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Updated: Aug 13, 2026

Vascular Occlusion Training for Inclusion Body Myositis: A Novel Therapeutic Approach
Published on: June 5, 2010
[Hereditary inclusion-body myopathy]
1Katedry Chorób Wewnetrznych i Reumatologii, Slaskiej Akademii Medycznej w Katowicach.
Abstract:
Hereditary inclusion-body myopathy (h-IBM) is a heterogeneous group of disorders characterized by progressive weakness of some skeletal muscles and pathological feature, intercellular rimmed vacuoles in the muscular filaments. h-IBM is not associated with inflammatory infiltrations and term myopathy is used as opposite to spontaneous inclusion-body myositis. h-IBM is classified into autosomal recessive and autosomal dominant subgroups.
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