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Stefania Corti

Showing results (191-200 of 287) with videos related to

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Frontiers in Genetics|December 15, 2023
Prominent muscle involvement in a familial form of mitochondrial disease due to a <i>COA8</i> variantMartina Rimoldi, Francesca Magri, Sara Antognozzi, et al.
Frontiers in Neurology|March 19, 2024
Case report: A novel <i>ACTA1</i> variant in a patient with nemaline rods and increased glycogen depositionDaniela Piga, Martina Rimoldi, Francesca Magri, et al.
Frontiers in Psychology|May 1, 2015
Managing chronic pathologies with a stepped mHealth-based approach in clinical psychology and medicineGianluca Castelnuovo, Italo Zoppis, Eugenio Santoro, et al.
Annals of Clinical and Translational Neurology|April 25, 2020
Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiencyDario Ronchi, Edoardo Monfrini, Sara Bonato, et al.
Scientific Reports|April 14, 2022
Clinical and genetic features of a cohort of patients with MFN2-related neuropathyElena Abati, Arianna Manini, Daniele Velardo, et al.
Cells|July 6, 2023
Characterization of Skeletal Muscle Biopsy and Derived Myoblasts in a Patient Carrying Arg14del Mutation in <i>Phospholamban</i> GeneSimona Zanotti, Michela Ripolone, Laura Napoli, et al.
BMC Neurology|January 18, 2013
POLG1 mutations and stroke like episodes: a distinct clinical entity rather than an atypical MELAS syndromeAntonella Cheldi, Dario Ronchi, Andreina Bordoni, et al.
Journal of the Neurological Sciences|November 13, 2008
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunctionStefania Corti, Chiara Donadoni, Dario Ronchi, et al.
Ageing Research Reviews|November 16, 2023
Genomic and transcriptomic advances in amyotrophic lateral sclerosisMafalda Rizzuti, Luca Sali, Valentina Melzi, et al.
Brain Sciences|December 23, 2023
Lafora Disease: A Case Report and Evolving Treatment AdvancementsCarola Rita Ferrari Aggradi, Martina Rimoldi, Gloria Romagnoli, et al.
Pageof 29

Showing results (191-200 of 287) with videos related to

Sort By:
Pageof 29
Frontiers in Genetics|December 15, 2023
Prominent muscle involvement in a familial form of mitochondrial disease due to a <i>COA8</i> variantMartina Rimoldi, Francesca Magri, Sara Antognozzi, et al.
Frontiers in Neurology|March 19, 2024
Case report: A novel <i>ACTA1</i> variant in a patient with nemaline rods and increased glycogen depositionDaniela Piga, Martina Rimoldi, Francesca Magri, et al.
Frontiers in Psychology|May 1, 2015
Managing chronic pathologies with a stepped mHealth-based approach in clinical psychology and medicineGianluca Castelnuovo, Italo Zoppis, Eugenio Santoro, et al.
Annals of Clinical and Translational Neurology|April 25, 2020
Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiencyDario Ronchi, Edoardo Monfrini, Sara Bonato, et al.
Scientific Reports|April 14, 2022
Clinical and genetic features of a cohort of patients with MFN2-related neuropathyElena Abati, Arianna Manini, Daniele Velardo, et al.
Cells|July 6, 2023
Characterization of Skeletal Muscle Biopsy and Derived Myoblasts in a Patient Carrying Arg14del Mutation in <i>Phospholamban</i> GeneSimona Zanotti, Michela Ripolone, Laura Napoli, et al.
BMC Neurology|January 18, 2013
POLG1 mutations and stroke like episodes: a distinct clinical entity rather than an atypical MELAS syndromeAntonella Cheldi, Dario Ronchi, Andreina Bordoni, et al.
Journal of the Neurological Sciences|November 13, 2008
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunctionStefania Corti, Chiara Donadoni, Dario Ronchi, et al.
Ageing Research Reviews|November 16, 2023
Genomic and transcriptomic advances in amyotrophic lateral sclerosisMafalda Rizzuti, Luca Sali, Valentina Melzi, et al.
Brain Sciences|December 23, 2023
Lafora Disease: A Case Report and Evolving Treatment AdvancementsCarola Rita Ferrari Aggradi, Martina Rimoldi, Gloria Romagnoli, et al.
Pageof 29