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Francesca Magri

Showing results (151-160 of 174) with videos related to

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Muscle & Nerve|May 18, 2016
The italian limb girdle muscular dystrophy registry: Relative frequency, clinical features, and differential diagnosisFrancesca Magri, Vincenzo Nigro, Corrado Angelini, et al.
Acta Neuropathologica Communications|April 16, 2022
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population studyAurora Fusto, Denise Cassandrini, Chiara Fiorillo, et al.
Plos One|June 25, 2021
North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow upGiorgia Coratti, Marika Pane, Claudia Brogna, et al.
Plos One|January 18, 2013
24 month longitudinal data in ambulant boys with Duchenne muscular dystrophyElena Stacy Mazzone, Marika Pane, Maria Pia Sormani, et al.
Journal of Neurology|May 11, 2015
Centronuclear myopathies: genotype-phenotype correlation and frequency of defined genetic forms in an Italian cohortFabiana Fattori, Lorenzo Maggi, Claudio Bruno, et al.
Neurology|June 30, 2012
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophyLuca Bello, Luisa Piva, Andrea Barp, et al.
Plos One|December 5, 2015
Correction: Long Term Natural History Data in Ambulant Boys with Duchenne Muscular Dystrophy: 36-Month ChangesMarika Pane, Elena Stacy Mazzone, Serena Sivo, et al.
Plos One|March 17, 2016
Timed Rise from Floor as a Predictor of Disease Progression in Duchenne Muscular Dystrophy: An Observational StudyElena S Mazzone, Giorgia Coratti, Maria Pia Sormani, et al.
Annals of Clinical and Translational Neurology|April 29, 2020
Genetic modifiers of respiratory function in Duchenne muscular dystrophyLuca Bello, Grazia D'Angelo, Matteo Villa, et al.
Annals of Internal Medicine|September 3, 2019
Cardiac and Neuromuscular Features of Patients With LMNA-Related CardiomyopathyGiovanni Peretto, Chiara Di Resta, Jacopo Perversi, et al.
Pageof 18

Showing results (151-160 of 174) with videos related to

Sort By:
Pageof 18
Muscle & Nerve|May 18, 2016
The italian limb girdle muscular dystrophy registry: Relative frequency, clinical features, and differential diagnosisFrancesca Magri, Vincenzo Nigro, Corrado Angelini, et al.
Acta Neuropathologica Communications|April 16, 2022
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population studyAurora Fusto, Denise Cassandrini, Chiara Fiorillo, et al.
Plos One|June 25, 2021
North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow upGiorgia Coratti, Marika Pane, Claudia Brogna, et al.
Plos One|January 18, 2013
24 month longitudinal data in ambulant boys with Duchenne muscular dystrophyElena Stacy Mazzone, Marika Pane, Maria Pia Sormani, et al.
Journal of Neurology|May 11, 2015
Centronuclear myopathies: genotype-phenotype correlation and frequency of defined genetic forms in an Italian cohortFabiana Fattori, Lorenzo Maggi, Claudio Bruno, et al.
Neurology|June 30, 2012
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophyLuca Bello, Luisa Piva, Andrea Barp, et al.
Plos One|December 5, 2015
Correction: Long Term Natural History Data in Ambulant Boys with Duchenne Muscular Dystrophy: 36-Month ChangesMarika Pane, Elena Stacy Mazzone, Serena Sivo, et al.
Plos One|March 17, 2016
Timed Rise from Floor as a Predictor of Disease Progression in Duchenne Muscular Dystrophy: An Observational StudyElena S Mazzone, Giorgia Coratti, Maria Pia Sormani, et al.
Annals of Clinical and Translational Neurology|April 29, 2020
Genetic modifiers of respiratory function in Duchenne muscular dystrophyLuca Bello, Grazia D'Angelo, Matteo Villa, et al.
Annals of Internal Medicine|September 3, 2019
Cardiac and Neuromuscular Features of Patients With LMNA-Related CardiomyopathyGiovanni Peretto, Chiara Di Resta, Jacopo Perversi, et al.
Pageof 18