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41 | SRT2104 improves muscle and cognitive outcomes and has the potential to enhance μDys gene therapy in Duchenne muscular dystrophy Laura Lociuro1, A. Arcari2, O. Gjana1, G. Scolari1, S.R. Casati1|2, S. Zecchini2, M. Giovarelli2, C. Perrotta2, C. De Palma1 | 1Department of Medical Biotechnology and Translational Medicine (BioMeTra), Università degli Studi di Milano, Segrate (MI), Italy; 2Department of Biomedical and Clinical Sciences "Luigi Sacco" (DIBIC), Università degli Studi di Milano, Italy.
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Do neurogenic and cancer-induced muscle atrophy follow common or divergent paths?
1188Downloads: 726HTML: 39 -
A revised model for mitochondrial dysfunction in Duchenne muscular dystrophy
2044Downloads: 893HTML: 14 -
Clinical guidelines for traumatic brain injuries in children and boys
2283Downloads: 1334HTML: 21