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Biodrugs : Clinical Immunotherapeutics, Biopharmaceuticals and Gene Therapy|July 14, 2010
Stem cell therapies to treat muscular dystrophy: progress to dateMirella Meregalli, Andrea Farini, Daniele Parolini, et al.
Journal of Cellular Physiology|August 19, 2009
Cell based therapy for Duchenne muscular dystrophyAndrea Farini, Paola Razini, Silvia Erratico, et al.
Current Pharmaceutical Biotechnology|May 3, 2015
Drug delivery technologies and stem cells for tissue repair and regenerationGorka Orive, Raquel Cobos, Janire Gorriti, et al.
Tissue Engineering. Part B, Reviews|September 18, 2010
In vivo tracking of stem cell by nanotechnologies: future prospects for mouse to human translationChiara Villa, Silvia Erratico, Paola Razini, et al.
The FEBS Journal|December 5, 2012
Perspectives of stem cell therapy in Duchenne muscular dystrophyMirella Meregalli, Andrea Farini, Marzia Belicchi, et al.
Frontiers in Neurology|August 10, 2019
Preliminary Evidences of Safety and Efficacy of Flavonoids- and Omega 3-Based Compound for Muscular Dystrophies Treatment: A Randomized Double-Blind Placebo Controlled Pilot Clinical TrialClementina Sitzia, Mirella Meregalli, Marzia Belicchi, et al.
The American Journal of Pathology|August 1, 2009
Expression of parathyroid-specific genes in vascular endothelial progenitors of normal and tumoral parathyroid glandsSabrina Corbetta, Marzia Belicchi, Federica Pisati, et al.
Development (Cambridge, England)|February 18, 2016
Inositol 1,4,5-trisphosphate (IP3)-dependent Ca2+ signaling mediates delayed myogenesis in Duchenne muscular dystrophy fetal muscleAndrea Farini, Clementina Sitzia, Letizia Cassinelli, et al.
Cell Stem Cell|March 29, 2008
Restoration of human dystrophin following transplantation of exon-skipping-engineered DMD patient stem cells into dystrophic miceRachid Benchaouir, Mirella Meregalli, Andrea Farini, et al.
Human Molecular Genetics|July 2, 2017
Autologous intramuscular transplantation of engineered satellite cells induces exosome-mediated systemic expression of Fukutin-related protein and rescues disease phenotype in a murine model of limb-girdle muscular dystrophy type 2IPaola Frattini, Chiara Villa, Francesca De Santis, et al.
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