小脑

Objective: To discuss the molecular mechanism of hereditary cerebellar ataxia in waddles mouse.

目的：探查引起Waddles小鼠遗传性小脑性共济失调的突变基因。

Objective To explore SCA3 gene mutation in the patients with inherited spinocerebellar ataxia.

目的 探讨遗传性脊髓小脑型共济失调病人SCA3基因突变的意义。

Objective To study the gene mutation of the spinocerebellar ataxia（SCA types 1～3 in the patients with primary dystonia.

目的 研究原发性肌张力障碍患者脊髓小脑性共济失调1～3型基因的突变。

Objective To observe the rehabilitation train ing effects of the Frenkel therapy on cerebellar ataxia .

目的观察Frenkel训练法对小脑性运动协调障碍患者的康复治疗效果。

METHODS AND FINDINGS: A boy with ataxia telangiectasia was treated with intracerebellar and intrathecal injection of human fetal neural stem cells.

方法和结果：一名患运动失调性毛细血管扩张症的男孩接受了小脑内和鞘内人胚胎神经干细胞注射治疗。

It is about a girl who has this disease called Spinocerebellar ataxia, where she slowly loses ability to speak and move.

故事是在叙述一个患有脊髓小脑萎缩症的女孩，渐渐的无法说话跟行动。

"Disorders usually produce neuromuscular disturbance s, in particular ataxia."

小脑的损伤或疾病常造成神经肌肉障碍，特别是运动失调。

Br check checks tumour of ministry of horn of cerebella bridge head, the diagnosis of special auditory nerve is very useful.

br检查对小脑桥脑角部肿瘤，特别听神经的诊断是很有用的。

MRI with various sequences has higher diagnosis value in acute cerebral trauma diagnosis,and can make up CT in insufficient diagnosis to the cerebellum,the brain stem,temporal lobe edge contusion and axis cylinder injury,which is worthy of further clinical study and application.

MRI各序列在急性颅脑损伤诊断中具有较高的诊断价值，可弥补CT对小脑、脑干、颞叶边缘挫裂伤及轴索损伤等诊断的不足，值得临床进一步研究和应用。

There are other diseases that lead to cerebellar degeneration, but the loss of Purkinje cells is a clear way to diagnose CA, and the combination of symptoms is sufficiently unique that CA can easily be distinguished from other conditions, even in a living animal.

虽然亦有其他可以导致小脑病变的疾病，但浦肯野细胞的死亡是诊断该疾病的最明确的方法，而且该疾病一系列的症状是非常独特的，因此很容易区别于其他疾病。

She gently rebuff ed him, but agreed that they could be friends

她婉言拒绝了，但同意作为朋友相处。

If in the penal farm, you were sure to be criticized.

要是在劳改农场，你等着挨绳子吧！