肌萎缩的

Hirayama disease should be considered for young patient,especially male patient,with asymmetrical amyasthenia and amyotrophy in the hand and forearm.Hirayama disease can be diagnosed if MR abnormalities of the lower cervical dural sac and spinal cord are seen in a fully flexed position.

当遇到青少年出现手及前臂不对称的肌无力和萎缩而无感觉障碍时，应首先考虑有平山病的可能，可进一步行屈颈MR检查，出现下颈髓及其硬膜囊的特征性表现可确诊。

The patient showed atrophy in frontal and temporal lobe on regular MRI, significantly reduced amount of Nacetyl aspartic acid、cholineand creatinecompared with contralateral on MRS , remarkably decreased blood flow in the left temporal polar and front part of fontal lobe compared with contralateral on PWI. There were decreased association fibers between Broca and other regions meanwhile no association fibers were found between triangular area and wernicke region on DTI. The fibers projecting to opercular part of frontal lobe via archiform fibers were lessened. The mean FA and fibers of Broca and Wernick regions were less than that of the healthy subjects.

常规MRI显示左侧额叶及颞叶萎缩；磁共振波谱分析显示左侧颞叶和额叶N乙酰天门冬氨酸、胆碱、肌酸含量较对侧明显减低；磁共振灌注成像显示左侧颞极及额前部的血流量较对侧减低；弥散张量成像显示左Broca区与其他脑区间纤维联系减少，三角区与Wernicke区无纤维联络，左侧Wernicke区通过弓状纤维到达额叶岛盖部的纤维减少，Broca及Wernicke区平均FA及纤维束较正常人减少。

Objective To investigate the changes of cell proliferation state after denervation of laryngeal adducent muscles in dog.Methods The muscles were obtained from 8 dogs with recurrent lanyrgeal nerves injured.

目的 了解犬喉内肌失神经支配后细胞萎缩和增殖状态的变化规律，对反映肌肉不可逆改变的指标进行初步探讨。

Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset.

受感染的人可以有睡眠紊乱，个性改变，共济失调，失语症，视觉丧失，物理，肌肉萎缩，肌阵挛，进行性痴呆等症状，并且会在发病的一年内死亡。

Six of 8 SBMA patients showed myogenic changes together with the neurogenic atrophy in their muscle biopsy.

研究8例SBMA患者和3例女性携带者的骨骼肌活检组织，结果6例SBMA患者和全部女性携带者显示了肌源性的变化并伴有神经元性的萎缩。

Myotonic MD's age at onset: 20 to 40 years Myotonic muscular dystrophy is the most common adult form of muscular dystrophy.

强直性海事处发病年龄：从20到40岁强直性肌营养不良症是最常见的成人形式的肌肉萎缩症。

Myotonic MD's age at onset: 20 to 40 years Myotonic muscular dystrophy is the most common adult form of muscular dystrophy.

强直性海事处发病年龄：从20到40岁强直性肌营养不良症是最常见的大人形式的肌肉萎缩症。

A disorder due to a similar molecular basis, myotonic dystrophy 1 (DM1), is known to have white matter hyperintensities on cranial MRI.

另一种有类似分子病理学基础的疾病：萎缩性肌强直(DM1)患者的核磁共振成像也有白质高信号。

Hot Springs has a very rich mineral resources of temperature, water temperature as high as 76 ° C, spring water is rich in iron, sulfur, radon, calcium, magnesium and other 48 kinds of minerals wholesome for nerve pain, rheumatism , lumbar muscle strain, muscle atrophy, gastroenterology and many other diseases with significant efficacy;泡浴can often skin beauty, beauty fitness.

龙门温泉有十分丰富的温矿泉水资源，水温高达76°C，泉水富含铁、硫、氡、钙、镁等48种有益身心的矿物质元素，对神经性骨痛、风湿病、腰肌劳损、肌肉萎缩、肠胃病等多种疾病有显著疗效；经常泡浴能护肤美容、养颜健身。

Inherited disease of muscle degeneration, characterized by weakness and progressive atrophy of the skeletal muscle.

肌肉营养不良：遗传性的肌退化。特徵是脆弱和渐进的骨骼肌萎缩。

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。