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Chiara Fiorillo

Showing results (81-90 of 142) with videos related to

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Frontiers in Genetics|December 20, 2024
Case report: A single novel calpain 3 gene variant associated with mild myopathySara Massucco, Paola Fossa, Chiara Fiorillo, et al.
Acta Neuropathologica Communications|October 20, 2023
Myopathologic trajectory in Duchenne muscular dystrophy (DMD) reveals lack of regeneration due to senescence in satellite cellsNastasia Cardone, Valentina Taglietti, Serena Baratto, et al.
The American Journal of Pathology|November 19, 2018
The Danger Signal Extracellular ATP Is Involved in the Immunomediated Damage of α-Sarcoglycan-Deficient Muscular DystrophyElisabetta Gazzerro, Serena Baratto, Stefania Assereto, et al.
Neurogenetics|April 25, 2012
TRPV4 mutations in children with congenital distal spinal muscular atrophyChiara Fiorillo, Francesca Moro, Giacomo Brisca, et al.
Frontiers in Neurology|October 22, 2021
The Role of Muscle Biopsy in Diagnostic Process of Infant Hypotonia: From Clinical Classification to the Genetic OutcomeMarco Veneruso, Chiara Fiorillo, Paolo Broda, et al.
Neuromuscular Disorders : NMD|February 12, 2013
Centronuclear myopathy related to dynamin 2 mutations: clinical, morphological, muscle imaging and genetic features of an Italian cohortMichela Catteruccia, Fabiana Fattori, Valentina Codemo, et al.
Pediatric Neurology|March 1, 2024
Early Onset Inherited Peripheral Neuropathies: The Experience of a Specialized Referral Center for Genetic Diagnosis AchievementAlessandro Geroldi, Clarissa Ponti, Alessia Mammi, et al.
Journal of Neurology|May 16, 2017
Muscle MRI in neutral lipid storage disease (NLSD)Matteo Garibaldi, Giorgio Tasca, Jordi Diaz-Manera, et al.
Journal of Neurology|June 14, 2017
Erratum to: Muscle MRI in neutral lipid storage disease (NLSD)Matteo Garibaldi, Giorgio Tasca, Jordi Diaz-Manera, et al.
Neuromuscular Disorders : NMD|March 28, 2016
Novel findings associated with MTM1 suggest a higher number of female symptomatic carriersMarco Savarese, Olimpia Musumeci, Teresa Giugliano, et al.
Pageof 15

Showing results (81-90 of 142) with videos related to

Sort By:
Pageof 15
Frontiers in Genetics|December 20, 2024
Case report: A single novel calpain 3 gene variant associated with mild myopathySara Massucco, Paola Fossa, Chiara Fiorillo, et al.
Acta Neuropathologica Communications|October 20, 2023
Myopathologic trajectory in Duchenne muscular dystrophy (DMD) reveals lack of regeneration due to senescence in satellite cellsNastasia Cardone, Valentina Taglietti, Serena Baratto, et al.
The American Journal of Pathology|November 19, 2018
The Danger Signal Extracellular ATP Is Involved in the Immunomediated Damage of α-Sarcoglycan-Deficient Muscular DystrophyElisabetta Gazzerro, Serena Baratto, Stefania Assereto, et al.
Neurogenetics|April 25, 2012
TRPV4 mutations in children with congenital distal spinal muscular atrophyChiara Fiorillo, Francesca Moro, Giacomo Brisca, et al.
Frontiers in Neurology|October 22, 2021
The Role of Muscle Biopsy in Diagnostic Process of Infant Hypotonia: From Clinical Classification to the Genetic OutcomeMarco Veneruso, Chiara Fiorillo, Paolo Broda, et al.
Neuromuscular Disorders : NMD|February 12, 2013
Centronuclear myopathy related to dynamin 2 mutations: clinical, morphological, muscle imaging and genetic features of an Italian cohortMichela Catteruccia, Fabiana Fattori, Valentina Codemo, et al.
Pediatric Neurology|March 1, 2024
Early Onset Inherited Peripheral Neuropathies: The Experience of a Specialized Referral Center for Genetic Diagnosis AchievementAlessandro Geroldi, Clarissa Ponti, Alessia Mammi, et al.
Journal of Neurology|May 16, 2017
Muscle MRI in neutral lipid storage disease (NLSD)Matteo Garibaldi, Giorgio Tasca, Jordi Diaz-Manera, et al.
Journal of Neurology|June 14, 2017
Erratum to: Muscle MRI in neutral lipid storage disease (NLSD)Matteo Garibaldi, Giorgio Tasca, Jordi Diaz-Manera, et al.
Neuromuscular Disorders : NMD|March 28, 2016
Novel findings associated with MTM1 suggest a higher number of female symptomatic carriersMarco Savarese, Olimpia Musumeci, Teresa Giugliano, et al.
Pageof 15