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Clinical Research in Cardiology : Official Journal of the German Cardiac Society
|
November 16, 2014
Clinical interpretation of genetic variants in arrhythmogenic right ventricular cardiomyopathy
Mireia Alcalde, Oscar Campuzano, Georgia Sarquella-Brugada, et al.
Forensic Science International
|
July 13, 2014
The role of clinical, genetic and segregation evaluation in sudden infant death
Oscar Campuzano, Catarina Allegue, Georgia Sarquella-Brugada, et al.
International Journal of Legal Medicine
|
October 2, 2015
Genetic investigation of sudden unexpected death in epilepsy cohort by panel target resequencing
Monica Coll, Catarina Allegue, Sara Partemi, et al.
Briefings in Bioinformatics
|
July 8, 2024
CARTAR: a comprehensive web tool for identifying potential targets in chimeric antigen receptor therapies using TCGA and GTEx data
Miguel Hernandez-Gamarra, Alba Salgado-Roo, Eduardo Dominguez, et al.
Plos One
|
August 1, 2015
Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome
Catarina Allegue, Mònica Coll, Jesus Mates, et al.
Forensic Science International
|
February 25, 2012
Sarcomeric gene mutations in sudden infant death syndrome (SIDS)
Maria Brion, Catarina Allegue, Montserrat Santori, et al.
Frontiers in Cellular Neuroscience
|
April 25, 2022
Identification of Sodium Transients Through Na<sub>V</sub>1.5 Channels as Regulators of Differentiation in Immortalized Dorsal Root Ganglia Neurons
Antón L Martínez, José Brea, Eduardo Domínguez, et al.
Plos One
|
December 11, 2014
Identification of Genetic Alterations, as Causative Genetic Defects in Long QT Syndrome, Using Next Generation Sequencing Technology
Oscar Campuzano, Georgia Sarquella-Brugada, Irene Mademont-Soler, et al.
International Journal of Molecular Sciences
|
October 31, 2015
Rare Titin (TTN) Variants in Diseases Associated with Sudden Cardiac Death
Oscar Campuzano, Olallo Sanchez-Molero, Irene Mademont-Soler, et al.
Annals of Clinical and Laboratory Science
|
August 7, 2010
Identification of a novel MYBPC3 gene variant in a patient with hypertrophic cardiomyopathy
Maria Brion, Catarina Allegue, Rocio Gil, et al.
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of 4
Search research articles
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Showing results (11-20 of 38) with videos related to
Sort By:
Page
of 4
Clinical Research in Cardiology : Official Journal of the German Cardiac Society
|
November 16, 2014
Clinical interpretation of genetic variants in arrhythmogenic right ventricular cardiomyopathy
Mireia Alcalde, Oscar Campuzano, Georgia Sarquella-Brugada, et al.
Forensic Science International
|
July 13, 2014
The role of clinical, genetic and segregation evaluation in sudden infant death
Oscar Campuzano, Catarina Allegue, Georgia Sarquella-Brugada, et al.
International Journal of Legal Medicine
|
October 2, 2015
Genetic investigation of sudden unexpected death in epilepsy cohort by panel target resequencing
Monica Coll, Catarina Allegue, Sara Partemi, et al.
Briefings in Bioinformatics
|
July 8, 2024
CARTAR: a comprehensive web tool for identifying potential targets in chimeric antigen receptor therapies using TCGA and GTEx data
Miguel Hernandez-Gamarra, Alba Salgado-Roo, Eduardo Dominguez, et al.
Plos One
|
August 1, 2015
Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome
Catarina Allegue, Mònica Coll, Jesus Mates, et al.
Forensic Science International
|
February 25, 2012
Sarcomeric gene mutations in sudden infant death syndrome (SIDS)
Maria Brion, Catarina Allegue, Montserrat Santori, et al.
Frontiers in Cellular Neuroscience
|
April 25, 2022
Identification of Sodium Transients Through Na<sub>V</sub>1.5 Channels as Regulators of Differentiation in Immortalized Dorsal Root Ganglia Neurons
Antón L Martínez, José Brea, Eduardo Domínguez, et al.
Plos One
|
December 11, 2014
Identification of Genetic Alterations, as Causative Genetic Defects in Long QT Syndrome, Using Next Generation Sequencing Technology
Oscar Campuzano, Georgia Sarquella-Brugada, Irene Mademont-Soler, et al.
International Journal of Molecular Sciences
|
October 31, 2015
Rare Titin (TTN) Variants in Diseases Associated with Sudden Cardiac Death
Oscar Campuzano, Olallo Sanchez-Molero, Irene Mademont-Soler, et al.
Annals of Clinical and Laboratory Science
|
August 7, 2010
Identification of a novel MYBPC3 gene variant in a patient with hypertrophic cardiomyopathy
Maria Brion, Catarina Allegue, Rocio Gil, et al.
Page
of 4