肌萎缩

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。

Methods: Medical records, including clinical presentations, lab analysis, electromyography, muscle biopsy, therapy and prognosis, of 4 primary hyperparathyroidism with amyotrophy patients admitted in our hospital from 1990 to 2006, were retrospectively reviewed in comparison with the literatures.

回顾性分析1990年至今在我科诊治的以肌萎缩和肌无力为首发症状的甲旁亢病例共4例，就其临床表现、实验室检查、电生理特点、组织学变化以及治疗预后结合文献进行分析。

Previous studies in the mdx mouse model of muscular dystrophy demonstrate that inhibiting myostatin attenuates several features of dystrophic muscle.

肌营养不良症小鼠模型mdx的前期研究中发现抑制myostatin可以改善肌萎缩。

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 four cases of Hirayama disease occured in adolescents,three were male,one was female,characterized by muscular atrophy in the hand and forearm with ulnar muscles worsening;the brachioradial was spare.Fine postural tremor （4 cases） and cold paresis （3 cases） were demonstrated.

结果 4例患者有3例为青春期男性，1例为青春期女性，主要表现为局限于手和前臂的肌萎缩，尺侧肌肉萎缩较重，上肢呈斜坡样。4例手指伸展时出现震颤；3例伴寒冷麻痹。

The proliferation of thyroarytenoid muscle and lateral cricoarytenoid muscle cell of dog remained at high level in 5 months after denervation and then slowed down and atrophy of muscles occurred 6 months after denervation.

甲杓肌及环杓侧肌失神经支配后5个月内保持高增殖水平，以后均降低，失神经支配6个月后肌萎缩开始明显。

OBJECTIVE: To explore effects of muscle-derived stem cell transplantation on denervated gastrocnemius atrophy.

目的：探讨大鼠肌源性干细胞移植对失神经腓肠肌萎缩进程的影响。

Muscular atrophy ; myoparalysis ; postpoliomyelitis syndrome ; surgery ; operative

肌萎缩；肌瘫痪；脊髓灰质炎后综合征；外科；手术

Background and Objective Pseudohypertrophic muscular dystrophy is a kind of lethal X-chain recessive inherited disease. The etiological factor is mainly due to gene mutation of Xp21 which induce the structural and functional abnormality of a kind of cell skeleton protein: dystrophin.

背景和目的假肥大型肌营养不良症(pseudohypertrophic muscular dystrophy，PMD)是一种常见的致死性X-连锁隐性遗传病，病因主要是由于X染色体短臂2区1带(Xp21)的基因突变而导致一种细胞骨架蛋白——抗肌萎缩蛋白的结构和功能异常所致。

Aim To study the preventive and therapeutic effects of Buyang Huanwu Decoction on denervated tibial muscle atrophy of rats.

目的 研究补阳还五汤对大鼠胫前肌失神经肌萎缩的防治作用。

But we don't care about Battlegrounds.

但我们并不在乎沙场中的显露。

Ah! don't mention it, the butcher's shop is a horror.

啊！不用提了。提到肉，真是糟透了。