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Sonia Messina

Showing results (61-70 of 162) with videos related to

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Plos One|March 24, 2020
Diagnostic journey in Spinal Muscular Atrophy: Is it still an odyssey?Maria Carmela Pera, Giorgia Coratti, Beatrice Berti, et al.
Cellular and Molecular Life Sciences : CMLS|September 10, 2024
Proteomics profiling and machine learning in nusinersen-treated patients with spinal muscular atrophyChiara Panicucci, Eray Sahin, Martina Bartolucci, et al.
Children (Basel, Switzerland)|June 26, 2026
Oral and Swallowing Abilities Tool (OrSAT) in Individuals with Type I SMA Older than 24 Months: A Pilot StudyGiulia Stanca, Maria Sframeli, Camilla Verdilio, et al.
Annals of Clinical and Translational Neurology|April 17, 2026
Safety and Tolerability of Givinostat: Evidence From Real-World and Clinical PracticeMarika Pane, Anna Capasso, Chiara Arpaia, et al.
Neurology|June 27, 2025
Spinal Muscular Atrophy Functional Composite Score Revised (SMA-FCR) in Untreated and Nusinersen-Treated Patient CohortsAmy Pasternak, Michael P McDermott, Jacqueline Montes, et al.
Annals of Neurology|October 31, 2012
DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsyRita Barone, Chiara Aiello, Valérie Race, et al.
Plos One|August 6, 2016
Revised North Star Ambulatory Assessment for Young Boys with Duchenne Muscular DystrophyEugenio Mercuri, Giorgia Coratti, Sonia Messina, et al.
Neuromuscular Disorders : NMD|August 28, 2016
Histological effects of givinostat in boys with Duchenne muscular dystrophyPaolo Bettica, Stefania Petrini, Valentina D'Oria, et al.
Journal of Molecular Neuroscience : MN|April 24, 2016
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian PatientsDaniela Piga, Francesca Magri, Dario Ronchi, et al.
Neuromuscular Disorders : NMD|September 9, 2020
Age and baseline values predict 12 and 24-month functional changes in type 2 SMAGiorgia Coratti, Maria C Pera, Simona Lucibello, et al.
Pageof 17

Showing results (61-70 of 162) with videos related to

Sort By:
Pageof 17
Plos One|March 24, 2020
Diagnostic journey in Spinal Muscular Atrophy: Is it still an odyssey?Maria Carmela Pera, Giorgia Coratti, Beatrice Berti, et al.
Cellular and Molecular Life Sciences : CMLS|September 10, 2024
Proteomics profiling and machine learning in nusinersen-treated patients with spinal muscular atrophyChiara Panicucci, Eray Sahin, Martina Bartolucci, et al.
Children (Basel, Switzerland)|June 26, 2026
Oral and Swallowing Abilities Tool (OrSAT) in Individuals with Type I SMA Older than 24 Months: A Pilot StudyGiulia Stanca, Maria Sframeli, Camilla Verdilio, et al.
Annals of Clinical and Translational Neurology|April 17, 2026
Safety and Tolerability of Givinostat: Evidence From Real-World and Clinical PracticeMarika Pane, Anna Capasso, Chiara Arpaia, et al.
Neurology|June 27, 2025
Spinal Muscular Atrophy Functional Composite Score Revised (SMA-FCR) in Untreated and Nusinersen-Treated Patient CohortsAmy Pasternak, Michael P McDermott, Jacqueline Montes, et al.
Annals of Neurology|October 31, 2012
DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsyRita Barone, Chiara Aiello, Valérie Race, et al.
Plos One|August 6, 2016
Revised North Star Ambulatory Assessment for Young Boys with Duchenne Muscular DystrophyEugenio Mercuri, Giorgia Coratti, Sonia Messina, et al.
Neuromuscular Disorders : NMD|August 28, 2016
Histological effects of givinostat in boys with Duchenne muscular dystrophyPaolo Bettica, Stefania Petrini, Valentina D'Oria, et al.
Journal of Molecular Neuroscience : MN|April 24, 2016
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian PatientsDaniela Piga, Francesca Magri, Dario Ronchi, et al.
Neuromuscular Disorders : NMD|September 9, 2020
Age and baseline values predict 12 and 24-month functional changes in type 2 SMAGiorgia Coratti, Maria C Pera, Simona Lucibello, et al.
Pageof 17