但是由于重症肌无力疾病本身的复杂性，疾病的个体差异和自然进展差异很大，因此术后一些病人的病情常有波动，在手术后无效、恶化、甚至死亡。
However, there were still some patients who showed no change or deteriorated and even died soon after surgery, for the complexity of MG in pathogenesis and the individual difference of patients.
目的观察血浆置换联合小剂量激素治疗重症肌无力的临床疗效及安全性。
Objective To explore the therapeutic effects of blood plasma replacement and small dose hormone on myasthenia gravis (MG).
方法对81例重症肌无力患者的死因进行回顾性分析。
Methods: To do retrospective analysis of death reasons in 81 MG patients.
目的研究重症肌无力(MG)患者临床绝对评分和电生理检查结果的相关性。
Objective To investigate the correlation between clinical absolute scores and electrophysiological parameters in patients with myasthenia gravis (MG).
重症肌无力（MG）是神经肌肉传递系统的自身免疫性疾病，常以眼症或全身性肌无力而发现。
Myasthenia gravis (MG) is an autoimmune disorder of neuromuscular transmission, usually recognized with ocular complaints or generalized muscle weakness.
结论TNF基因多态性与胸腺瘤发病及胸腺瘤发生重症肌无力相关。
Conclusion: TNF gene may be correlated with the susceptibility of thymoma and thymoma with MG.
目的探讨重症肌无力（MG）和癌性肌病（LEMS）时神经肌肉接头处（NMJ）的病理变化特点及其意义。
Objective The pathological changes on neuromuscular junction (NMJ) in the patients with myasthenia gravis (MG) or LambertEaton myasthenia syndrome (LEMS) were investigated comparatively.
目的：探讨喹诺酮类抗生素对重症肌无力(MG)治疗的安全性及其引起肌无力加重反应的可能机制。
Objective: To study the security of fluoroquinolone antibiotics and those underlying mechanisms of the exacerbation of myasthenia gravis (MG) following them.
目的探讨门诊长期使用醋酸泼尼松治疗重症肌无力(MG)的有效性、安全性和使用方法。
Objective the study was designed to evaluate the efficacy, safety, and applying method of long term prednisone therapy in treating the out patients with myasthenia gravis (MG).
目的：观察研究葡萄球菌蛋白A免疫吸附法治疗重症肌无力的近期疗效和安全性。
Objectives:To explore the clinical effect and safety of staphylococcal protein A immunoadsorption on myasthenia gravis patients.
方法回顾性分析1956 ~ 2004年诊治的218例患者369例次重症肌无力危象的病例资料。
Methods 369 clinical data of 218 patients with myasthenia gravis crisis between 1956 and 2004 were evaluated in a retrospective study.
方法回顾性分析了80例重症肌无力患者的发病年龄、发病诱因、临床表现、合并症及治疗效果。
Methods Retrospective analysis on age, clinical feature, treatment and affects were held on 80 patients with MG.
此型与暂时性新生儿重症肌无力不同，症状为持续性，无完全缓解。
This type of transient neonatal myasthenia gravis with different symptoms of persistent, non-complete remission.
此型与暂时性新生儿重症肌无力不同，症状为持续性，无完全缓解。
This type of transient neonatal myasthenia gravis with different symptoms of persistent, non-complete remission.
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