Esperanza Molina-Garcia
Murcia, MU, Spain
Last Updated: 09/26/2026
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Found 9 publications
Diagnostic delay and outcome in immunocompetent patients with primary central nervous system lymphoma in Spain: a multicentric study.
Journal: Journal of neuro-oncology
Published: April 01, 2020
A study of the pathogenicity of variants in familial heart disease. The value of cosegregation.
Journal: American journal of translational research
Published: May 04, 2018
Value of the "Standing Test" in the Diagnosis and Evaluation of Beta-blocker Therapy Response in Long QT Syndrome.
Journal: Revista espanola de cardiologia (English ed.)
Published: August 08, 2016
Unclassifiable arrhythmic cardiomyopathy associated with Emery-Dreifuss caused by a mutation in FHL1.
Journal: Clinical genetics
Published: January 11, 2016
An R1632C variant in the SCN5A gene causing Brugada syndrome.
Journal: Molecular medicine reports
Published: October 20, 2014
Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing.
Journal: Revista espanola de cardiologia (English ed.)
Published: August 09, 2014
A study of the SCN5A gene in a cohort of 76 patients with Brugada syndrome.
Journal: Clinical genetics
Published: June 22, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026