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The Lancet. Neurology|November 26, 2003
Dystrophin and mutations: one gene, several proteins, multiple phenotypesFrancesco Muntoni, Silvia Torelli, Alessandra FerliniNeurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|November 21, 2008
Muscular dystrophies due to glycosylation defectsFrancesco Muntoni, Silvia Torelli, Martin BrockingtonBiochemical and Biophysical Research Communications|April 20, 2004
In vivo study of an aberrant dystrophin exon inclusion in X-linked dilated cardiomyopathyNiaz Cohen, Paola Rimessi, Francesca Gualandi, et al.Current Opinion in Neurology|March 17, 2004
Defective glycosylation in congenital muscular dystrophiesFrancesco Muntoni, Martin Brockington, Silvia Torelli, et al.Neuromuscular Disorders : NMD|September 11, 2007
Dystrophin levels as low as 30% are sufficient to avoid muscular dystrophy in the humanMarcella Neri, Silvia Torelli, Sue Brown, et al.Molecules (Basel, Switzerland)|April 6, 2017
Antisense Oligonucleotide-Based Therapy for Neuromuscular DiseaseValentina Sardone, Haiyan Zhou, Francesco Muntoni, et al.Current Opinion in Neurology|August 10, 2011
Muscular dystrophies due to glycosylation defects: diagnosis and therapeutic strategiesFrancesco Muntoni, Silvia Torelli, Dominic J Wells, et al.Lancet (London, England)|November 9, 2002
Defective glycosylation in muscular dystrophyFrancesco Muntoni, Martin Brockington, Derek J Blake, et al.Skeletal Muscle|November 29, 2024
Golodirsen restores DMD transcript imbalance in Duchenne Muscular Dystrophy patient muscle cellsRachele Rossi, Silvia Torelli, Marc Moore, et al.Frontiers in Physiology|June 2, 2023
MyoD-induced reprogramming of human fibroblasts and urinary stem cells <i>in vitro</i>: protocols and their applicationsRachele Rossi, Silvia Torelli, Pierpaolo Ala, et al.Pageof 77