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Neuromuscular Disorders : NMD|October 22, 2018
Small mutation screening in the DMD gene by whole exome sequencing of an argentine Duchenne/Becker muscular dystrophies cohortLeonela N Luce, Micaela Carcione, Chiara Mazzanti, et al.
Frontiers in Pharmacology|June 21, 2021
Theragnosis for Duchenne Muscular DystrophyLeonela Luce, Micaela Carcione, Chiara Mazzanti, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 14, 2024
Prognostic significance of ACTN3 genotype in Duchenne muscular dystrophy: Findings from an Argentine patient cohortLeonela Luce, Chiara Mazzanti, Micaela Carcione, et al.
Neurology. Genetics|October 6, 2025
Whole-Body Skeletal Muscle MRI Patterns in Female Dystrophinopathy CarriersAlejandra P Vigliano, Leonela Luce, José Manuel Pastor Rueda, et al.
Neurology. Genetics|January 26, 2026
Erratum: Whole-Body Skeletal Muscle MRI Patterns in Female Dystrophinopathy CarriersAlejandra P Vigliano, Leonela Luce, José Manuel Pastor Rueda, et al.
Neuromuscular Disorders : NMD|January 16, 2021
Analysis of complex structural variants in the DMD gene in one familyLeonela Luce, Martín M Abelleyro, Micaela Carcione, et al.
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