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Adele D'Amico

Showing results (1-10 of 246) with videos related to

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Current Neurology and Neuroscience Reports|March 28, 2008
Congenital myopathiesAdele D'Amico, Enrico Bertini
Endocrine Development|April 2, 2009
Mitochondrial encephalomyopathies and related syndromes: brief reviewEnrico Bertini, Adele D'Amico
Handbook of Clinical Neurology|April 30, 2013
Metabolic neuropathies and myopathiesAdele D'Amico, Enrico Bertini
Seminars in Pediatric Neurology|December 17, 2011
Congenital muscular dystrophies: a brief reviewEnrico Bertini, Adele D'Amico, Francesca Gualandi, et al.
Orphanet Journal of Rare Diseases|November 4, 2011
Spinal muscular atrophyAdele D'Amico, Eugenio Mercuri, Francesco D Tiziano, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 3, 2026
Fat embolism syndrome in Duchenne muscular dystrophy: an underdiagnosed complicationMichele Tosi, Michela Catteruccia, Nicoletta Cantarutti, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 9, 2022
Switching therapies: safety profile of Onasemnogene abeparvovec-xioi in a SMA1 patient previously treated with RisdiplamMichele Tosi, Michela Catteruccia, Claudio Cherchi, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|July 29, 2014
Effect of mexiletine on transitory depression of compound motor action potential in recessive myotonia congenitaMauro Lo Monaco, Adele D'Amico, Marco Luigetti, et al.
JCI Insight|August 8, 2025
STAC3 binding to CaV1.1 II-III loop is nonessential but critically supports skeletal muscle excitation-contraction couplingWietske E Tuinte, Enikő Török, Petronel Tuluc, et al.
EMBO Molecular Medicine|March 23, 2011
miRNAs as serum biomarkers for Duchenne muscular dystrophyDavide Cacchiarelli, Ivano Legnini, Julie Martone, et al.
Pageof 25

Showing results (1-10 of 246) with videos related to

Sort By:
Pageof 25
Current Neurology and Neuroscience Reports|March 28, 2008
Congenital myopathiesAdele D'Amico, Enrico Bertini
Endocrine Development|April 2, 2009
Mitochondrial encephalomyopathies and related syndromes: brief reviewEnrico Bertini, Adele D'Amico
Handbook of Clinical Neurology|April 30, 2013
Metabolic neuropathies and myopathiesAdele D'Amico, Enrico Bertini
Seminars in Pediatric Neurology|December 17, 2011
Congenital muscular dystrophies: a brief reviewEnrico Bertini, Adele D'Amico, Francesca Gualandi, et al.
Orphanet Journal of Rare Diseases|November 4, 2011
Spinal muscular atrophyAdele D'Amico, Eugenio Mercuri, Francesco D Tiziano, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 3, 2026
Fat embolism syndrome in Duchenne muscular dystrophy: an underdiagnosed complicationMichele Tosi, Michela Catteruccia, Nicoletta Cantarutti, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 9, 2022
Switching therapies: safety profile of Onasemnogene abeparvovec-xioi in a SMA1 patient previously treated with RisdiplamMichele Tosi, Michela Catteruccia, Claudio Cherchi, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|July 29, 2014
Effect of mexiletine on transitory depression of compound motor action potential in recessive myotonia congenitaMauro Lo Monaco, Adele D'Amico, Marco Luigetti, et al.
JCI Insight|August 8, 2025
STAC3 binding to CaV1.1 II-III loop is nonessential but critically supports skeletal muscle excitation-contraction couplingWietske E Tuinte, Enikő Török, Petronel Tuluc, et al.
EMBO Molecular Medicine|March 23, 2011
miRNAs as serum biomarkers for Duchenne muscular dystrophyDavide Cacchiarelli, Ivano Legnini, Julie Martone, et al.
Pageof 25