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Brain Pathology (Zurich, Switzerland)|December 28, 2024
Protective role of Angiogenin in muscle regeneration in amyotrophic lateral sclerosis: Diagnostic and therapeutic implicationsPaola Fabbrizio, Sharada Baindoor, Cassandra Margotta, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 23, 2013
Arginine butyrate: a therapeutic candidate for Duchenne muscular dystrophySara Vianello, Hua Yu, Vincent Voisin, et al.
Neurology|September 28, 2018
The clinical spectrum of <i>CASQ1</i>-related myopathyClaudio Semplicini, Cinzia Bertolin, Luca Bello, et al.
Acta Neuropathologica Communications|May 24, 2025
Evaluation of aggrephagy markers in myofibrillar myopathiesEliana Iannibelli, Alessandra Ruggieri, Antonello Maruotti, et al.
American Journal of Human Genetics|October 18, 2016
Association Study of Exon Variants in the NF-κB and TGFβ Pathways Identifies CD40 as a Modifier of Duchenne Muscular DystrophyLuca Bello, Kevin M Flanigan, Robert B Weiss, et al.
Plos One|October 30, 2015
Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated CardiomyopathyAndrea Barp, Luca Bello, Luisa Politano, et al.
Acta Neuropathologica Communications|July 13, 2025
Kv3 channel agonist ameliorates the phenotype of a mouse model of amyotrophic lateral sclerosisManuela Marabita, Caterina Marchioretti, Aishwarya Aravamudhan, et al.
Journal of Neurology|May 5, 2022
Genetic modifiers of upper limb function in Duchenne muscular dystrophyDaniele Sabbatini, Aurora Fusto, Sara Vianello, et al.
Journal of Neuromuscular Diseases|February 16, 2024
The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient CardiomyopathyLuca Bello, Daniele Sabbatini, Aurora Fusto, et al.
Annals of Clinical and Translational Neurology|April 29, 2020
Genetic modifiers of respiratory function in Duchenne muscular dystrophyLuca Bello, Grazia D'Angelo, Matteo Villa, et al.
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