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进行性肌萎缩

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In amyotrophic lateral sclerosis, the progressive loss of upper and lower motor neurons leads to respiratory failure, often with predominant diaphragm dysfunction, and death.

目的:在肌萎缩性侧索硬化中,上下运动神经元的进行性丧失导致呼吸衰竭,常伴有明显的膈肌功能紊乱和死亡。

Olfactory ensheathing cell transplantation can improve nerve function in amyotrophic lateral sclerosis patients, and delay progressive aggravation of patients' condition.

嗅鞘细胞移植近期能改善肌萎缩侧索硬化患者的神经功能,延缓病情的进行性恶化。

Objective:To study the characteristic of clinical and laboratory examination of progressive neuromuscular atrophy syndrome.

目的:研究进行性神经性肌萎缩症的临床及实验室检查特点。

This was successful in a mouse model of Duchenne muscular dystrophy.

这一新的递送抗肌萎缩蛋白基因的方法在对杜氏进行性肌营养不良实验鼠的实验中取得了成功。

Results All these infants were characterized by progressive flaccid paralysis in limbs.

结果 婴儿型脊髓性肌萎缩症的主要临床特征为出生后进行性加重的四肢弛缓性瘫痪。

During the past few years, several hospitals employed the mycelium of Ganoderma capens Teng obtained by submerged fermentation by our Institute for the treatment of progressive muscular dystrophy, atrophlic myotonia and certain other related dtseases whih encouraging results.

近年来,我所和有关医院协作,试用深层发酵培养的薄盖灵芝菌丝体治疗进行性肌营养不良和萎缩性肌强直等疾病,发现有一定的疗效。

BACKGROUND: Duchenne muscular dystrophy is a cureless disease, it is a severe result of progressive atrophy of muscle cells, which caused by various defects.

背景:杜氏型肌营养不良的肌细胞损伤并非单一细胞受损,而是多因素缺陷导致肌细胞进行性萎缩的严重后果,患儿一经确诊即被告之无法医治。

The results show that dystrophin protein was produced in the injected muscle and no serious side-effects were observed.

研究者发现在杜氏进行性肌营养不良患者被注射的肌肉组织中有抗肌萎缩蛋白的表达,同时没有发现不良的副作用。

The treated mice had high levels of dystrophin produced in their muscles, including the heart.

接受治疗的杜氏进行性肌营养不良实验鼠的肌肉细胞中中产生了高水平的抗肌萎缩蛋白的表达。

In most cases of mild Becker muscular dystrophy, the number of deleted nucleotides will be a multiple of three.

绝大多数的贝克型进行性肌营养不良患者抗肌萎缩蛋白基因上缺失的核苷酸是三的倍数。

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