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Sonia Messina

Showing results (91-100 of 162) with videos related to

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Nature Medicine|August 11, 2014
Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and miceNicolas Wein, Adeline Vulin, Maria S Falzarano, et al.
Neuromuscular Disorders : NMD|June 8, 2021
Age related treatment effect in type II Spinal Muscular Atrophy pediatric patients treated with nusinersenGiorgia Coratti, Marika Pane, Simona Lucibello, et al.
Journal of Neurology|November 9, 2013
"I have got something positive out of this situation": psychological benefits of caregiving in relatives of young people with muscular dystrophyLorenza Magliano, Melania Patalano, Alessandra Sagliocchi, et al.
Muscle & Nerve|October 5, 2016
Revised upper limb module for spinal muscular atrophy: Development of a new moduleElena S Mazzone, Anna Mayhew, Jacqueline Montes, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|August 8, 2017
Integrated care of muscular dystrophies in Italy. Part 2. Psychological treatments, social and welfare support, and financial costsLorenza Magliano, Marianna Scutifero, Melania Patalano, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 11, 2017
Integrated care of muscular dystrophies in Italy. Part 1. Pharmacological treatment and rehabilitative interventionsLuisa Politano, Marianna Scutifero, Melania Patalano, et al.
Muscle & Nerve|November 4, 2014
Burden, professional support, and social network in families of children and young adults with muscular dystrophiesLorenza Magliano, Melania Patalano, Alessandra Sagliocchi, et al.
Eclinicalmedicine|December 17, 2024
Type I spinal muscular atrophy and disease modifying treatments: a nationwide study in children born since 2016Maria Carmela Pera, Giorgia Coratti, Marika Pane, et al.
Plos One|July 29, 2022
Age, corticosteroid treatment and site of mutations affect motor functional changes in young boys with Duchenne Muscular DystrophyGiorgia Coratti, Jacopo Lenkowicz, Giulia Norcia, et al.
Neuromuscular Disorders : NMD|March 7, 2017
Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvementsAdele D'Amico, Michela Catteruccia, Giovanni Baranello, et al.
Pageof 17

Showing results (91-100 of 162) with videos related to

Sort By:
Pageof 17
Nature Medicine|August 11, 2014
Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and miceNicolas Wein, Adeline Vulin, Maria S Falzarano, et al.
Neuromuscular Disorders : NMD|June 8, 2021
Age related treatment effect in type II Spinal Muscular Atrophy pediatric patients treated with nusinersenGiorgia Coratti, Marika Pane, Simona Lucibello, et al.
Journal of Neurology|November 9, 2013
"I have got something positive out of this situation": psychological benefits of caregiving in relatives of young people with muscular dystrophyLorenza Magliano, Melania Patalano, Alessandra Sagliocchi, et al.
Muscle & Nerve|October 5, 2016
Revised upper limb module for spinal muscular atrophy: Development of a new moduleElena S Mazzone, Anna Mayhew, Jacqueline Montes, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|August 8, 2017
Integrated care of muscular dystrophies in Italy. Part 2. Psychological treatments, social and welfare support, and financial costsLorenza Magliano, Marianna Scutifero, Melania Patalano, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 11, 2017
Integrated care of muscular dystrophies in Italy. Part 1. Pharmacological treatment and rehabilitative interventionsLuisa Politano, Marianna Scutifero, Melania Patalano, et al.
Muscle & Nerve|November 4, 2014
Burden, professional support, and social network in families of children and young adults with muscular dystrophiesLorenza Magliano, Melania Patalano, Alessandra Sagliocchi, et al.
Eclinicalmedicine|December 17, 2024
Type I spinal muscular atrophy and disease modifying treatments: a nationwide study in children born since 2016Maria Carmela Pera, Giorgia Coratti, Marika Pane, et al.
Plos One|July 29, 2022
Age, corticosteroid treatment and site of mutations affect motor functional changes in young boys with Duchenne Muscular DystrophyGiorgia Coratti, Jacopo Lenkowicz, Giulia Norcia, et al.
Neuromuscular Disorders : NMD|March 7, 2017
Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvementsAdele D'Amico, Michela Catteruccia, Giovanni Baranello, et al.
Pageof 17