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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Open Med (Wars)
Egile Nagusiak: Murnyák, Balázs, Bodoki, Levente, Vincze, Melinda, Griger, Zoltán, Csonka, Tamás, Szepesi, Rita, Kurucz, Andrea, Dankó, Katalin, Hortobágyi, Tibor
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: De Gruyter Open 2015
Gaiak:
Mini-Review
Sarrera elektronikoa: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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