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Lia Crotti

Showing results (151-160 of 246) with videos related to

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Circulation. Arrhythmia and Electrophysiology|October 16, 2012
A novel disease gene for Brugada syndrome: sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.5Taisuke Ishikawa, Akinori Sato, Cherisse A Marcou, et al.
Circulation|February 15, 2021
Sex-Related Differences in Cardiac Channelopathies: Implications for Clinical PracticeBabken Asatryan, Lauren Yee, Yael Ben-Haim, et al.
Circulation Research|June 26, 2014
Characterization of SEMA3A-encoded semaphorin as a naturally occurring Kv4.3 protein inhibitor and its contribution to Brugada syndromeNicole J Boczek, Dan Ye, Eric K Johnson, et al.
Cardiovascular Research|February 4, 2017
Elucidating arrhythmogenic mechanisms of long-QT syndrome CALM1-F142L mutation in patient-specific induced pluripotent stem cell-derived cardiomyocytesMarcella Rocchetti, Luca Sala, Lisa Dreizehnter, et al.
JACC. Advances|May 4, 2025
Echocardiographic Tissue Characterization Using Radiomics in Patients With Transthyretin-Related Cardiac AmyloidosisSara Mori, Noemi Montobbio, Maria Pia Sormani, et al.
Heart Rhythm|December 14, 2011
A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currentsDan Hu, Hector Barajas-Martínez, Argelia Medeiros-Domingo, et al.
Circulation|November 7, 2007
The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratificationLia Crotti, Carla Spazzolini, Peter J Schwartz, et al.
The Journal of Clinical Investigation|May 3, 2008
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndromeNaomasa Makita, Elijah Behr, Wataru Shimizu, et al.
European Journal of Preventive Cardiology|July 28, 2020
Unexplained sudden cardiac arrest in children: clinical and genetic characteristics of survivorsEmanuele Monda, Berardo Sarubbi, Maria Giovanna Russo, et al.
Circulation|June 28, 2024
Therapeutic Efficacy of Mexiletine for Long QT Syndrome Type 2: Evidence From Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes, Transgenic Rabbits, and PatientsLia Crotti, Raquel Neves, Federica Dagradi, et al.
Pageof 25

Showing results (151-160 of 246) with videos related to

Sort By:
Pageof 25
Circulation. Arrhythmia and Electrophysiology|October 16, 2012
A novel disease gene for Brugada syndrome: sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.5Taisuke Ishikawa, Akinori Sato, Cherisse A Marcou, et al.
Circulation|February 15, 2021
Sex-Related Differences in Cardiac Channelopathies: Implications for Clinical PracticeBabken Asatryan, Lauren Yee, Yael Ben-Haim, et al.
Circulation Research|June 26, 2014
Characterization of SEMA3A-encoded semaphorin as a naturally occurring Kv4.3 protein inhibitor and its contribution to Brugada syndromeNicole J Boczek, Dan Ye, Eric K Johnson, et al.
Cardiovascular Research|February 4, 2017
Elucidating arrhythmogenic mechanisms of long-QT syndrome CALM1-F142L mutation in patient-specific induced pluripotent stem cell-derived cardiomyocytesMarcella Rocchetti, Luca Sala, Lisa Dreizehnter, et al.
JACC. Advances|May 4, 2025
Echocardiographic Tissue Characterization Using Radiomics in Patients With Transthyretin-Related Cardiac AmyloidosisSara Mori, Noemi Montobbio, Maria Pia Sormani, et al.
Heart Rhythm|December 14, 2011
A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currentsDan Hu, Hector Barajas-Martínez, Argelia Medeiros-Domingo, et al.
Circulation|November 7, 2007
The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratificationLia Crotti, Carla Spazzolini, Peter J Schwartz, et al.
The Journal of Clinical Investigation|May 3, 2008
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndromeNaomasa Makita, Elijah Behr, Wataru Shimizu, et al.
European Journal of Preventive Cardiology|July 28, 2020
Unexplained sudden cardiac arrest in children: clinical and genetic characteristics of survivorsEmanuele Monda, Berardo Sarubbi, Maria Giovanna Russo, et al.
Circulation|June 28, 2024
Therapeutic Efficacy of Mexiletine for Long QT Syndrome Type 2: Evidence From Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes, Transgenic Rabbits, and PatientsLia Crotti, Raquel Neves, Federica Dagradi, et al.
Pageof 25