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Neuropediatrics|May 31, 2023
Early Muscle MRI Findings in a Pediatric Case of Emery-Dreifuss Muscular Dystrophy Type 1Chiara Panicucci, Sara Casalini, Monica Traverso, et al.
Journal of Human Genetics|March 21, 2018
Clinical and molecular consequences of exon 78 deletion in DMD geneMonica Traverso, Stefania Assereto, Serena Baratto, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|February 26, 2024
Skeletal muscle involvement in biallelic SORD mutations: case report and review of the literatureSara Massucco, Chiara Gemelli, Emilia Bellone, et al.
Stem Cell Research|January 6, 2018
Generation of human induced pluripotent stem cells (EURACi001-A, EURACi002-A, EURACi003-A) from peripheral blood mononuclear cells of three patients carrying mutations in the CAV3 geneViviana Meraviglia, Patrizia Benzoni, Sara Landi, et al.
International Journal of Molecular Sciences|January 23, 2024
Caveolin-3 and Caveolin-1 Interaction Decreases Channel Dysfunction Due to Caveolin-3 MutationsPatrizia Benzoni, Elisabetta Gazzerro, Chiara Fiorillo, et al.
Molecular Neurobiology|May 5, 2025
Exploratory Analysis of Gut Microbiota Profile in Duchenne Muscular Dystrophy (DMD) Patients with Intellectual DisabilityChiara Panicucci, Sara Casalini, Giovanni Fiorito, et al.
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.
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.
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