Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Lia Crotti

Showing results (101-110 of 246) with videos related to

Pageof 25
Sort By:
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|July 15, 2025
TP-fusion at peak exercise: a novel marker for the recognition of unsuspected long QT syndrome patientsCarlo Boeri, Patrizio Sarto, Paolo Cerea, et al.
The New England Journal of Medicine|May 9, 2008
Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardiaArthur A M Wilde, Zahurul A Bhuiyan, Lia Crotti, et al.
Circulation|January 11, 2007
Prevalence of long-QT syndrome gene variants in sudden infant death syndromeMarianne Arnestad, Lia Crotti, Torleiv O Rognum, et al.
Stem Cell Research|April 21, 2018
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi002-A from a patient affected by the Jervell and Lange-Nielsen syndrome and carrier of two compound heterozygous mutations on the KCNQ1 geneManuela Mura, Yee-Ki Lee, Monia Ginevrino, et al.
Circulation|August 24, 2005
KCNH2-K897T is a genetic modifier of latent congenital long-QT syndromeLia Crotti, Andrew L Lundquist, Roberto Insolia, et al.
International Journal of Cardiology|May 22, 2017
Desmoplakin missense and non-missense mutations in arrhythmogenic right ventricular cardiomyopathy: Genotype-phenotype correlationSilvia Castelletti, Annina S Vischer, Petros Syrris, et al.
Circulation. Cardiovascular Genetics|August 5, 2014
AKAP9 is a genetic modifier of congenital long-QT syndrome type 1Carin P de Villiers, Lize van der Merwe, Lia Crotti, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|October 11, 2013
Refined multiscale entropy analysis of heart period and QT interval variabilities in long QT syndrome type-1 patientsVlasta Bari, Jose F Valencia, Montserrat Vallverdu, et al.
JACC. Clinical Electrophysiology|March 25, 2022
Left Cardiac Sympathetic Denervation for Long QT Syndrome: 50 Years' Experience Provides Guidance for ManagementVeronica Dusi, Luigi Pugliese, Gaetano M De Ferrari, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|February 2, 2023
Molecular mechanisms underlying the beneficial effects of exercise and dietary interventions in the prevention of cardiometabolic diseasesMaurizio Forte, Daniele Rodolico, Pietro Ameri, et al.
Pageof 25

Showing results (101-110 of 246) with videos related to

Sort By:
Pageof 25
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|July 15, 2025
TP-fusion at peak exercise: a novel marker for the recognition of unsuspected long QT syndrome patientsCarlo Boeri, Patrizio Sarto, Paolo Cerea, et al.
The New England Journal of Medicine|May 9, 2008
Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardiaArthur A M Wilde, Zahurul A Bhuiyan, Lia Crotti, et al.
Circulation|January 11, 2007
Prevalence of long-QT syndrome gene variants in sudden infant death syndromeMarianne Arnestad, Lia Crotti, Torleiv O Rognum, et al.
Stem Cell Research|April 21, 2018
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi002-A from a patient affected by the Jervell and Lange-Nielsen syndrome and carrier of two compound heterozygous mutations on the KCNQ1 geneManuela Mura, Yee-Ki Lee, Monia Ginevrino, et al.
Circulation|August 24, 2005
KCNH2-K897T is a genetic modifier of latent congenital long-QT syndromeLia Crotti, Andrew L Lundquist, Roberto Insolia, et al.
International Journal of Cardiology|May 22, 2017
Desmoplakin missense and non-missense mutations in arrhythmogenic right ventricular cardiomyopathy: Genotype-phenotype correlationSilvia Castelletti, Annina S Vischer, Petros Syrris, et al.
Circulation. Cardiovascular Genetics|August 5, 2014
AKAP9 is a genetic modifier of congenital long-QT syndrome type 1Carin P de Villiers, Lize van der Merwe, Lia Crotti, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|October 11, 2013
Refined multiscale entropy analysis of heart period and QT interval variabilities in long QT syndrome type-1 patientsVlasta Bari, Jose F Valencia, Montserrat Vallverdu, et al.
JACC. Clinical Electrophysiology|March 25, 2022
Left Cardiac Sympathetic Denervation for Long QT Syndrome: 50 Years' Experience Provides Guidance for ManagementVeronica Dusi, Luigi Pugliese, Gaetano M De Ferrari, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|February 2, 2023
Molecular mechanisms underlying the beneficial effects of exercise and dietary interventions in the prevention of cardiometabolic diseasesMaurizio Forte, Daniele Rodolico, Pietro Ameri, et al.
Pageof 25