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Stefania Corti

Showing results (211-220 of 287) with videos related to

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Molecular Genetics and Metabolism Reports|June 27, 2022
A novel <i>RRM2B</i> mutation associated with mitochondrial DNA depletion syndromeMonica Fumagalli, Dario Ronchi, Maria Francesca Bedeschi, et al.
Muscle & Nerve|July 23, 2021
Impact of COVID-19 on the quality of life of patients with neuromuscular disorders in the Lombardy area, ItalyDelia Gagliardi, Gianluca Costamagna, Elena Abati, et al.
Journal of Cachexia, Sarcopenia and Muscle|March 11, 2023
Longitudinal transcriptomic analysis of mouse sciatic nerve reveals pathways associated with age-related muscle pathologyNicole Comfort, Meethila Gade, Madeleine Strait, et al.
Neurobiology of Aging|November 23, 2006
Absence of angiogenic genes modification in Italian ALS patientsRoberto Del Bo, Marina Scarlato, Serena Ghezzi, et al.
The Lancet. Neurology|September 18, 2021
Onasemnogene abeparvovec gene therapy for symptomatic infantile-onset spinal muscular atrophy type 1 (STR1VE-EU): an open-label, single-arm, multicentre, phase 3 trialEugenio Mercuri, Francesco Muntoni, Giovanni Baranello, et al.
Biochemical and Biophysical Research Communications|August 9, 2011
Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T>C mutationDario Ronchi, Andreina Bordoni, Alessandra Cosi, et al.
Brain : a Journal of Neurology|January 17, 2019
Key role of SMN/SYNCRIP and RNA-Motif 7 in spinal muscular atrophy: RNA-Seq and motif analysis of human motor neuronsFederica Rizzo, Monica Nizzardo, Shikha Vashisht, et al.
Archives of Neurology|July 14, 2010
Mitochondrial respiratory chain dysfunction in muscle from patients with amyotrophic lateral sclerosisVeronica Crugnola, Costanza Lamperti, Valeria Lucchini, et al.
The Journal of Clinical Investigation|September 5, 2008
Neural stem cell transplantation can ameliorate the phenotype of a mouse model of spinal muscular atrophyStefania Corti, Monica Nizzardo, Martina Nardini, et al.
Annals of Clinical and Translational Neurology|April 11, 2024
Early spinal muscular atrophy treatment following newborn screening: A 20-month review of the first Italian regional experienceDelia Gagliardi, Eleonora Canzio, Paola Orsini, et al.
Pageof 29

Showing results (211-220 of 287) with videos related to

Sort By:
Pageof 29
Molecular Genetics and Metabolism Reports|June 27, 2022
A novel <i>RRM2B</i> mutation associated with mitochondrial DNA depletion syndromeMonica Fumagalli, Dario Ronchi, Maria Francesca Bedeschi, et al.
Muscle & Nerve|July 23, 2021
Impact of COVID-19 on the quality of life of patients with neuromuscular disorders in the Lombardy area, ItalyDelia Gagliardi, Gianluca Costamagna, Elena Abati, et al.
Journal of Cachexia, Sarcopenia and Muscle|March 11, 2023
Longitudinal transcriptomic analysis of mouse sciatic nerve reveals pathways associated with age-related muscle pathologyNicole Comfort, Meethila Gade, Madeleine Strait, et al.
Neurobiology of Aging|November 23, 2006
Absence of angiogenic genes modification in Italian ALS patientsRoberto Del Bo, Marina Scarlato, Serena Ghezzi, et al.
The Lancet. Neurology|September 18, 2021
Onasemnogene abeparvovec gene therapy for symptomatic infantile-onset spinal muscular atrophy type 1 (STR1VE-EU): an open-label, single-arm, multicentre, phase 3 trialEugenio Mercuri, Francesco Muntoni, Giovanni Baranello, et al.
Biochemical and Biophysical Research Communications|August 9, 2011
Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T>C mutationDario Ronchi, Andreina Bordoni, Alessandra Cosi, et al.
Brain : a Journal of Neurology|January 17, 2019
Key role of SMN/SYNCRIP and RNA-Motif 7 in spinal muscular atrophy: RNA-Seq and motif analysis of human motor neuronsFederica Rizzo, Monica Nizzardo, Shikha Vashisht, et al.
Archives of Neurology|July 14, 2010
Mitochondrial respiratory chain dysfunction in muscle from patients with amyotrophic lateral sclerosisVeronica Crugnola, Costanza Lamperti, Valeria Lucchini, et al.
The Journal of Clinical Investigation|September 5, 2008
Neural stem cell transplantation can ameliorate the phenotype of a mouse model of spinal muscular atrophyStefania Corti, Monica Nizzardo, Martina Nardini, et al.
Annals of Clinical and Translational Neurology|April 11, 2024
Early spinal muscular atrophy treatment following newborn screening: A 20-month review of the first Italian regional experienceDelia Gagliardi, Eleonora Canzio, Paola Orsini, et al.
Pageof 29