Muscle fibrosis as a prognostic biomarker in facioscapulohumeral muscular dystrophy: a retrospective cohort study

Abstract Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant epigenetic disorder with highly variable muscle involvement and disease progression. Ongoing clinical trials, aimed at counteracting muscle degeneration and disease progression in FSHD patients, increase the need for rel...

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Detalhes bibliográficos

Principais autores:	Elvira Ragozzino, Sara Bortolani, Lorena Di Pietro, Andrea Papait, Ornella Parolini, Mauro Monforte, Giorgio Tasca, Enzo Ricci
Formato:	Artigo
Idioma:	Inglês
Publicado em:	BMC 2023-10-01
coleção:	Acta Neuropathologica Communications
Assuntos:	Muscle fibrosis Skeletal muscle Facioscapulohumeral muscular dystrophy Neuromuscular disease Biomarker Muscle magnetic resonance imaging
Acesso em linha:	https://doi.org/10.1186/s40478-023-01660-4
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