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Stefania Corti

Showing results (161-170 of 287) with videos related to

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BMC Neurology|April 24, 2023
Ischemic optic neuropathy as first presentation in patient with m.3243 A > G MELAS classic mutationSimone Scarcella, Laura Dell'Arti, Delia Gagliardi, et al.
Science Advances|November 25, 2015
Gene therapy rescues disease phenotype in a spinal muscular atrophy with respiratory distress type 1 (SMARD1) mouse modelMonica Nizzardo, Chiara Simone, Federica Rizzo, et al.
International Journal of Molecular Sciences|June 27, 2024
Association between <i>ZASP/LDB3</i> Pro26Ser and Inclusion Body MyopathyDaniela Piga, Simona Zanotti, Michela Ripolone, et al.
Scientific Reports|April 7, 2017
Genome-wide RNA-seq of iPSC-derived motor neurons indicates selective cytoskeletal perturbation in Brown-Vialetto disease that is partially rescued by riboflavinFederica Rizzo, Agnese Ramirez, Claudia Compagnucci, et al.
Frontiers in Neurology|September 24, 2021
Sodium Levels Predict Disability at Discharge in Guillain-Barré Syndrome: A Retrospective Cohort StudyDelia Gagliardi, Irene Faravelli, Manuel Alfredo Podestà, et al.
International Journal of Molecular Sciences|September 9, 2022
Antisense Morpholino-Based In Vitro Correction of a Pseudoexon-Generating Variant in the <i>SGCB</i> GeneFrancesca Magri, Simona Zanotti, Sabrina Salani, et al.
Frontiers in Neurology|August 18, 2018
Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect. A Case Report and a Review of the LiteratureDelia Gagliardi, Irene Faravelli, Luisa Villa, et al.
Frontiers in Genetics|June 15, 2026
Glycogenin-1 deficiency: a case report and review of the literatureNicola Molitierno, Daniele Velardo, Giulia Salvucci, et al.
Journal of Neurology|October 2, 2022
Correlation between clinical phenotype and electromyographic parameters in amyotrophic lateral sclerosisEleonora Colombo, Alberto Doretti, Francesco Scheveger, et al.
Glia|September 1, 2025
C9orf72 Repeat Expansion Induces Metabolic Dysfunction in Human iPSC-Derived Microglia and Modulates Glial-Neuronal CrosstalkMarika Mearelli, Insa Hirschberg, Christin Weissleder, et al.
Pageof 29

Showing results (161-170 of 287) with videos related to

Sort By:
Pageof 29
BMC Neurology|April 24, 2023
Ischemic optic neuropathy as first presentation in patient with m.3243 A > G MELAS classic mutationSimone Scarcella, Laura Dell'Arti, Delia Gagliardi, et al.
Science Advances|November 25, 2015
Gene therapy rescues disease phenotype in a spinal muscular atrophy with respiratory distress type 1 (SMARD1) mouse modelMonica Nizzardo, Chiara Simone, Federica Rizzo, et al.
International Journal of Molecular Sciences|June 27, 2024
Association between <i>ZASP/LDB3</i> Pro26Ser and Inclusion Body MyopathyDaniela Piga, Simona Zanotti, Michela Ripolone, et al.
Scientific Reports|April 7, 2017
Genome-wide RNA-seq of iPSC-derived motor neurons indicates selective cytoskeletal perturbation in Brown-Vialetto disease that is partially rescued by riboflavinFederica Rizzo, Agnese Ramirez, Claudia Compagnucci, et al.
Frontiers in Neurology|September 24, 2021
Sodium Levels Predict Disability at Discharge in Guillain-Barré Syndrome: A Retrospective Cohort StudyDelia Gagliardi, Irene Faravelli, Manuel Alfredo Podestà, et al.
International Journal of Molecular Sciences|September 9, 2022
Antisense Morpholino-Based In Vitro Correction of a Pseudoexon-Generating Variant in the <i>SGCB</i> GeneFrancesca Magri, Simona Zanotti, Sabrina Salani, et al.
Frontiers in Neurology|August 18, 2018
Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect. A Case Report and a Review of the LiteratureDelia Gagliardi, Irene Faravelli, Luisa Villa, et al.
Frontiers in Genetics|June 15, 2026
Glycogenin-1 deficiency: a case report and review of the literatureNicola Molitierno, Daniele Velardo, Giulia Salvucci, et al.
Journal of Neurology|October 2, 2022
Correlation between clinical phenotype and electromyographic parameters in amyotrophic lateral sclerosisEleonora Colombo, Alberto Doretti, Francesco Scheveger, et al.
Glia|September 1, 2025
C9orf72 Repeat Expansion Induces Metabolic Dysfunction in Human iPSC-Derived Microglia and Modulates Glial-Neuronal CrosstalkMarika Mearelli, Insa Hirschberg, Christin Weissleder, et al.
Pageof 29