Publications by authors named "Rocio Gil"

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Detection of the Copy Number Variants of Genes in Patients with Familial Cardiac Diseases by Massively Parallel Sequencing.
Alejandro Blanco-Verea, Brais Piñeiro, Rocio Gil, Eva Ramos-Luis, María Álvarez-Barredo

Mol Diagn Ther· January 2023

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Potential drug-drug interactions in COVID 19 patients in treatment with lopinavir/ritonavir.
David Brandariz-Nuñez, Marcelo Correas-Sanahuja, Eva Guarc, Rafael Picón, Bárbara García, Rocío Gil

Med Clin (Barc)· October 2020

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Potential drug-drug interactions in COVID 19 patients in treatment with lopinavir/ritonavir.
David Brandariz-Nuñez, Marcelo Correas-Sanahuja, Eva Guarc, Rafael Picón, Bárbara García, Rocío Gil

Med Clin (Engl Ed)· October 2020

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Sudden infant death as the most severe phenotype caused by genetic modulation in a family with atrial fibrillation.
Montserrat Santori, Rocío Gil, Alejandro Blanco-Verea, Helena Riuró, Óscar Díaz-Castro

Forensic Sci Int Genet· November 2019

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Broad-based molecular autopsy: a potential tool to investigate the involvement of subtle cardiac conditions in sudden unexpected death in infancy and early childhood.
Montserrat Santori, Alejandro Blanco-Verea, Rocio Gil, Judith Cortis, Katrin Becker

Arch Dis Child· October 2015

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Next generation sequencing challenges in the analysis of cardiac sudden death due to arrhythmogenic disorders.
Maria Brion, Alejandro Blanco-Verea, Beatriz Sobrino, Montserrat Santori, Rocio Gil

Electrophoresis· November 2014

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Sarcomeric gene mutations in sudden infant death syndrome (SIDS).
Maria Brion, Catarina Allegue, Montserrat Santori, Rocio Gil, Alejandro Blanco-Verea

Forensic Sci Int· June 2012

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Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases.
Catarina Allegue, Rocio Gil, Alejandro Blanco-Verea, Montserrat Santori, Marisol Rodríguez-Calvo

Int J Legal Med· July 2011

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Identification of a novel MYBPC3 gene variant in a patient with hypertrophic cardiomyopathy.
Maria Brion, Catarina Allegue, Rocio Gil, Alejandro Blanco-Verea, Angel Carracedo

Ann Clin Lab Sci· November 2010

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A new approach to long QT syndrome mutation detection by Sequenom MassARRAY system.
Catarina Allegue, Rocio Gil, Paula Sanchez-Diz, María Torres, Inés Quintela

Electrophoresis· May 2010

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