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

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 reliable bio...

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Detalles Bibliográficos
Autores principales: Ragozzino, Elvira, Bortolani, Sara, Di Pietro, Lorena, Papait, Andrea, Parolini, Ornella, Monforte, Mauro, Tasca, Giorgio, Ricci, Enzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10583430/
https://www.ncbi.nlm.nih.gov/pubmed/37849014
http://dx.doi.org/10.1186/s40478-023-01660-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10583430/
https://www.ncbi.nlm.nih.gov/pubmed/37849014
http://dx.doi.org/10.1186/s40478-023-01660-4

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