1) inflammatory myopathies
特发性肌炎
2) idiopathic inflammatory myopathies
特发性炎性肌病
1.
Research progress on functional exercises for patients with idiopathic inflammatory myopathies
特发性炎性肌病病人功能锻炼研究进展
2.
Idiopathic inflammatory myopathies (IIM) are a heterogeneous group of rare systemic connective tissue diseases.
特发性炎性肌病(IIM)的确切病因尚不清楚,近年来大量的资料提示遗传因素可能是重要的病因之一。
3.
Objective: To study the expression of major histocompatibility complex (MHC) on muscle biopsy specimens of idiopathic inflammatory myopathies(IIM) and analyze the composition and types of infiltrating monouclear cells, assess diagnostic value of MHC/T cell expression in IIM.
目的：研究MHC分子／T细胞在特发性炎性肌病(IIM)中的表达及在IIM诊断中的应用；研究凋亡相关分子和OX40分子在IIM中的表达及在IIM发病机制中可能起的作用。
3) Idiopathic inflammatory myopathy
特发性炎症性肌病
1.
Idiopathic inflammatory myopathy was misdiagnosed as dermatosis(6/16),lung diseases(5/16),abnormal hepatic function(2/16),rheumatic fever(2/16),and arrhythmia(1/16).
目的总结特发性炎症性肌病的临床表现,分析误诊原因,从而提高认识。
4) Polymyositis
[,pɔli,maiə'saitis]
多发性肌炎
1.
Dermatomyositis and Polymyositis Associated with Malignancy:A Retrospective Analysis of 21 Cases;
皮肌炎/多发性肌炎合并恶性肿瘤21例分析
2.
Clinical analysis of lung complications in polymyositis and dermatomyositis;
多发性肌炎/皮肌炎的肺部病变特点分析
3.
Chinese Medical Pattern Distribution of Polymyositis and Dermatomyositis;
多发性肌炎和皮肌炎中医证候分布规律探讨
5) myositis of indopathic orbital inflammatory pseudotumor
肌炎型特发性眼眶炎性假瘤
6) PM/DM
多发性肌炎/皮肌炎
1.
Analysis of misdiagnosis of 14 patients with polymyositis (PM/DM) complicated by interstitial lung disease;
14例多发性肌炎/皮肌炎的肺间质病变误诊分析
补充资料：家族性阵发性肌张力不全性舞蹈手足徐动症
家族性阵发性肌张力不全性舞蹈手足徐动症
familial paroxysmal myoclystonia choreoathetosis
系阵发性肌张力不全性舞蹈手足徐动症的一种类型。常染色体显性遗传，起病于婴儿期，有阵发性舞蹈手足徐动和肌张力不全运动，发作持续多在1小时以上，无意识障碍，脑电图正常。发病机制不明。用抗癫痫药物有效。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条