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Neuromuscular Disorders : NMD|November 5, 2021
The DMD gene and therapeutic approaches to restore dystrophinFernanda Fortunato, Marianna Farnè, Alessandra FerliniThe Lancet. Neurology|November 26, 2003
Dystrophin and mutations: one gene, several proteins, multiple phenotypesFrancesco Muntoni, Silvia Torelli, Alessandra FerliniOrphanet Journal of Rare Diseases|October 4, 2023
Rare diseases' genetic newborn screening as the gateway to future genomic medicine: the Screen4Care EU-IMI projectAlessandra Ferlini, Edith Sky Gross, Nicolas Garnier, et al.Nucleic Acid Therapeutics|February 11, 2014
Nanoparticle delivery of antisense oligonucleotides and their application in the exon skipping strategy for Duchenne muscular dystrophyMaria Sofia Falzarano, Chiara Passarelli, Alessandra FerliniNpj Imaging|March 24, 2026
Correlative multimodal imaging for microscale spatial mapping of collagen-gene activity interactions in human tissuesRiccardo Scodellaro, Martina Mietto, Alessandra Ferlini, et al.Experimental Cell Research|January 7, 2014
Biomarkers in rare neuromuscular diseasesChiara Scotton, Chiara Passarelli, Marcella Neri, et al.Neuromuscular Disorders : NMD|February 24, 2005
Recurrent syncope as persistently isolated feature of transthyretin amyloidotic polyneuropathyGiuseppe Vita, Anna Mazzeo, Rita Di Leo, et al.Journal of Clinical Medicine|March 6, 2021
Innovative Therapeutic Approaches for Duchenne Muscular DystrophyFernanda Fortunato, Rachele Rossi, Maria Sofia Falzarano, et al.Molecules (Basel, Switzerland)|October 13, 2015
Duchenne Muscular Dystrophy: From Diagnosis to TherapyMaria Sofia Falzarano, Chiara Scotton, Chiara Passarelli, et al.Biochemical 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.Pageof 26