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

Enrico S Bertini

Showing results (1-10 of 21) with videos related to

Pageof 3
Sort By:
Orphanet Journal of Rare Diseases|May 17, 2011
X-linked disorders with cerebellar dysgenesisGinevra Zanni, Enrico S Bertini
Antioxidants (Basel, Switzerland)|November 11, 2022
Antioxidant Response in Human X-Linked Adrenoleukodystrophy FibroblastsSara Petrillo, Jessica D'Amico, Francesco Nicita, et al.
Journal of Neuroimmunology|October 12, 2016
Immune-mediated rippling muscle disease and myasthenia gravisMariela Bettini, Hernan Gonorazky, Marcelo Chaves, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|October 29, 2024
Gene therapy for Duchenne Muscular Dystrophy: assessing the readiness of Italian centres of expertiseMarika Pane, Enrico S Bertini, Eleonora Russo, et al.
Frontiers in Cellular Neuroscience|August 17, 2019
Nrf2 Induction Re-establishes a Proper Neuronal Differentiation Program in Friedreich's Ataxia Neural Stem CellsPiergiorgio La Rosa, Marta Russo, Jessica D'Amico, et al.
International Journal of Rehabilitation Research. Internationale Zeitschrift Fur Rehabilitationsforschung. Revue Internationale De Recherches De Readaptation|July 26, 2018
Longitudinal gait assessment in a stiff person syndromeTommaso Schirinzi, Andrea Sancesario, Alberto Romano, et al.
Archivos Argentinos De Pediatria|November 1, 2017
[Clinical and molecular study in a family with cleidocranial dysplasia]Michele Callea, Fabiana Fattori, Enrico S Bertini, et al.
Journal of Child Neurology|September 1, 2007
Consensus statement for standard of care in spinal muscular atrophyChing H Wang, Richard S Finkel, Enrico S Bertini, et al.
Redox Biology|November 16, 2020
The Nrf2 induction prevents ferroptosis in Friedreich's AtaxiaPiergiorgio La Rosa, Sara Petrillo, Riccardo Turchi, et al.
American Journal of Medical Genetics. Part A|July 23, 2022
Expanding phenotype of FAM111B-related disease focusing on liver involvement: Literature review, report of a case with end-stage liver disease and proposal for a new acronymMarina Macchiaiolo, Filippo M Panfili, Davide Vecchio, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Orphanet Journal of Rare Diseases|May 17, 2011
X-linked disorders with cerebellar dysgenesisGinevra Zanni, Enrico S Bertini
Antioxidants (Basel, Switzerland)|November 11, 2022
Antioxidant Response in Human X-Linked Adrenoleukodystrophy FibroblastsSara Petrillo, Jessica D'Amico, Francesco Nicita, et al.
Journal of Neuroimmunology|October 12, 2016
Immune-mediated rippling muscle disease and myasthenia gravisMariela Bettini, Hernan Gonorazky, Marcelo Chaves, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|October 29, 2024
Gene therapy for Duchenne Muscular Dystrophy: assessing the readiness of Italian centres of expertiseMarika Pane, Enrico S Bertini, Eleonora Russo, et al.
Frontiers in Cellular Neuroscience|August 17, 2019
Nrf2 Induction Re-establishes a Proper Neuronal Differentiation Program in Friedreich's Ataxia Neural Stem CellsPiergiorgio La Rosa, Marta Russo, Jessica D'Amico, et al.
International Journal of Rehabilitation Research. Internationale Zeitschrift Fur Rehabilitationsforschung. Revue Internationale De Recherches De Readaptation|July 26, 2018
Longitudinal gait assessment in a stiff person syndromeTommaso Schirinzi, Andrea Sancesario, Alberto Romano, et al.
Archivos Argentinos De Pediatria|November 1, 2017
[Clinical and molecular study in a family with cleidocranial dysplasia]Michele Callea, Fabiana Fattori, Enrico S Bertini, et al.
Journal of Child Neurology|September 1, 2007
Consensus statement for standard of care in spinal muscular atrophyChing H Wang, Richard S Finkel, Enrico S Bertini, et al.
Redox Biology|November 16, 2020
The Nrf2 induction prevents ferroptosis in Friedreich's AtaxiaPiergiorgio La Rosa, Sara Petrillo, Riccardo Turchi, et al.
American Journal of Medical Genetics. Part A|July 23, 2022
Expanding phenotype of FAM111B-related disease focusing on liver involvement: Literature review, report of a case with end-stage liver disease and proposal for a new acronymMarina Macchiaiolo, Filippo M Panfili, Davide Vecchio, et al.
Pageof 3