Visualitzant per matèria "Brugada, Síndrome de"

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

Brugada syndrome and p.E61X_RANGRF

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

Brugada Syndrome and PKP2: Evidences and uncertainties

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

Characterization of non-coding genetic vairants associated with Brugada Syndrome: research and communication

TFC/TFG open access ​

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The utility of implantable loop recorder in the clinical management of pediatric patient with non-high-risk Brugada syndrome

TFC/TFG open access ​

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

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

Experimental models of Brugada syndrome

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

Role of Non-Coding Variants in Brugada Syndrome

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

Sudden Death without a Clear Cause after Comprehensive Investigation: An Example of Forensic Approach to Atypical/Uncertain Findings

Brugada Syndrome in Women: What Do We Know After 30 Years?

Caracterització de variants de significat incert situades al gen codificant pel canal de sodi cardíac en cèl·lules HEK-293T

TFC/TFG open access ​

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