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Forensic Science, Medicine, and Pathology
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April 14, 2017
Sudden death due to catecholaminergic polymorphic ventricular tachycardia following negative stress-test outcome: genetics and clinical implications
Cristian D'Ovidio, Aldo Carnevale, Vincenzo M Grassi, et al.
Biomedicines
|
January 21, 2022
Clinical Genetics of Inherited Arrhythmogenic Disease in the Pediatric Population
Estefanía Martínez-Barrios, Sergi Cesar, José Cruzalegui, et al.
Journal of Cardiovascular Electrophysiology
|
January 28, 2005
Further insights into the effect of quinidine in short QT syndrome caused by a mutation in HERG
Christian Wolpert, Rainer Schimpf, Carla Giustetto, et al.
Diagnostics (Basel, Switzerland)
|
June 2, 2021
Sudden Death without a Clear Cause after Comprehensive Investigation: An Example of Forensic Approach to Atypical/Uncertain Findings
Simone Grassi, Mònica Coll Vidal, Oscar Campuzano, et al.
Stem Cell Research
|
June 30, 2022
Generation of four induced pluripotent stem cell lines from a family harboring a single nucleotide variant in SCN5A
Rebecca Martínez-Moreno, David Carreras, Begoña Aran, et al.
Stem Cell Research
|
November 3, 2023
Generation of the induced pluripotent stem cell line ESi108-A from a familial atrial fibrillation patient
Rebecca Martínez-Moreno, Alexandra Pérez-Serra, Elisabet Selga, et al.
Molecular Genetics and Metabolism
|
June 8, 2002
Novel mutations in domain I of SCN5A cause Brugada syndrome
Matteo Vatta, Robert Dumaine, Charles Antzelevitch, et al.
Channels (Austin, Tex.)
|
June 29, 2013
Molecular heterogeneity of large-conductance calcium-activated potassium channels in canine intracardiac ganglia
Elisabet Selga, Alexandra Pérez-Serra, Alba Moreno-Asso, et al.
Circulation
|
April 9, 2008
Induced Brugada-type electrocardiogram, a sign for imminent malignant arrhythmias
M Juhani Junttila, Maday Gonzalez, Eric Lizotte, et al.
Heart Rhythm
|
March 26, 2014
A missense mutation in the sodium channel β1b subunit reveals SCN1B as a susceptibility gene underlying long QT syndrome
Helena Riuró, Oscar Campuzano, Elena Arbelo, et al.
Page
of 34
Search research articles
Search
Showing results (151-160 of 332) with videos related to
Sort By:
Page
of 34
Forensic Science, Medicine, and Pathology
|
April 14, 2017
Sudden death due to catecholaminergic polymorphic ventricular tachycardia following negative stress-test outcome: genetics and clinical implications
Cristian D'Ovidio, Aldo Carnevale, Vincenzo M Grassi, et al.
Biomedicines
|
January 21, 2022
Clinical Genetics of Inherited Arrhythmogenic Disease in the Pediatric Population
Estefanía Martínez-Barrios, Sergi Cesar, José Cruzalegui, et al.
Journal of Cardiovascular Electrophysiology
|
January 28, 2005
Further insights into the effect of quinidine in short QT syndrome caused by a mutation in HERG
Christian Wolpert, Rainer Schimpf, Carla Giustetto, et al.
Diagnostics (Basel, Switzerland)
|
June 2, 2021
Sudden Death without a Clear Cause after Comprehensive Investigation: An Example of Forensic Approach to Atypical/Uncertain Findings
Simone Grassi, Mònica Coll Vidal, Oscar Campuzano, et al.
Stem Cell Research
|
June 30, 2022
Generation of four induced pluripotent stem cell lines from a family harboring a single nucleotide variant in SCN5A
Rebecca Martínez-Moreno, David Carreras, Begoña Aran, et al.
Stem Cell Research
|
November 3, 2023
Generation of the induced pluripotent stem cell line ESi108-A from a familial atrial fibrillation patient
Rebecca Martínez-Moreno, Alexandra Pérez-Serra, Elisabet Selga, et al.
Molecular Genetics and Metabolism
|
June 8, 2002
Novel mutations in domain I of SCN5A cause Brugada syndrome
Matteo Vatta, Robert Dumaine, Charles Antzelevitch, et al.
Channels (Austin, Tex.)
|
June 29, 2013
Molecular heterogeneity of large-conductance calcium-activated potassium channels in canine intracardiac ganglia
Elisabet Selga, Alexandra Pérez-Serra, Alba Moreno-Asso, et al.
Circulation
|
April 9, 2008
Induced Brugada-type electrocardiogram, a sign for imminent malignant arrhythmias
M Juhani Junttila, Maday Gonzalez, Eric Lizotte, et al.
Heart Rhythm
|
March 26, 2014
A missense mutation in the sodium channel β1b subunit reveals SCN1B as a susceptibility gene underlying long QT syndrome
Helena Riuró, Oscar Campuzano, Elena Arbelo, et al.
Page
of 34