomyopathy

Europace (London, England), 2022-02, Vol.24 (2), p.285-295

2022

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Solapamiento de miocardiopatía arritmogénica y espongiforme con cardiopatía congénita

Revista española de cardiologia, 2017-01, Vol.70 (1), p.51-51

2017

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Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion

Journal of clinical medicine, 2021-10, Vol.10 (19), p.4608

2021

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Kir2.1 dysfunction at the sarcolemma and the sarcoplasmic reticulum causes arrhythmias in a mouse model of Andersen–Tawil syndrome type 1

Nature Cardiovascular Research, 2022-10, Vol.1 (10), p.900-917

2022

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Monomorphic and Polymorphic Ventricular Arrhythmias in Heterozygous Calsequestrin-2 Mutation Carriers

Circulation. Genomic and precision medicine, 2022-04, Vol.15 (2), p.e003518

2022

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BS-452757-3 UNRAVELLING THE ARRHYTHMOGENIC MECHANISMS OF SHORT QT SYNDROME TYPE 3 IN AN ANIMAL MODEL OF KIR2.1M301KGAIN-OF-FUNCTION MUTATION

Heart rhythm, 2023-05, Vol.20 (5), p.S54-S54

2023

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Risk predictors in a Spanish cohort with cardiac laminopathies. The REDLAMINA registry

Revista española de cardiología (English ed.), 2021-03, Vol.74 (3), p.216-224

2021

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Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia

Circulation (New York, N.Y.), 2018-04, Vol.137 (15), p.1595-1610

2018

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Regression of Left Ventricular Hypertrophy in a Case of Sarcomeric Hypertrophic Cardiomyopathy

JACC. Case reports, 2020-06, Vol.2 (6), p.935-937

2020

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Giant biventricular aneurysms: a novel cardiac phenotype in myotubular/centronuclear myopathy

European heart journal, 2018-12, Vol.39 (48), p.4289-4290

2018

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Resonancia magnética cardiaca en la miocardiopatía arritmogénica: ¿hay que actualizar los criterios de 2010?

Revista española de cardiologia, 2020-11, Vol.73 (11), p.871-873

2020

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PO-455617-2 UNRAVELLING THE ARRHYTHMOGENIC MECHANISMS OF SHORT QT SYNDROME TYPE 3 IN AN ANIMAL MODEL OF KIR2.1M301K GAIN-OF-FUNCTION MUTATION

Heart rhythm, 2023-05, Vol.20 (5), p.S729-S730

2023

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Electrocardiographic findings in patients with arrhythmogenic cardiomyopathy and right bundle branch block ventricular tachycardia

Molecular stratification of arrhythmogenic mechanisms in the Andersen Tawil syndrome

Prognostic impact of misdiagnosis of cardiac channelopathies as epilepsy

Absence of relevant QT interval prolongation in not critically ill COVID-19 patients

Layer-Specific Global Longitudinal Strain Predicts Arrhythmic Risk in Arrhythmogenic Cardiomyopathy

Extracellular Kir2.1 C122Y Mutant Upsets Kir2.1-PIP 2 Bonds and Is Arrhythmogenic in Andersen-Tawil Syndrome

A gain-of-function HCN4 mutant in the HCN domain is responsible for inappropriate sinus tachycardia in a Spanish family

To the Editor—Mexiletine in myotonic dystrophy: Beware of ventricular arrhythmias

Clinical characteristics and determinants of the phenotype in TMEM43 arrhythmogenic right ventricular cardiomyopathy type 5

Overlap of Arrhythmogenic Cardiomyopathy, Spongiform Cardiomyopathy, and Congenital Heart Disease

Letter to Editor: Functional study is not the only criterion to predict the pathogenicity of a novel mutation for cardiomyopathy

Genotype, Family History, and Outcomes in Noncompaction Cardiomyopathy

The prevalence of left and right bundle branch block morphology ventricular tachycardia amongst patients with arrhythmogenic cardiomyopathy and sustained ventricular tachycardia: insights from the European Survey on Arrhythmogenic Cardiomyopathy

Solapamiento de miocardiopatía arritmogénica y espongiforme con cardiopatía congénita

Prevalence of bleeding secondary to anticoagulation and mortality in patients with atrial fibrillation admitted with SARS-CoV-2 infection

Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion

Kir2.1 dysfunction at the sarcolemma and the sarcoplasmic reticulum causes arrhythmias in a mouse model of Andersen–Tawil syndrome type 1

Monomorphic and Polymorphic Ventricular Arrhythmias in Heterozygous Calsequestrin-2 Mutation Carriers

BS-452757-3 UNRAVELLING THE ARRHYTHMOGENIC MECHANISMS OF SHORT QT SYNDROME TYPE 3 IN AN ANIMAL MODEL OF KIR2.1M301KGAIN-OF-FUNCTION MUTATION

Risk predictors in a Spanish cohort with cardiac laminopathies. The REDLAMINA registry

Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia

Regression of Left Ventricular Hypertrophy in a Case of Sarcomeric Hypertrophic Cardiomyopathy

Giant biventricular aneurysms: a novel cardiac phenotype in myotubular/centronuclear myopathy

Resonancia magnética cardiaca en la miocardiopatía arritmogénica: ¿hay que actualizar los criterios de 2010?

PO-455617-2 UNRAVELLING THE ARRHYTHMOGENIC MECHANISMS OF SHORT QT SYNDROME TYPE 3 IN AN ANIMAL MODEL OF KIR2.1M301K GAIN-OF-FUNCTION MUTATION

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