Browsing by Author "Brugada, Ramon"
orcId Brugada, Ramon​ ​ scopusId Brugada, Ramon​ ​

L'Assistència del pacient i els nous estudis de medicina

Cont. press open access ​

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Experiència d'implementació de l'Aprenentatge Basat en Problemes (ABP) al primer curs dels estudis de medicina en una facultat de nova creació

Autogestión en el proceso de aprendizaje: el viaje a itaca

Análisis de las actividades de evaluación enmarcadas en el método ABP

A Novel Missense Mutation, I890T, in the Pore Region of Cardiac Sodium Channel Causes Brugada Syndrome

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

Characterization of clinical and electrocardiographic findings in a youth population

DFP open access ​

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Association of early repolarization with risk of cardiac mortality in the general population

DFP open access ​

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

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

Stop-Gain Mutations in PKP2 Are Associated with a Later Age of Onset of Arrhythmogenic Right Ventricular Cardiomyopathy

La proyección macular, un nuevo método para determinar la agudeza visual potencial

Thesis open access ​

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El paper de les subunitats beta en la regulació del canal de sodi cardíac associat a la mort sobtada

Thesis open access ​

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

Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort

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

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

Outcomes of a public access defibrillation program in Girona: a cross sectional study

DFP open access ​

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Rare titin (TTN) variants in diseases associated with sudden cardiac death

Determining the Pathogenicity of Genetic Variants Associated with Cardiac Channelopathies

Genetics of channelopathies associated with sudden cardiac death

Variantes genéticas y su relación con la progresión y el pronóstico de la cardiopatía isquémica

Thesis open access ​

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Prevalence of QTc alterations in neonates: age and genetic determinants: end of term project

DFP open access ​

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Paper de la placofilina-2 en la miocardiopatia aritmogènica de ventricle dret: bases genètiques i mecanismes moleculars

Thesis open access ​

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