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

Sonia Messina

Showing results (141-150 of 162) with videos related to

Pageof 17
Sort By:
Plos One|October 2, 2014
Long term natural history data in ambulant boys with Duchenne muscular dystrophy: 36-month changesMarika Pane, Elena Stacy Mazzone, Serena Sivo, et al.
Drugs in R&D|May 28, 2025
Opinion of the Italian Association of Myology on Ataluren for the Treatment of Nonsense Mutation Duchenne Muscular DystrophyLuca Bello, Pietro Riguzzi, Emilio Albamonte, et al.
Neurology|December 2, 2022
Prevalence of Spinal Muscular Atrophy in the Era of Disease-Modifying Therapies: An Italian Nationwide SurveyGiorgia Coratti, Martina Ricci, Anna Capasso, et al.
Plos Currents|February 3, 2015
The 6 minute walk test and performance of upper limb in ambulant duchenne muscular dystrophy boysMarika Pane, Elena Stacy Mazzone, Serena Sivo, et al.
Journal of Neuromuscular Diseases|April 17, 2023
Longitudinal Analysis of PUL 2.0 Domains in Ambulant and Non-Ambulant Duchenne Muscular Dystrophy Patients: How do they Change in Relation to Functional Ability?Marika Pane, Giorgia Coratti, Claudia Brogna, et al.
Annals of Clinical and Translational Neurology|March 19, 2026
Onasemnogene Abeparvovec in Type I Spinal Muscular Atrophy: 24-Month Follow-Up From the Italian RegistryMarika Pane, Giorgia Coratti, Chiara Cutrì, et al.
Genes|February 25, 2023
Using Cluster Analysis to Overcome the Limits of Traditional Phenotype-Genotype Correlations: The Example of <i>RYR1</i>-Related MyopathiesClaudia Dosi, Anna Rubegni, Jacopo Baldacci, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|February 16, 2023
Emergencies cards for neuromuscular disorders 1<sup>st</sup> Consensus Meeting from UILDM - Italian Muscular Dystrophy Association Workshop reportFabrizio Racca, Valeria A Sansone, Federica Ricci, et al.
Neuromuscular Disorders : NMD|December 29, 2023
Gain and loss of upper limb abilities in Duchenne muscular dystrophy patients: A 24-month studyGiorgia Coratti, Marika Pane, Claudia Brogna, et al.
European Journal of Pediatrics|December 16, 2024
Prevalence of Duchenne muscular dystrophy in Italy: a nationwide surveyAnna Capasso, Gianpaolo Cicala, Martina Ricci, et al.
Pageof 17

Showing results (141-150 of 162) with videos related to

Sort By:
Pageof 17
Plos One|October 2, 2014
Long term natural history data in ambulant boys with Duchenne muscular dystrophy: 36-month changesMarika Pane, Elena Stacy Mazzone, Serena Sivo, et al.
Drugs in R&D|May 28, 2025
Opinion of the Italian Association of Myology on Ataluren for the Treatment of Nonsense Mutation Duchenne Muscular DystrophyLuca Bello, Pietro Riguzzi, Emilio Albamonte, et al.
Neurology|December 2, 2022
Prevalence of Spinal Muscular Atrophy in the Era of Disease-Modifying Therapies: An Italian Nationwide SurveyGiorgia Coratti, Martina Ricci, Anna Capasso, et al.
Plos Currents|February 3, 2015
The 6 minute walk test and performance of upper limb in ambulant duchenne muscular dystrophy boysMarika Pane, Elena Stacy Mazzone, Serena Sivo, et al.
Journal of Neuromuscular Diseases|April 17, 2023
Longitudinal Analysis of PUL 2.0 Domains in Ambulant and Non-Ambulant Duchenne Muscular Dystrophy Patients: How do they Change in Relation to Functional Ability?Marika Pane, Giorgia Coratti, Claudia Brogna, et al.
Annals of Clinical and Translational Neurology|March 19, 2026
Onasemnogene Abeparvovec in Type I Spinal Muscular Atrophy: 24-Month Follow-Up From the Italian RegistryMarika Pane, Giorgia Coratti, Chiara Cutrì, et al.
Genes|February 25, 2023
Using Cluster Analysis to Overcome the Limits of Traditional Phenotype-Genotype Correlations: The Example of <i>RYR1</i>-Related MyopathiesClaudia Dosi, Anna Rubegni, Jacopo Baldacci, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|February 16, 2023
Emergencies cards for neuromuscular disorders 1<sup>st</sup> Consensus Meeting from UILDM - Italian Muscular Dystrophy Association Workshop reportFabrizio Racca, Valeria A Sansone, Federica Ricci, et al.
Neuromuscular Disorders : NMD|December 29, 2023
Gain and loss of upper limb abilities in Duchenne muscular dystrophy patients: A 24-month studyGiorgia Coratti, Marika Pane, Claudia Brogna, et al.
European Journal of Pediatrics|December 16, 2024
Prevalence of Duchenne muscular dystrophy in Italy: a nationwide surveyAnna Capasso, Gianpaolo Cicala, Martina Ricci, et al.
Pageof 17