| 1. | Model making of polymyositis ' spleen defiecency syndrome
多发性肌炎脾虚证模型的制作 |
| 2. | Diagnosis and typing progress of dermatomyositis and polymyositis
皮肌炎和多发性肌炎的诊断与分型进展 |
| 3. | Analysis of 17 patients with interstitial lung disease in polymyositis
多发性肌炎合并间质性肺病17例分析 |
| 4. | Analysis of misdiagnosis of 14 patients with polymyositis complicated by interstitial lung disease
皮肌炎的肺间质病变误诊分析 |
| 5. | 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 |
| 6. | Death causes of 15 polymyositis and dermatomyositis patients with interstitial pneumonia
皮肌炎和多发性肌炎合并间质性肺炎死亡原因分析 |
| 7. | Several immune system cell types and processes have been recently identified in muscle in inclusion body myositis , dermatomyositis , and polymyositis
近来，包涵体肌炎、皮肌炎、多发性肌炎中几种免疫细胞类型和免疫反应过程被认定。 |
| 8. | Myeloid dendritic cells , which contribute to an immunologic synapse responsible for activation of the adaptive immune system , are abundant within muscle in inclusion body myositis and polymyositis
作用于免疫突触反应、活化适应性免疫应答的髓样树突状细胞在包涵体肌炎和多发性肌炎中大量存在。 |
| 9. | Polymyositis ( pm ) and dermatoyositis ( dm ) , devastating inflammatory muscle diseases , are associated with the myositis - specific anti - jo - 1 autoantibody , found in 25 - 40 % of such patients . anti - jo - 1 antibodies react with histidyl - trna synthetase
抗组氨酰? trna合成酶抗体，临床上又称抗jo - 1抗体，是诊断这类疾病的标志性抗体。 |
| 10. | Mixed connective tissue disease ( mctd ) was defined as a connective tissue disorder characterized by the presence of high titers of a distinct autoantibody in combination with clinical features commonly seen in systemic lupus erythematosus ( sle ) , scleroderma , and polymyositis ( referred to as overlap syndrome )
摘要混合性结缔组织疾病是一种结缔组织异常的疾病，合并有高价且明确的自体抗体，临床上常有类似全身性红斑性狼疮，硬皮症及多发性肌炎的表现。 |
