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Familial inflammatory inclusion body myositis

Patients and methods: Clinical, biological, MRI, and histological data were analysed in two siblings with inflammatory IBM and compared with those of patients with sporadic and hereditary IBM. Results: Both patients had a clinical phenotype of sporadic IBM, which differs from hereditary myopathies b...

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Bibliografski detalji
Glavni autori: Ranque-Francois, B, Maisonobe, T, Dion, E, Piette, J, Chauveheid, M, Amoura, Z, Papo, T
Format: Artigo
Jezik:Inglês
Izdano: 2005
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1755454/
https://ncbi.nlm.nih.gov/pubmed/15769920
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/ard.2004.025494
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