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Objective To evaluate the long-term outcome of thymectomy combined with corticosteroid therapy for myasthenia gravis with thymoma.

目的 评价胸腺切除术并皮质类固醇疗法对伴胸腺瘤的重症肌无力患者的远期疗效。

Drug treatment and thymoma excision were effective approaches for MG.

药物治疗和胸腺切除术均为治疗重症肌无力的有效手段。

Methods CAE-Abs were evaluated by western blot assay in 33 patients with MG(16 cases with and 17 cases without thymoma),normal adults for 10 cases and 18 cases of other diseases.

采用免疫印迹法检测33例重症肌无力患者(有瘤16例及无瘤17例),正常人10名和其它疾病18例的血清中CAE抗体。

Parasitizing specially in the cytoplasma of small granular hemocytes, RLOs formed an inclusion body in host cell, in which, RLOs propagated in mass and caused the host cell swelling and disorganizing, subsequently released and infected other target histocytes, resulted in the arising of such symptoms as debility and shivering of limbs, etc..

RLOs专一性寄生于小颗粒细胞的胞质内,以包涵体的形式生长繁殖,随着RLOs的快速增殖,包涵体内RLOs数目显著增多,且多呈圆形,包涵体极度膨胀,将细胞核压向周边,最终细胞被胀破,释放出RLOs再去侵染其它组织和器官,造成颤抖、肌无力等全身症状。

The myasthenia survival condition also is striking Zhu Changqing innermost feelings, when she viewed that some children due to be taunted by the schoolmate for "curls upwards the foot" to leave school, henceforth to keep silent; more people painfully flinch in the area of study and employment. Then she made a silent decision in her heart: She cannot only consider about herself, must handle some matters for this community which including her.

肌无力者的生存状况也敲打着朱常青的内心,当看到有的孩子因为被同学嘲讽为&翘脚&哭着退学、从此不言不语,更多的人在读书、就业的一关关前痛苦地退缩,她心中默默地下了决心:不能独善其身,要为自己所属的这个群体做些事情。

Electron microscopic observation demonstrated excessive accumulation of lipid droplets and with abnormal mitochondria in some cases. Conclusions LSM was a complex disease. It was considered to be a subgroup of mitochondrial myopathies. Fatigue and muscle weakness were the prominent symptoms with recurring courses in most cases.

脂质沉积性肌病是一组生化方面十分复杂的疾病,属于线粒体肌病的一个类型,临床上以不能耐受运动和近端肌无力为主,病程呈波动性,部分可有自发缓解,肌肉病理检查有助于确诊。

Objective To investigate and verify the regulatory effect of secreting IFN-γ on autoimmune antibody of myasthenia gravis .

目的 了解重症肌无力患者自身抗体的产生与细胞因子的关系。

The immunoglobulin like anti AChR antibody without complement binding activity is successfully made from a pathogenic anti AChR antibody IgG 637 by site directed mutagenesis.Key words:receptor, cholinergic;myasthenia gravis;point mutation;complement-binding;antibodies

本研究利用定点突变技术,从完型抗乙酰胆碱受体抗体IgG 637制备了不能激活补体的突变型抗乙酰胆碱受体抗体IgG 637/K 322 A,为最终制备出可用于治疗重症肌无力的无补体激活功能的单价抗乙酰胆碱受体抗体提供依据。

It was effective of short-term GC pulse therapy with large dose, in which methylprednisolone took effect most rapidly, with fewest corticoid myathnia.

大剂量激素短期冲击疗法对MG患者疗效肯定,以甲基强的松龙组起效最快,出现一过性肌无力最少。

It was effective of short-term GC pulse therapy with large dose, in which methylprednisolone took effect most rapidly, with fewest corticoid myathnia.

大剂量激素短期冲击疗法对MG 什么患者针灸疗效肯定,以甲基强的松龙组起效最快,出现一过性肌无力最少。

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