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Molecular Medicine Reports|April 16, 2016
An R1632C variant in the SCN5A gene causing Brugada syndromeEsperanza García-Molina, María Sabater-Molina, Carmen Muñoz, et al.
The American Journal of Emergency Medicine|June 6, 2009
Heat stroke, an unusual trigger of Brugada electrocardiogramJavier Lacunza, Irene San Román, Sara Moreno, et al.
American Journal of Translational Research|April 12, 2019
A study of the pathogenicity of variants in familial heart disease. The value of cosegregationEsperanza García-Molina, María Sabater-Molina, David López-Cuenca, et al.
The American Journal of Cardiology|July 21, 2009
Penetrance and risk profile in inherited cardiac diseases studied in a dedicated screening clinicJuan R Gimeno, Javier Lacunza, Arcadi García-Alberola, et al.
Revista Espanola De Cardiologia (English Ed.)|March 31, 2015
Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic TestingCarmen Muñoz-Esparza, Esperanza García-Molina, Mariela Salar-Alcaraz, et al.
Heart (British Cardiac Society)|November 20, 2010
Insights into genotype-phenotype correlation in hypertrophic cardiomyopathy. Findings from 18 Spanish families with a single mutation in MYBPC3M José Oliva-Sandoval, Francisco Ruiz-Espejo, Lorenzo Monserrat, et al.
Revista Espanola De Cardiologia (English Ed.)|July 9, 2017
Factors Influencing the Phenotypic Expression of Hypertrophic Cardiomyopathy in Genetic CarriersInmaculada Pérez-Sánchez, Antonio José Romero-Puche, Esperanza García-Molina Sáez, et al.
Revista Espanola De Cardiologia (English Ed.)|December 29, 2016
A Novel Founder Mutation in MYBPC3: Phenotypic Comparison With the Most Prevalent MYBPC3 Mutation in SpainMaría Sabater-Molina, Daniel Saura, Esperanza García-Molina Sáez, et al.
Revista Espanola De Cardiologia (English Ed.)|February 25, 2017
Value of the "Standing Test" in the Diagnosis and Evaluation of Beta-blocker Therapy Response in Long QT SyndromeCarmen Muñoz-Esparza, Esther Zorio, Diana Domingo Valero, et al.
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