萎缩症

Methods: Internodal length, the densities of myelinated fiber and unmyelinated fiber, g ratio(axon diameter:fiber diameter) of sural nerves from 7 peroneal muscular atrophy patients were measured and compared between HMSNⅠand Ⅱ.

测定7例腓骨肌萎缩症（遗传性运动感觉神经病，HMSNⅠ和Ⅱ型）患者腓肠神经的节间长度、有髓纤维和无髓纤维的密度以及轴突直径与纤维直径之比，并比较HMSNⅠ和Ⅱ型间上述参数的差异。

Types 1 and 2 myotonic dystrophy are in this category.

肌强直性第一型和第二型进行型肌肉萎缩症（Types 1 and 2 myotonic dystrophy）就属於这一类。

CMT is sometimes called Hereditary Motor and Sensory Neuropathies or Peroneal Muscular Atrophy.

CMT的有时也被称为遗传性运动和感觉神经病变或腓肌萎缩症

Since the age of 12, Sunder's wife, Pradeepa has been fighting pseudohypertrophic muscular dystrophy, or MD, a disease which leads to the gradual weakening of the muscles in the legs and pelvis and that eventually will spread to other areas of the body, to leave her paralyzed.

12岁开始，桑德的太太就是肌肉萎缩症的患者，导致双腿、臀部逐渐无力，最后扩散到全身上下、导致瘫痪，不过尽管知道太太的状况，第一眼在表哥的婚礼遇见她就爱上她，并想跟她结婚。

There is still no effective cure for spinocerebellar degeneration. This again proven that human still lacks of knowledge in brain related matters.

上网找资料后得知后脑萎缩症至今依然没有药方，这再次证实人类对人脑的认识非常贫乏。

Spinocerebellar ataxia is a condition that affects brain functions, such as coordination, speech and balance.Mr. Yang Wengang, who's from Hualien in Taiwan, has the disease. Although he knows his condition is incurable, Yang remains positive, and works hard to give his life meaning. Here is his story.

脊椎小脑萎缩症影响脑部功能，如步伐不协调、语言及平衡功能等，台湾花莲的杨文港就是罹患这种疾病，既使罹患这种无药可医的病，他还是正面面对人生，因为他了解，唯有靠著努力，才能真正感受到自己存在的意义，以下是杨文港的故事。

Spinocerebellar ataxia is an autosomal dominant hereditary neuron disorder disease.

脊髓小脑萎缩症(Spinocerebellar ataxia， SCA)是一种体染色体显性的遗传性神经元退化性疾病。

He suffers spinocerebellar ataxia, or "SCA", a degenerative genetic disease that attacks a person's muscles and their ability to control them.

杨文港跪坐在地上，用双手挖地施肥播种，他罹患脊髓小脑萎缩症，一种渐进性退化性遗传疾病，影响人体肌肉的功能，但杨文港不向命运低头，开创出整片农园。

BACKGROUND: Idiopathic Parkinson's disease can present with symptoms similar to those of multiple system atrophy or progressive supranuclear palsy.

背景：原发性帕金森病表现出与多系统萎缩症或进行性核上性麻痹相似的症状。

We developed an automated image-based classification procedure to differentiate individual patients with idiopathic Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy.

我们采用基于自动影像进行的分类操作以区分个体患者，将患者区分为原发性帕金森病、多系统萎缩症和进行性核上性麻痹。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。