肌萎缩侧索硬化(ALS)很少见。
个别患者出现局部肌无力、肌萎缩。
Individual local myasthenia gravis patients, muscular atrophy.
但出现肌萎缩时振幅也变小。
But the amplitude when occurrence amyotrophy also decrescent.
目的探讨神经痛性肌萎缩的临床及护理特点。
ObjectiveTo investigate the clinical features and nursing care of neuralgic amyotrophy.
目的探讨脊肌萎缩症的临床特点和遗传方式。
Objectives To investigate the clinical features and the onset pattern of spinal muscular atrophy.
运动能够引起骨骼肌肥大，防止肌萎缩的发生。
Exercise can lead to skeletal muscle hypertrophy preventing atrophy.
结论：肌萎缩侧索硬化存在神经肌肉接头损害。
Conclusions: there is functional alteration of neuromuscular junction in ALS.
方法分析13例婴儿型脊髓性肌萎缩症患儿的临床资料。
Methods The clinical data of 13 infants suffering from infantile spinal muscular atrophy were analysed.
目的阐明肌萎缩侧索硬化症患者腓肠神经的病理改变特点。
ObjectiveTo investigate the pathologic characteristics of the sural nerve in amyotrophic lateral sclerosis.
目的研究神经肌蒂移植对骨骼肌失神经肌萎缩的预防作用。
Objective To investigate the effect of neuromuscular pedicle transplantation in preventing the atrophy in denervated muscle.
实验结果证实咬肌萎缩后，确实会影响颅颜骨型态及生长发育。
It demonstrated that atrophy of masseter muscle altered the craniofacial growth and development.
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。
AIM: To retrospectively analyze the clinical and electrophysiological features of the peroneal muscular atrophy PMA in 24 cases.
目的：探讨肌内注射糖皮质激素诱导咬肌萎缩的效果及其组织改变。
AIM: to investigate morphologic effect and histological changes of masseter muscle atrophy induced by glucocorticoid with intramuscular injection.
目的探讨肌萎缩侧索硬化症(ALS)F波和神经传导改变的特点。
Objective To investigate the features of F-wave and nerve conduction in patients with amyotrophic lateral sclerosis (ALS).
目的探讨高频正弦波振动对模拟失重条件下大鼠比目鱼肌萎缩的对抗作用。
Objective To study counteracting effects of high frequency vibration on simulated weightlessness-induced atrophy of soleus muscles in rats.
结论全面细致的护理与病情观察有利于神经痛性肌萎缩的恢复，减少并发症。
ConclusionThe careful nursing and observation is very helpful for recover of neuralgic amyotrophy and can decrease complications.
这一新的经过改造的方法，增强了抗肌萎缩蛋白在肌肉细胞内产生的有效性。
This new research modified the introduced dystrophin gene to increase the efficiency of dystrophin protein production in the cells.
肢体远端有肌软弱，肌萎缩，腱反射减退或消失，常有「爪状手」及垂足。
Limbs far end has muscle weakness, amyotrophy, tendinous reflex drops or disappear, often have " ungual state hand " reach hang down sufficient.
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.
什么是肌萎缩型侧索硬化症(ALS)，也称运动神经元症(MND) ？囹。
What is amyotrophic lateral sclerosis (als), also known as motor neurone disease (MND)?
肌活检主要为小群性肌萎缩，ATP酶染色见同型肌群化及肌纤维代偿性肥大。
Muscle biopsy showed: small groups atrophy mainly; extensive fiber type grouping and more hypertrophic fibers by ATP enzyme staining.
目的观察肌萎缩侧索硬化(ALS)的电生理改变，并对其临床意义作初步评价。
Objective to observe the neural electrical pathological changes on amyotrophic lateral sclerosis (ALS) and to evaluate their clinical significance primarily.
吴等人，有效的抗肌萎缩蛋白拯救提高了修改吗啉齐聚心功能的抗肌萎缩缺陷小鼠。
Wu et al, Effective rescue of dystrophin improves cardiac function in dystrophin-deficient mice by a modified morpholino oligomer.
结论：双侧腰大肌不对称及腰大肌萎缩变细可能均是腰椎间盘突出的解剖因素之一。
Conclusion: Both the asymmetry between right and left psoas muscles and the amyotrophy or attenuation of the psoas muscle are probably the anatomical factors which lead to lumbar disc herniation.
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。
Results 22 cases were improved obviously from nerves entrapment syndrome except 2 failure with severe muscular atrophy before the treatment.
MRI无创、敏感和直观的优势使其在肌萎缩侧索硬化的诊断上具有极大应用前景。
With non-invasive, sensitive and macroscopic advantages, MRI has great potentials in the diagnosis of ALS.
结论(1)酒精中毒性肌病临床主要表现为对称性肢带肌萎缩、肌力减退和肌肉疼痛。
Conclusion (1) the main clinical manifestations of chronic alcoholic myopathy are weakness, muscle pain and muscle atrophy, in the proximal parts of the limbs symmetrically.
目的探讨确诊为PMP22大片段重复突变腓骨肌萎缩症（CMT）患者的临床特点。
Objective To analyze the clinical features of CMT patients with PMP22 duplication.
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。
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。
There is loss of anterior horn cells, so that patients present with progressive weakness that proceeds to paralysis from neurogenic muscular atrophy.
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