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Stefania Corti

Showing results (261-270 of 287) with videos related to

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Annals of Clinical and Translational Neurology|May 14, 2025
Myostatin Levels in SMA Following Disease-Modifying Treatments: A Multi-Center StudyFiorella Piemonte, Sara Petrillo, Anna Capasso, et al.
Nature Communications|November 5, 2020
Systematic elucidation of neuron-astrocyte interaction in models of amyotrophic lateral sclerosis using multi-modal integrated bioinformatics workflowVartika Mishra, Diane B Re, Virginia Le Verche, et al.
Neurology|May 9, 2014
Lower motor neuron disease with respiratory failure caused by a novel MAPT mutationAlessio Di Fonzo, Dario Ronchi, Francesca Gallia, et al.
European Journal of Human Genetics : EJHG|July 19, 2023
A biallelic variant in COX18 cause isolated Complex IV deficiency associated with neonatal encephalo-cardio-myopathy and axonal sensory neuropathyDario Ronchi, Manuela Garbellini, Francesca Magri, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|September 27, 2018
Mitochondrial dysfunction in fibroblasts of Multiple System AtrophyGiacomo Monzio Compagnoni, Giulio Kleiner, Andreina Bordoni, et al.
Stem Cell Reports|October 23, 2018
Mitochondrial Dysregulation and Impaired Autophagy in iPSC-Derived Dopaminergic Neurons of Multiple System AtrophyGiacomo Monzio Compagnoni, Giulio Kleiner, Maura Samarani, et al.
Neurobiology of Aging|July 7, 2012
C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effectAntonia Ratti, Lucia Corrado, Barbara Castellotti, et al.
Neurobiology of Aging|July 11, 2016
Mutational analysis of COQ2 in patients with MSA in ItalyDario Ronchi, Ernesto Di Biase, Giulia Franco, et al.
Neurobiology of Aging|October 16, 2012
Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementiaCinzia Tiloca, Nicola Ticozzi, Viviana Pensato, et al.
Eclinicalmedicine|May 17, 2023
Onasemnogene abeparvovec in spinal muscular atrophy: predictors of efficacy and safety in naïve patients with spinal muscular atrophy and following switch from other therapiesMarika Pane, Beatrice Berti, Anna Capasso, et al.
Pageof 29

Showing results (261-270 of 287) with videos related to

Sort By:
Pageof 29
Annals of Clinical and Translational Neurology|May 14, 2025
Myostatin Levels in SMA Following Disease-Modifying Treatments: A Multi-Center StudyFiorella Piemonte, Sara Petrillo, Anna Capasso, et al.
Nature Communications|November 5, 2020
Systematic elucidation of neuron-astrocyte interaction in models of amyotrophic lateral sclerosis using multi-modal integrated bioinformatics workflowVartika Mishra, Diane B Re, Virginia Le Verche, et al.
Neurology|May 9, 2014
Lower motor neuron disease with respiratory failure caused by a novel MAPT mutationAlessio Di Fonzo, Dario Ronchi, Francesca Gallia, et al.
European Journal of Human Genetics : EJHG|July 19, 2023
A biallelic variant in COX18 cause isolated Complex IV deficiency associated with neonatal encephalo-cardio-myopathy and axonal sensory neuropathyDario Ronchi, Manuela Garbellini, Francesca Magri, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|September 27, 2018
Mitochondrial dysfunction in fibroblasts of Multiple System AtrophyGiacomo Monzio Compagnoni, Giulio Kleiner, Andreina Bordoni, et al.
Stem Cell Reports|October 23, 2018
Mitochondrial Dysregulation and Impaired Autophagy in iPSC-Derived Dopaminergic Neurons of Multiple System AtrophyGiacomo Monzio Compagnoni, Giulio Kleiner, Maura Samarani, et al.
Neurobiology of Aging|July 7, 2012
C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effectAntonia Ratti, Lucia Corrado, Barbara Castellotti, et al.
Neurobiology of Aging|July 11, 2016
Mutational analysis of COQ2 in patients with MSA in ItalyDario Ronchi, Ernesto Di Biase, Giulia Franco, et al.
Neurobiology of Aging|October 16, 2012
Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementiaCinzia Tiloca, Nicola Ticozzi, Viviana Pensato, et al.
Eclinicalmedicine|May 17, 2023
Onasemnogene abeparvovec in spinal muscular atrophy: predictors of efficacy and safety in naïve patients with spinal muscular atrophy and following switch from other therapiesMarika Pane, Beatrice Berti, Anna Capasso, et al.
Pageof 29