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Stefania Corti

Showing results (61-70 of 287) with videos related to

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Human Molecular Genetics|June 9, 2016
iPSC-derived LewisX+CXCR4+β1-integrin+ neural stem cells improve the amyotrophic lateral sclerosis phenotype by preserving motor neurons and muscle innervation in human and rodent modelsMonica Nizzardo, Monica Bucchia, Agnese Ramirez, et al.
Cell Transplantation|October 10, 2012
Direct reprogramming of adult somatic cells into other lineages: past evidence and future perspectivesMonica Nizzardo, Chiara Simone, Marianna Falcone, et al.
Frontiers in Neurology|June 19, 2024
Sleep and sleep-related breathing disorders in patients with spinal muscular atrophy: a changing perspective from novel treatments?Elena Abati, Eleonora Mauri, Martina Rimoldi, et al.
Progress in Neurobiology|August 6, 2011
ALS genetic modifiers that increase survival of SOD1 mice and are suitable for therapeutic developmentGiulietta Riboldi, Monica Nizzardo, Chiara Simone, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|February 28, 2025
Myotonic Dystrophy type 2 unmasked by physical activity resumption following COVID-19 lockdown: case discussion and review of the literatureSabrina Lucchiari, Francesca Magri, Martina Rimoldi, et al.
International Journal of Molecular Sciences|January 11, 2018
Investigation of New Morpholino Oligomers to Increase Survival Motor Neuron Protein Levels in Spinal Muscular AtrophyAgnese Ramirez, Sebastiano G Crisafulli, Mafalda Rizzuti, et al.
Neurology. Genetics|July 11, 2022
Expanding the Phenotypic Spectrum of Vocal Cord and Pharyngeal Weakness With Distal Myopathy due to the p.S85C MATR3 MutationArianna Manini, Daniele Velardo, Patrizia Ciscato, et al.
Frontiers in Psychology|June 25, 2014
Obesity and outpatient rehabilitation using mobile technologies: the potential mHealth approachGianluca Castelnuovo, Gian Mauro Manzoni, Giada Pietrabissa, et al.
Molecular Biology Reports|January 24, 2014
In vitro analysis of splice site mutations in the CLCN1 gene using the minigene assayGianna Ulzi, Valeria A Sansone, Francesca Magri, et al.
Neurology. Genetics|December 20, 2021
Homozygous <i>SOD1</i> Variation L144S Produces a Severe Form of Amyotrophic Lateral Sclerosis in an Iranian FamilyDelia Gagliardi, Minoo Ahmadinejad, Roberto Del Bo, et al.
Pageof 29

Showing results (61-70 of 287) with videos related to

Sort By:
Pageof 29
Human Molecular Genetics|June 9, 2016
iPSC-derived LewisX+CXCR4+β1-integrin+ neural stem cells improve the amyotrophic lateral sclerosis phenotype by preserving motor neurons and muscle innervation in human and rodent modelsMonica Nizzardo, Monica Bucchia, Agnese Ramirez, et al.
Cell Transplantation|October 10, 2012
Direct reprogramming of adult somatic cells into other lineages: past evidence and future perspectivesMonica Nizzardo, Chiara Simone, Marianna Falcone, et al.
Frontiers in Neurology|June 19, 2024
Sleep and sleep-related breathing disorders in patients with spinal muscular atrophy: a changing perspective from novel treatments?Elena Abati, Eleonora Mauri, Martina Rimoldi, et al.
Progress in Neurobiology|August 6, 2011
ALS genetic modifiers that increase survival of SOD1 mice and are suitable for therapeutic developmentGiulietta Riboldi, Monica Nizzardo, Chiara Simone, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|February 28, 2025
Myotonic Dystrophy type 2 unmasked by physical activity resumption following COVID-19 lockdown: case discussion and review of the literatureSabrina Lucchiari, Francesca Magri, Martina Rimoldi, et al.
International Journal of Molecular Sciences|January 11, 2018
Investigation of New Morpholino Oligomers to Increase Survival Motor Neuron Protein Levels in Spinal Muscular AtrophyAgnese Ramirez, Sebastiano G Crisafulli, Mafalda Rizzuti, et al.
Neurology. Genetics|July 11, 2022
Expanding the Phenotypic Spectrum of Vocal Cord and Pharyngeal Weakness With Distal Myopathy due to the p.S85C MATR3 MutationArianna Manini, Daniele Velardo, Patrizia Ciscato, et al.
Frontiers in Psychology|June 25, 2014
Obesity and outpatient rehabilitation using mobile technologies: the potential mHealth approachGianluca Castelnuovo, Gian Mauro Manzoni, Giada Pietrabissa, et al.
Molecular Biology Reports|January 24, 2014
In vitro analysis of splice site mutations in the CLCN1 gene using the minigene assayGianna Ulzi, Valeria A Sansone, Francesca Magri, et al.
Neurology. Genetics|December 20, 2021
Homozygous <i>SOD1</i> Variation L144S Produces a Severe Form of Amyotrophic Lateral Sclerosis in an Iranian FamilyDelia Gagliardi, Minoo Ahmadinejad, Roberto Del Bo, et al.
Pageof 29