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Stefania Corti

Showing results (271-280 of 287) with videos related to

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Eclinicalmedicine|May 21, 2026
The phenotypic spectrum and genetic determinants of severe spinal muscular atrophy in individuals with a single <i>SMN2</i> copy: an international retrospective observational studyGianpaolo Cicala, Anna Capasso, Marianna Villa, et al.
Muscle & Nerve|May 18, 2016
The italian limb girdle muscular dystrophy registry: Relative frequency, clinical features, and differential diagnosisFrancesca Magri, Vincenzo Nigro, Corrado Angelini, et al.
Brain : a Journal of Neurology|November 21, 2024
Lewy pathology formation in patient-derived GBA1 Parkinson's disease midbrain organoidsEmanuele Frattini, Gaia Faustini, Gianluca Lopez, et al.
Frontiers in Psychology|May 6, 2016
Psychological Considerations in the Assessment and Treatment of Pain in Neurorehabilitation and Psychological Factors Predictive of Therapeutic Response: Evidence and Recommendations from the Italian Consensus Conference on Pain in NeurorehabilitationGianluca Castelnuovo, Emanuele M Giusti, Gian Mauro Manzoni, et al.
Frontiers in Psychology|March 1, 2016
Psychological Treatments and Psychotherapies in the Neurorehabilitation of Pain: Evidences and Recommendations from the Italian Consensus Conference on Pain in NeurorehabilitationGianluca Castelnuovo, Emanuele M Giusti, Gian Mauro Manzoni, et al.
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.
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.
Muscle & Nerve|August 3, 2024
Six-minute walk test as outcome measure of fatigability in adults with spinal muscular atrophy treated with nusinersenAlessandra Govoni, Giulia Ricci, Silvia Bonanno, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 11, 2022
Adults with spinal muscular atrophy: a large-scale natural history study shows gender effect on diseaseLorenzo Maggi, Luca Bello, Silvia Bonanno, et al.
Neurobiology of Aging|May 20, 2014
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival studyPerry T C van Doormaal, Nicola Ticozzi, Cinzia Gellera, et al.
Pageof 29

Showing results (271-280 of 287) with videos related to

Sort By:
Pageof 29
Eclinicalmedicine|May 21, 2026
The phenotypic spectrum and genetic determinants of severe spinal muscular atrophy in individuals with a single <i>SMN2</i> copy: an international retrospective observational studyGianpaolo Cicala, Anna Capasso, Marianna Villa, et al.
Muscle & Nerve|May 18, 2016
The italian limb girdle muscular dystrophy registry: Relative frequency, clinical features, and differential diagnosisFrancesca Magri, Vincenzo Nigro, Corrado Angelini, et al.
Brain : a Journal of Neurology|November 21, 2024
Lewy pathology formation in patient-derived GBA1 Parkinson's disease midbrain organoidsEmanuele Frattini, Gaia Faustini, Gianluca Lopez, et al.
Frontiers in Psychology|May 6, 2016
Psychological Considerations in the Assessment and Treatment of Pain in Neurorehabilitation and Psychological Factors Predictive of Therapeutic Response: Evidence and Recommendations from the Italian Consensus Conference on Pain in NeurorehabilitationGianluca Castelnuovo, Emanuele M Giusti, Gian Mauro Manzoni, et al.
Frontiers in Psychology|March 1, 2016
Psychological Treatments and Psychotherapies in the Neurorehabilitation of Pain: Evidences and Recommendations from the Italian Consensus Conference on Pain in NeurorehabilitationGianluca Castelnuovo, Emanuele M Giusti, Gian Mauro Manzoni, et al.
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.
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.
Muscle & Nerve|August 3, 2024
Six-minute walk test as outcome measure of fatigability in adults with spinal muscular atrophy treated with nusinersenAlessandra Govoni, Giulia Ricci, Silvia Bonanno, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 11, 2022
Adults with spinal muscular atrophy: a large-scale natural history study shows gender effect on diseaseLorenzo Maggi, Luca Bello, Silvia Bonanno, et al.
Neurobiology of Aging|May 20, 2014
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival studyPerry T C van Doormaal, Nicola Ticozzi, Cinzia Gellera, et al.
Pageof 29