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Luca Bello

Showing results (71-80 of 144) with videos related to

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Human Molecular Genetics|July 17, 2014
Discovery of serum protein biomarkers in the mdx mouse model and cross-species comparison to Duchenne muscular dystrophy patientsYetrib Hathout, Ramya L Marathi, Sree Rayavarapu, et al.
Cell Reports|September 1, 2015
TNF-α-Induced microRNAs Control Dystrophin Expression in Becker Muscular DystrophyAlyson A Fiorillo, Christopher R Heier, James S Novak, et al.
Muscle & Nerve|September 29, 2011
Clinical and molecular characterization of limb-girdle muscular dystrophy due to LAMA2 mutationsBruno F Gavassini, Nicola Carboni, Jørgen E Nielsen, et al.
Cellular and Molecular Neurobiology|November 14, 2014
VBP15, a novel anti-inflammatory, is effective at reducing the severity of murine experimental autoimmune encephalomyelitisBlythe C Dillingham, Susan M Knoblach, Gina M Many, et al.
Journal of Neurology|January 3, 2022
Quality of life assessment in adult spinal muscular atrophy patients treated with nusinersenSilvia Bonanno, Riccardo Zanin, Luca Bello, 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|September 28, 2018
The clinical spectrum of <i>CASQ1</i>-related myopathyClaudio Semplicini, Cinzia Bertolin, Luca Bello, et al.
European Journal of Neurology|April 15, 2025
Robotic Thymectomy for Myasthenia Gravis: Analysis of the Surgical and Neurological Outcomes After a 20 Years' ExperienceGiovanni M Comacchio, Marco Schiavon, Luca Bello, et al.
Neurology. Genetics|June 8, 2026
Reducing Body Myopathy in Female Patients With <i>FHL1</i> Variants Showing Rapid and Severe Evolution Mimicking Inflammatory Myopathy: A Case SeriesGianmarco Severa, Christine Barnerias, Cyril Gitiaux, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 28, 2015
Non-neural phenotype of spinal and bulbar muscular atrophy: results from a large cohort of Italian patientsGiorgia Querin, Cinzia Bertolin, Elisa Da Re, et al.
Pageof 15

Showing results (71-80 of 144) with videos related to

Sort By:
Pageof 15
Human Molecular Genetics|July 17, 2014
Discovery of serum protein biomarkers in the mdx mouse model and cross-species comparison to Duchenne muscular dystrophy patientsYetrib Hathout, Ramya L Marathi, Sree Rayavarapu, et al.
Cell Reports|September 1, 2015
TNF-α-Induced microRNAs Control Dystrophin Expression in Becker Muscular DystrophyAlyson A Fiorillo, Christopher R Heier, James S Novak, et al.
Muscle & Nerve|September 29, 2011
Clinical and molecular characterization of limb-girdle muscular dystrophy due to LAMA2 mutationsBruno F Gavassini, Nicola Carboni, Jørgen E Nielsen, et al.
Cellular and Molecular Neurobiology|November 14, 2014
VBP15, a novel anti-inflammatory, is effective at reducing the severity of murine experimental autoimmune encephalomyelitisBlythe C Dillingham, Susan M Knoblach, Gina M Many, et al.
Journal of Neurology|January 3, 2022
Quality of life assessment in adult spinal muscular atrophy patients treated with nusinersenSilvia Bonanno, Riccardo Zanin, Luca Bello, 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|September 28, 2018
The clinical spectrum of <i>CASQ1</i>-related myopathyClaudio Semplicini, Cinzia Bertolin, Luca Bello, et al.
European Journal of Neurology|April 15, 2025
Robotic Thymectomy for Myasthenia Gravis: Analysis of the Surgical and Neurological Outcomes After a 20 Years' ExperienceGiovanni M Comacchio, Marco Schiavon, Luca Bello, et al.
Neurology. Genetics|June 8, 2026
Reducing Body Myopathy in Female Patients With <i>FHL1</i> Variants Showing Rapid and Severe Evolution Mimicking Inflammatory Myopathy: A Case SeriesGianmarco Severa, Christine Barnerias, Cyril Gitiaux, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 28, 2015
Non-neural phenotype of spinal and bulbar muscular atrophy: results from a large cohort of Italian patientsGiorgia Querin, Cinzia Bertolin, Elisa Da Re, et al.
Pageof 15