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Disease Models & Mechanisms|December 26, 2019
Cored in the act: the use of models to understand core myopathiesAurora Fusto, Louise A Moyle, Penney M Gilbert, et al.Acta Neuropathologica|May 13, 2018
Collagen VI is required for the structural and functional integrity of the neuromuscular junctionMatilde Cescon, Ilaria Gregorio, Nane Eiber, et al.Human Molecular Genetics|June 9, 2017
SPP1 genotype and glucocorticoid treatment modify osteopontin expression in Duchenne muscular dystrophy cellsSara Vianello, Boris Pantic, Aurora Fusto, et al.Biomolecules|November 27, 2025
<i>RYR1</i>-Related Myopathies Involve More than Calcium Dysregulation: Insights from Transcriptomic ProfilingDaniele Sabbatini, Domenico Gorgoglione, Giovanni Minervini, et al.Journal of Neurology|March 4, 2025
Deep characterization of females with heterozygous Duchenne muscular dystrophy mutationsPietro Riguzzi, Daniele Sabbatini, Aurora Fusto, et al.Acta Biomaterialia|May 28, 2021
De novo revertant fiber formation and therapy testing in a 3D culture model of Duchenne muscular dystrophy skeletal muscleMajid Ebrahimi, Heta Lad, Aurora Fusto, 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.Journal of Neurology|May 5, 2022
Genetic modifiers of upper limb function in Duchenne muscular dystrophyDaniele Sabbatini, Aurora Fusto, Sara Vianello, et al.Journal of Neuromuscular Diseases|February 16, 2024
The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient CardiomyopathyLuca Bello, Daniele Sabbatini, Aurora Fusto, 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.Pageof 1