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Lia Crotti

Showing results (121-130 of 246) with videos related to

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JACC. Clinical Electrophysiology|October 10, 2024
Clinical Features, Long-Term Prognosis, and Clinical Management of Genotype-Negative Long QT Syndrome PatientsKeiko Shimamoto, Federica Dagradi, Seiko Ohno, et al.
Journal of the American College of Cardiology|July 31, 2012
Spectrum and prevalence of mutations involving BrS1- through BrS12-susceptibility genes in a cohort of unrelated patients referred for Brugada syndrome genetic testing: implications for genetic testingLia Crotti, Cherisse A Marcou, David J Tester, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|March 18, 2026
CALM1, CALM2, and CALM3 expression and translation efficiency provide insight into the severity of calmodulinopathySteffan Noe Niikanoff Christiansen, Stine Bøttcher Jacobsen, Jeppe Dyrberg Andersen, et al.
British Journal of Pharmacology|April 16, 2020
The role of mitochondrial dynamics in cardiovascular diseasesMaurizio Forte, Leonardo Schirone, Pietro Ameri, et al.
Heart Rhythm|February 18, 2012
Torsades de pointes following acute myocardial infarction: evidence for a deadly link with a common genetic variantLia Crotti, Dan Hu, Hector Barajas-Martinez, et al.
Circulation. Genomic and Precision Medicine|November 16, 2020
Prevalence and Phenotypic Correlations of Calmodulinopathy-Causative <i>CALM1-3</i> Variants Detected in a Multicenter Molecular Autopsy Cohort of Sudden Unexplained Death VictimsDaniel J Clemens, Belinda Gray, Richard D Bagnall, et al.
International Journal of Cardiology|August 3, 2019
Prevalence of cardiac amyloidosis among adult patients referred to tertiary centres with an initial diagnosis of hypertrophic cardiomyopathyNiccolò Maurizi, Valeria Rella, Carlo Fumagalli, et al.
European Journal of Internal Medicine|October 20, 2023
ECG/echo indexes in the diagnostic approach to amyloid cardiomyopathy: A head-to-head comparison from the AC-TIVE studyLinda Pagura, Aldostefano Porcari, Matteo Cameli, et al.
International Journal of Cardiology|March 19, 2022
Syncope in hypertrophic cardiomyopathy (part I): An updated systematic review and meta-analysisGiuseppe Mascia, Lia Crotti, Antonella Groppelli, et al.
Heart Rhythm|June 19, 2010
Gain-of-function mutation S422L in the KCNJ8-encoded cardiac K(ATP) channel Kir6.1 as a pathogenic substrate for J-wave syndromesArgelia Medeiros-Domingo, Bi-Hua Tan, Lia Crotti, et al.
Pageof 25

Showing results (121-130 of 246) with videos related to

Sort By:
Pageof 25
JACC. Clinical Electrophysiology|October 10, 2024
Clinical Features, Long-Term Prognosis, and Clinical Management of Genotype-Negative Long QT Syndrome PatientsKeiko Shimamoto, Federica Dagradi, Seiko Ohno, et al.
Journal of the American College of Cardiology|July 31, 2012
Spectrum and prevalence of mutations involving BrS1- through BrS12-susceptibility genes in a cohort of unrelated patients referred for Brugada syndrome genetic testing: implications for genetic testingLia Crotti, Cherisse A Marcou, David J Tester, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|March 18, 2026
CALM1, CALM2, and CALM3 expression and translation efficiency provide insight into the severity of calmodulinopathySteffan Noe Niikanoff Christiansen, Stine Bøttcher Jacobsen, Jeppe Dyrberg Andersen, et al.
British Journal of Pharmacology|April 16, 2020
The role of mitochondrial dynamics in cardiovascular diseasesMaurizio Forte, Leonardo Schirone, Pietro Ameri, et al.
Heart Rhythm|February 18, 2012
Torsades de pointes following acute myocardial infarction: evidence for a deadly link with a common genetic variantLia Crotti, Dan Hu, Hector Barajas-Martinez, et al.
Circulation. Genomic and Precision Medicine|November 16, 2020
Prevalence and Phenotypic Correlations of Calmodulinopathy-Causative <i>CALM1-3</i> Variants Detected in a Multicenter Molecular Autopsy Cohort of Sudden Unexplained Death VictimsDaniel J Clemens, Belinda Gray, Richard D Bagnall, et al.
International Journal of Cardiology|August 3, 2019
Prevalence of cardiac amyloidosis among adult patients referred to tertiary centres with an initial diagnosis of hypertrophic cardiomyopathyNiccolò Maurizi, Valeria Rella, Carlo Fumagalli, et al.
European Journal of Internal Medicine|October 20, 2023
ECG/echo indexes in the diagnostic approach to amyloid cardiomyopathy: A head-to-head comparison from the AC-TIVE studyLinda Pagura, Aldostefano Porcari, Matteo Cameli, et al.
International Journal of Cardiology|March 19, 2022
Syncope in hypertrophic cardiomyopathy (part I): An updated systematic review and meta-analysisGiuseppe Mascia, Lia Crotti, Antonella Groppelli, et al.
Heart Rhythm|June 19, 2010
Gain-of-function mutation S422L in the KCNJ8-encoded cardiac K(ATP) channel Kir6.1 as a pathogenic substrate for J-wave syndromesArgelia Medeiros-Domingo, Bi-Hua Tan, Lia Crotti, et al.
Pageof 25