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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Guardat en:
Dades bibliogràfiques
Publicat a:Open Med (Wars)
Autors principals: Murnyák, Balázs, Bodoki, Levente, Vincze, Melinda, Griger, Zoltán, Csonka, Tamás, Szepesi, Rita, Kurucz, Andrea, Dankó, Katalin, Hortobágyi, Tibor
Format: Artigo
Idioma:Inglês
Publicat: De Gruyter Open 2015
Matèries:
Mini-Review
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5152972/
https://ncbi.nlm.nih.gov/pubmed/28352694
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1515/med-2015-0030
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