Xu Ruiyang, an 18-year-old student from Kunming, has suffered from spina muscular atrophy since she was 2 years old.
徐瑞阳是一个来自昆明的18岁学生，他从两岁时就遭受脊柱肌肉萎缩。
Individual local myasthenia gravis patients, muscular atrophy.
个别患者出现局部肌无力、肌萎缩。
Infantile progressive spinal muscular atrophy is an unusual motor neuron disease.
婴儿型进行性脊肌萎缩症是一种少见的运动神经元性疾病。
Objectives To investigate the clinical features and the onset pattern of spinal muscular atrophy.
目的探讨脊肌萎缩症的临床特点和遗传方式。
Methods The clinical data of 13 infants suffering from infantile spinal muscular atrophy were analysed.
方法分析13例婴儿型脊髓性肌萎缩症患儿的临床资料。
Objective To explore measures to prevent motor endplate degeneration and muscular atrophy after motor nerve injury.
目的本研究旨在探讨运动神经损伤后运动终板退变的预防方法。
A gene implicated in spinal muscular atrophy showed an association in three populations, but not in yoruba from ibadan, Nigeria.
一个涉及脊髓性肌萎缩病的基因显示出与三个人群有关联但却没有在伊巴丹、尼日利亚、的优鲁巴人身上发现。
AIM: To retrospectively analyze the clinical and electrophysiological features of the peroneal muscular atrophy PMA in 24 cases.
目的：回顾性分析24例腓骨肌萎缩症的临床与神经电生理特点。
Spinal muscular atrophy in childhood is one of the most common neuromuscular disorders with an autosomal recessive mode of inheritance.
儿童型脊髓性肌萎缩症是常见的遗传性神经肌肉病，为常染色体隐性遗传。
Thomson and others have already created iPS cells from people with ALS, Down syndrome, and spinal muscular atrophy, among other disorders.
Thomson等人已经从ALS（肌萎缩侧索硬化症，译者），唐氏综合症，脊髓性肌萎缩等疾病的患者中构建出iPS细胞。
Results 22 cases were improved obviously from nerves entrapment syndrome except 2 failure with severe muscular atrophy before the treatment.
结果除2例术前有明显肌萎缩者未见恢复外，其余22例术后症状均得到明显改善。
There is loss of anterior horn cells, so that patients present with progressive weakness that proceeds to paralysis from neurogenic muscular atrophy.
存在前角细胞丧失，因此病人表现为渐进性衰弱，这可能因神经源性肌萎缩而出现瘫痪。
Muscular atrophy present reduction of muscle volume in compared with age matched control or the muscle in the same region of the body before the onset of disease.
肌萎缩是骨骼肌容积和同龄人或自身肌肉以前的状态相比出现下降状态的描述。
Objective To investigate the clinical and electrophysiology features of infantile spinal muscular atrophy, and explore the clinical significance of genetic diagnosis.
目的探讨婴儿型脊髓性肌萎缩症的临床、电生理特点及基因诊断的临床意义。
Objective To investigate the clinical and electrophysiology features of infantile spinal muscular atrophy, and explore the clinical significance of genetic diagnosis.
目的探讨婴儿型脊髓性肌萎缩症的临床、电生理特点及基因诊断的临床意义。
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