inclusion body myositis

1. Objective To further discuss the diagnostic criteria for characterize of inclusion body myositis ( IBM).
   目的探讨包涵体肌炎的诊断标准。
2. Shared blood and muscle CD8~+ T-cell expansions in inclusion body myositis
   包涵体肌炎患者的血液和肌肉均有CD8~+T细胞扩增
3. Pathological and immunopathological changes of polymyositis and inclusion body myositis
   多发性肌炎及包涵体肌炎的病理和免疫病理变化
4. Inclusion Body Myositis: A Case Report and Literature Review
   包涵体肌炎1例报告并文献复习
5. Generally, they can be classified into three different subgroups: polymyositis, dermatomyositis and inclusion body myositis.
   一般来说，它们可分为三个不同的亚组：多发性肌炎，皮肌炎和包涵体肌炎。
6. The most prevalent subtypes are multiple polymyositis ( PM), dermatomyositis ( DM) and inclusion body myositis ( IBM). The adenosine is the signaling molecule of autocrine or paracrine pathway, and plays an important role in maintaining the internal environment stability.
   以多发性肌炎（PM）、皮肌炎（DM）和包涵体肌炎（IBM）3个亚型最为多见。腺苷是细胞自分泌或旁分泌途径中的信号分子，在维持内环境稳定方面起重要作用。

noun

1. myositis characterized by weakness of limb muscles (especially the thighs and wrists and fingers)