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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Spremljeno u:
Bibliografski detalji
Izdano u:Open Med (Wars)
Glavni autori: Murnyák, Balázs, Bodoki, Levente, Vincze, Melinda, Griger, Zoltán, Csonka, Tamás, Szepesi, Rita, Kurucz, Andrea, Dankó, Katalin, Hortobágyi, Tibor
Format: Artigo
Jezik:Inglês
Izdano: De Gruyter Open 2015
Teme:
Mini-Review
Online pristup: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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