共济失调

Results: the protocol has been applied at present to 29 cases, from a woman of 84 yo. diagnosed as alzheimer phase IV in 2002 with aphasia, agnosia, apraxia, continuos repetitive oscillating and like-parkinson movements, dysfunction of all sensorial recognition system, without sphincters control, to a 49 yo.

结果：这个干预方案被应用于29例病人，这其中包括年龄84岁的老年女性，该患者在2002年被诊断为&阿尔采木病4期&，有失语、失认、共济失调、持续的帕金森样的震颤运动、整体感觉系统功能障碍以及括约肌功能障碍。

Results The clinical manifestation for these cases are specifically showed as slow and deepen supply imbalance,pyramidon,pyramid bean and brain function injured disease status and eye-ball barrier,etc.

结果 临床突出特点为缓慢进行性加重的共济失调、锥体外系、锥体束、大脑高级功能受损症状及眼球运动障碍等。

Results The clinical manifestation for these cases are specifically showed as slow and deepen supply imbalance,pyramidon,pyramid bean and brain function injured disease status and eye-ball barrier,etc.

结果 临床突出特点缓慢进行性加重的共济失调、锥体外系、锥体束、脑高级功能受损症状及眼球运动障碍等。

Of all, 5 cases received operation. All cases were fasted for average 25.8 days (1046 days) and displayed absentmindedness and faintness, with 7 cases with nystaxis, 6 with ataxia, 3 with retrograde amnesia and 2 with disorientation. Besides the combined therapy of SAP, thiamine was given in full dosage.

SAP禁食时间长(超过2周)，全部患者长期禁食后平均25.8 d(10～46 d)均表现精神恍惚，神志淡漠，其中眼球震颤7例，共济失调6例，逆行性遗忘3例，定向力障碍2例。

The authors describe the four patients in the first known Belgian family with autosomal recessive spastic ataxia of Charlevoix–Saguenay.

比利时发现第一个常染色体隐性遗传的Charlevoix–Saguenay痉挛性共济失调家系，共有4个患者。

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。