1) transient aggravation of muscle weakness
一过性肌无力加重
1.
Objective To study the effects of the transient aggravation of muscle weakness in methylprednisolone pulse therapy (MPPT) on myasthenia gravis (MG).
目的 观察甲基强的松龙冲击疗法 (MPPT)治疗重症肌无力 (MG)早期导致一过性肌无力加重的作用。
2) Myasthenia gravis
重症肌无力
1.
Preliminary experience on video assisted thoracic surgery(VATS) for thymoma and myasthenia gravis;
电视胸腔镜治疗胸腺瘤和重症肌无力
2.
Expression of single chain variable fragment A7 gene in myasthenia gravis in Pichia pastoris;
重症肌无力单链抗体A7基因在毕赤酵母中的表达
3.
Application of clinical absolute and relative score system in diagnosis for myasthenia gravis;
重症肌无力临床绝对和相对评分法在诊断中的应用
3) MG
重症肌无力
1.
Analysis of the clinical features of myasthenia gravis (MG) combined with Lambert-Eaton myasthenic syndrome (LEMS);
重症肌无力伴Lambert-Eaton肌无力综合征8例分析
2.
Comparison About the Diagnosing Value of Neostigmine Test and Repeatedly Low-frequency Stimulation in Diagnosing MG;
新斯的明试验与重复低频刺激对重症肌无力诊断意义的比较
3.
Objective: To explore the electropysiological features of patients with hyperthyroidism and myasthenia gravis (MG), and the relationship between it and chronic thyrotxic myopathy (CTM).
目的：探讨甲状腺机能亢进(甲亢)伴发重症肌无力(MG)患者的电生理检测特点,和与慢性甲状腺机能亢进性肌病(CTM)的关系。
4) myasthenia gravis (MG)
重症肌无力
1.
To observed the change of resiratory tract of 40 patients with myasthenia gravis (MG) during the therapy of thymus tissue resection or thymoma resection in this paper.
对40例重症肌无力病人切除胸腺组织或胸腺瘤治疗过程的围手术期呼吸道管理。
2.
Background and Objective Myasthenia gravis (MG) is one of autoimmune diseases caused by acetylcholine receptor antibodies (AchRAb), whose targets are the acetylcholine receptors (AchR) on the postsynaptic membrane at the neuromuscular junction (NMJ).
背景及目的 重症肌无力(myasthenia gravis，MG)主要是由乙酰胆碱受体抗体(acetylcholine receptor antibody，AchRAb)介导的，针对神经肌肉接头处突触后膜上乙酰胆碱受体(acetylcholine receptor，AchR)的自身免疫性疾病(AID)。
5) refractory myasthenia gravis
难治性重症肌无力
1.
Clinical study of double filtration plasmapheresis for treatment of refractory myasthenia gravis;
双重滤过血浆置换治疗难治性重症肌无力的临床研究
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