Inclusion body myositis – pathomechanism and lessons from genetics

Inclusion body myositis is a rare, late-onset myopathy. Both inflammatory and myodegenerative features play an important role in their pathogenesis. Overlapping clinicopathological entities are the familial inclusion body myopathies with or without dementia. These myopathies share several clinical a...

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Detalles Bibliográficos
Autores principales: Murnyák, Balázs, Bodoki, Levente, Vincze, Melinda, Griger, Zoltán, Csonka, Tamás, Szepesi, Rita, Kurucz, Andrea, Dankó, Katalin, Hortobágyi, Tibor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter Open 2015
Materias:
Mini-Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5152972/
https://www.ncbi.nlm.nih.gov/pubmed/28352694
http://dx.doi.org/10.1515/med-2015-0030

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5152972/
https://www.ncbi.nlm.nih.gov/pubmed/28352694
http://dx.doi.org/10.1515/med-2015-0030

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