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

Valentina Favalli

Showing results (11-20 of 48) with videos related to

Pageof 5
Sort By:
Biochemical and Biophysical Research Communications|January 24, 2012
Structures of the lamin A/C R335W and E347K mutants: implications for dilated cardiolaminopathiesMichela Bollati, Alberto Barbiroli, Valentina Favalli, 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|August 16, 2013
The need to modify patient selection to improve the benefits of implantable cardioverter-defibrillator for primary prevention of sudden death in non-ischaemic dilated cardiomyopathyMarcello Disertori, Silvia Quintarelli, Silvia Mazzola, et al.
Journal of the American College of Cardiology|November 17, 2018
Cardiac Phenotypes in Hereditary Muscle Disorders: JACC State-of-the-Art ReviewEloisa Arbustini, Alessandro Di Toro, Lorenzo Giuliani, et al.
European Journal of Medical Genetics|January 17, 2020
Renal and brain complications in GLA p.Phe113Leu Fabry disease. Comments on "Fabry disease caused by the GLA p.Phe113Leu (p.F113L) variant: Natural history in males" by Oliveira et al. (Eur. J. Med. Genet. 2019)Alexandra Smirnova, Alessandro Di Toro, Lorenzo Giuliani, et al.
European Heart Journal Supplements : Journal of the European Society of Cardiology|April 6, 2019
Genetics and clinics: current applications, limitations, and future developmentsAlessandro Di Toro, Lorenzo Giuliani, Valentina Favalli, et al.
American Journal of Human Genetics|March 24, 2021
Machine learning-based reclassification of germline variants of unknown significance: The RENOVO algorithmValentina Favalli, Giulia Tini, Emanuele Bonetti, et al.
European Heart Journal Supplements : Journal of the European Society of Cardiology|March 3, 2021
Myths to debunk: the non-compacted myocardiumAlessandro Di Toro, Lorenzo Giuliani, Alexandra Smirnova, et al.
Studies in Health Technology and Informatics|September 7, 2011
Information technology solutions to support translational research on inherited cardiomyopathiesRiccardo Bellazzi, Cristiana Larizza, Matteo Gabetta, et al.
European Heart Journal Supplements : Journal of the European Society of Cardiology|June 12, 2020
Hereditary muscle diseases and the heart: the cardiologist's perspectiveLorenzo Giuliani, Alessandro Di Toro, Mario Urtis, et al.
Journal of the American College of Cardiology|October 22, 2016
Cardio-Oncology: The Carney Complex Type IAlessandra Serio, Valentina Favalli, Lorenzo Giuliani, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
Biochemical and Biophysical Research Communications|January 24, 2012
Structures of the lamin A/C R335W and E347K mutants: implications for dilated cardiolaminopathiesMichela Bollati, Alberto Barbiroli, Valentina Favalli, 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|August 16, 2013
The need to modify patient selection to improve the benefits of implantable cardioverter-defibrillator for primary prevention of sudden death in non-ischaemic dilated cardiomyopathyMarcello Disertori, Silvia Quintarelli, Silvia Mazzola, et al.
Journal of the American College of Cardiology|November 17, 2018
Cardiac Phenotypes in Hereditary Muscle Disorders: JACC State-of-the-Art ReviewEloisa Arbustini, Alessandro Di Toro, Lorenzo Giuliani, et al.
European Journal of Medical Genetics|January 17, 2020
Renal and brain complications in GLA p.Phe113Leu Fabry disease. Comments on "Fabry disease caused by the GLA p.Phe113Leu (p.F113L) variant: Natural history in males" by Oliveira et al. (Eur. J. Med. Genet. 2019)Alexandra Smirnova, Alessandro Di Toro, Lorenzo Giuliani, et al.
European Heart Journal Supplements : Journal of the European Society of Cardiology|April 6, 2019
Genetics and clinics: current applications, limitations, and future developmentsAlessandro Di Toro, Lorenzo Giuliani, Valentina Favalli, et al.
American Journal of Human Genetics|March 24, 2021
Machine learning-based reclassification of germline variants of unknown significance: The RENOVO algorithmValentina Favalli, Giulia Tini, Emanuele Bonetti, et al.
European Heart Journal Supplements : Journal of the European Society of Cardiology|March 3, 2021
Myths to debunk: the non-compacted myocardiumAlessandro Di Toro, Lorenzo Giuliani, Alexandra Smirnova, et al.
Studies in Health Technology and Informatics|September 7, 2011
Information technology solutions to support translational research on inherited cardiomyopathiesRiccardo Bellazzi, Cristiana Larizza, Matteo Gabetta, et al.
European Heart Journal Supplements : Journal of the European Society of Cardiology|June 12, 2020
Hereditary muscle diseases and the heart: the cardiologist's perspectiveLorenzo Giuliani, Alessandro Di Toro, Mario Urtis, et al.
Journal of the American College of Cardiology|October 22, 2016
Cardio-Oncology: The Carney Complex Type IAlessandra Serio, Valentina Favalli, Lorenzo Giuliani, et al.
Pageof 5