Inflammatory features in sporadic late‐onset nemaline myopathy are independent from monoclonal gammopathy

Sporadic late‐onset nemaline myopathy (SLONM) is a rare adult‐onset non‐hereditary disease with subacute proximal muscle and often axial muscle weakness, characterized by the presence of nemaline bodies in skeletal muscle biopsies. Considering its association with concurrent monoclonal gammopathy of...

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Detalles Bibliográficos
Autores principales: Tanboon, Jantima, Uruha, Akinori, Arahata, Yukie, Dittmayer, Carsten, Schweizer, Leonille, Goebel, Hans‐Hilmar, Nishino, Ichizo, Stenzel, Werner
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Mini‐symposium
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8412091/
https://www.ncbi.nlm.nih.gov/pubmed/34043258
http://dx.doi.org/10.1111/bpa.12962

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8412091/
https://www.ncbi.nlm.nih.gov/pubmed/34043258
http://dx.doi.org/10.1111/bpa.12962

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