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Francesca Magri

Showing results (131-140 of 174) with videos related to

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Frontiers in Neurology|February 16, 2023
Givinostat for Becker muscular dystrophy: A randomized, placebo-controlled, double-blind studyGiacomo P Comi, Erik H Niks, Krista Vandenborne, et al.
Journal of Cellular and Molecular Medicine|February 8, 2020
Nusinersen treatment and cerebrospinal fluid neurofilaments: An explorative study on Spinal Muscular Atrophy type 3 patientsIrene Faravelli, Megi Meneri, Domenica Saccomanno, et al.
Neuromuscular Disorders : NMD|August 28, 2016
Histological effects of givinostat in boys with Duchenne muscular dystrophyPaolo Bettica, Stefania Petrini, Valentina D'Oria, et al.
Journal of Molecular Neuroscience : MN|April 24, 2016
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian PatientsDaniela Piga, Francesca Magri, Dario Ronchi, et al.
Journal of Neurology|March 15, 2011
Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-upFrancesca Magri, Alessandra Govoni, Maria Grazia D'Angelo, et al.
Plos One|October 30, 2015
Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated CardiomyopathyAndrea Barp, Luca Bello, Luisa Politano, et al.
American Journal of Human Genetics|January 29, 2013
Mutations in DNA2 link progressive myopathy to mitochondrial DNA instabilityDario Ronchi, Alessio Di Fonzo, Weiqiang Lin, et al.
Plos One|August 1, 2019
Correction: Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53Claudia Brogna, Giorgia Coratt, Marika Pane, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 3, 2026
Cardiac surveillance in the era of Duvyzat: do we need to do more?Marika Pane, Anna Capasso, Chiara Arpaia, et al.
Acta Neuropathologica|May 11, 2021
Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusionsMridul Johari, Jaakko Sarparanta, Anna Vihola, et al.
Pageof 18

Showing results (131-140 of 174) with videos related to

Sort By:
Pageof 18
Frontiers in Neurology|February 16, 2023
Givinostat for Becker muscular dystrophy: A randomized, placebo-controlled, double-blind studyGiacomo P Comi, Erik H Niks, Krista Vandenborne, et al.
Journal of Cellular and Molecular Medicine|February 8, 2020
Nusinersen treatment and cerebrospinal fluid neurofilaments: An explorative study on Spinal Muscular Atrophy type 3 patientsIrene Faravelli, Megi Meneri, Domenica Saccomanno, et al.
Neuromuscular Disorders : NMD|August 28, 2016
Histological effects of givinostat in boys with Duchenne muscular dystrophyPaolo Bettica, Stefania Petrini, Valentina D'Oria, et al.
Journal of Molecular Neuroscience : MN|April 24, 2016
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian PatientsDaniela Piga, Francesca Magri, Dario Ronchi, et al.
Journal of Neurology|March 15, 2011
Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-upFrancesca Magri, Alessandra Govoni, Maria Grazia D'Angelo, et al.
Plos One|October 30, 2015
Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated CardiomyopathyAndrea Barp, Luca Bello, Luisa Politano, et al.
American Journal of Human Genetics|January 29, 2013
Mutations in DNA2 link progressive myopathy to mitochondrial DNA instabilityDario Ronchi, Alessio Di Fonzo, Weiqiang Lin, et al.
Plos One|August 1, 2019
Correction: Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53Claudia Brogna, Giorgia Coratt, Marika Pane, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 3, 2026
Cardiac surveillance in the era of Duvyzat: do we need to do more?Marika Pane, Anna Capasso, Chiara Arpaia, et al.
Acta Neuropathologica|May 11, 2021
Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusionsMridul Johari, Jaakko Sarparanta, Anna Vihola, et al.
Pageof 18