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

Francesco Fortunato

Showing results (71-80 of 120) with videos related to

Pageof 12
Sort By:
Journal of the Neurological Sciences|November 13, 2008
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunctionStefania Corti, Chiara Donadoni, Dario Ronchi, et al.
Annals of Clinical and Translational Neurology|April 25, 2020
Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiencyDario Ronchi, Edoardo Monfrini, Sara Bonato, et al.
BMC Neurology|July 14, 2011
Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G>A mitochondrial DNA mutation: a case reportDario Ronchi, Alessandra Cosi, Davide Tonduti, et al.
Human Mutation|August 16, 2005
Mutation finding in patients with dysferlin deficiency and role of the dysferlin interacting proteins annexin A1 and A2 in muscular dystrophiesRachele Cagliani, Francesca Magri, Antonio Toscano, et al.
Plos One|May 3, 2014
Mitochondrial changes in platelets are not related to those in skeletal muscle during human septic shockAlessandro Protti, Francesco Fortunato, Maria L Caspani, et al.
CNS Drugs|February 27, 2025
Exploring the Effectiveness of Adjunctive Cenobamate in Focal Epilepsy: A Time-Based AnalysisRoberta Roberti, Gianfranco Di Gennaro, Vittoria Cianci, et al.
Archives of Neurology|July 14, 2010
Mitochondrial respiratory chain dysfunction in muscle from patients with amyotrophic lateral sclerosisVeronica Crugnola, Costanza Lamperti, Valeria Lucchini, et al.
International Journal of Molecular Sciences|March 29, 2023
Extracellular Matrix Disorganization and Sarcolemmal Alterations in COL6-Related Myopathy Patients with New Variants of COL6 GenesSimona Zanotti, Francesca Magri, Sabrina Salani, et al.
The Journal of Clinical Investigation|September 5, 2008
Neural stem cell transplantation can ameliorate the phenotype of a mouse model of spinal muscular atrophyStefania Corti, Monica Nizzardo, Martina Nardini, et al.
Epilepsia Open|January 14, 2025
PAK3 pathogenic variant associated with sleep-related hypermotor epilepsy in a family with parental mosaicismAntonio Gambardella, Yu-Chi Liu, Mark F Bennett, et al.
Pageof 12

Showing results (71-80 of 120) with videos related to

Sort By:
Pageof 12
Journal of the Neurological Sciences|November 13, 2008
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunctionStefania Corti, Chiara Donadoni, Dario Ronchi, et al.
Annals of Clinical and Translational Neurology|April 25, 2020
Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiencyDario Ronchi, Edoardo Monfrini, Sara Bonato, et al.
BMC Neurology|July 14, 2011
Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G>A mitochondrial DNA mutation: a case reportDario Ronchi, Alessandra Cosi, Davide Tonduti, et al.
Human Mutation|August 16, 2005
Mutation finding in patients with dysferlin deficiency and role of the dysferlin interacting proteins annexin A1 and A2 in muscular dystrophiesRachele Cagliani, Francesca Magri, Antonio Toscano, et al.
Plos One|May 3, 2014
Mitochondrial changes in platelets are not related to those in skeletal muscle during human septic shockAlessandro Protti, Francesco Fortunato, Maria L Caspani, et al.
CNS Drugs|February 27, 2025
Exploring the Effectiveness of Adjunctive Cenobamate in Focal Epilepsy: A Time-Based AnalysisRoberta Roberti, Gianfranco Di Gennaro, Vittoria Cianci, et al.
Archives of Neurology|July 14, 2010
Mitochondrial respiratory chain dysfunction in muscle from patients with amyotrophic lateral sclerosisVeronica Crugnola, Costanza Lamperti, Valeria Lucchini, et al.
International Journal of Molecular Sciences|March 29, 2023
Extracellular Matrix Disorganization and Sarcolemmal Alterations in COL6-Related Myopathy Patients with New Variants of COL6 GenesSimona Zanotti, Francesca Magri, Sabrina Salani, et al.
The Journal of Clinical Investigation|September 5, 2008
Neural stem cell transplantation can ameliorate the phenotype of a mouse model of spinal muscular atrophyStefania Corti, Monica Nizzardo, Martina Nardini, et al.
Epilepsia Open|January 14, 2025
PAK3 pathogenic variant associated with sleep-related hypermotor epilepsy in a family with parental mosaicismAntonio Gambardella, Yu-Chi Liu, Mark F Bennett, et al.
Pageof 12