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Sonia Messina

Showing results (131-140 of 162) with videos related to

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Annals of Neurology|September 11, 2023
Clinical Phenotype of Pediatric and Adult Patients With Spinal Muscular Atrophy With Four SMN2 Copies: Are They Really All Stable?Martina Ricci, Gianpaolo Cicala, Anna Capasso, et al.
Plos One|June 21, 2018
Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal dataMarika Pane, Giorgia Coratti, Claudia Brogna, et al.
Journal of Neuromuscular Diseases|February 16, 2024
The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient CardiomyopathyLuca Bello, Daniele Sabbatini, Aurora Fusto, et al.
Neurology|June 30, 2012
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophyLuca Bello, Luisa Piva, Andrea Barp, et al.
Plos One|March 17, 2016
Timed Rise from Floor as a Predictor of Disease Progression in Duchenne Muscular Dystrophy: An Observational StudyElena S Mazzone, Giorgia Coratti, Maria Pia Sormani, et al.
Journal of Cell Science|March 6, 2016
Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathyChiara Scotton, Matteo Bovolenta, Elena Schwartz, et al.
Annals of Clinical and Translational Neurology|April 29, 2020
Genetic modifiers of respiratory function in Duchenne muscular dystrophyLuca Bello, Grazia D'Angelo, Matteo Villa, et al.
European Journal of Neurology|October 11, 2024
Long-term natural history in type II and III spinal muscular atrophy: a 4-year international study on the Hammersmith Functional Motor Scale ExpandedGiorgia Coratti, Francesca Bovis, Maria Carmela Pera, et al.
American Journal of Human Genetics|June 18, 2013
Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycanKeren J Carss, Elizabeth Stevens, A Reghan Foley, et al.
Neuromuscular Disorders : NMD|January 21, 2014
Reliability of the Performance of Upper Limb assessment in Duchenne muscular dystrophyMarika Pane, Elena S Mazzone, Lavinia Fanelli, et al.
Pageof 17

Showing results (131-140 of 162) with videos related to

Sort By:
Pageof 17
Annals of Neurology|September 11, 2023
Clinical Phenotype of Pediatric and Adult Patients With Spinal Muscular Atrophy With Four SMN2 Copies: Are They Really All Stable?Martina Ricci, Gianpaolo Cicala, Anna Capasso, et al.
Plos One|June 21, 2018
Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal dataMarika Pane, Giorgia Coratti, Claudia Brogna, et al.
Journal of Neuromuscular Diseases|February 16, 2024
The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient CardiomyopathyLuca Bello, Daniele Sabbatini, Aurora Fusto, et al.
Neurology|June 30, 2012
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophyLuca Bello, Luisa Piva, Andrea Barp, et al.
Plos One|March 17, 2016
Timed Rise from Floor as a Predictor of Disease Progression in Duchenne Muscular Dystrophy: An Observational StudyElena S Mazzone, Giorgia Coratti, Maria Pia Sormani, et al.
Journal of Cell Science|March 6, 2016
Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathyChiara Scotton, Matteo Bovolenta, Elena Schwartz, et al.
Annals of Clinical and Translational Neurology|April 29, 2020
Genetic modifiers of respiratory function in Duchenne muscular dystrophyLuca Bello, Grazia D'Angelo, Matteo Villa, et al.
European Journal of Neurology|October 11, 2024
Long-term natural history in type II and III spinal muscular atrophy: a 4-year international study on the Hammersmith Functional Motor Scale ExpandedGiorgia Coratti, Francesca Bovis, Maria Carmela Pera, et al.
American Journal of Human Genetics|June 18, 2013
Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycanKeren J Carss, Elizabeth Stevens, A Reghan Foley, et al.
Neuromuscular Disorders : NMD|January 21, 2014
Reliability of the Performance of Upper Limb assessment in Duchenne muscular dystrophyMarika Pane, Elena S Mazzone, Lavinia Fanelli, et al.
Pageof 17