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1)  electrically-evoked compound action potential
电诱发复合动作电位
1.
An observation and application of the electrode impedances and electrically-evoked compound action potentials after cochlear implantation using two types of electrodes;
弯、直电极阻抗和电诱发复合动作电位阈值观测在儿童人工耳蜗调试中的应用
2.
[Objective] To observe the change of the electrode impedances and the thresholds of the electrically-evoked compound action potentials in different time points after cochlear implantation and to help for deciding the interval of the mapping.
目的观察人工耳蜗植入后不同时间段的电极阻抗和电诱发复合动作电位(ECAP)阈值的变化,探讨其对调试间隔的指导意义。
2)  Electrically evoked auditory nerve compound action potentials
电诱发听神经复合动作电位
1.
Electrically evoked auditory nerve compound action potentials in Nucleus CI24M cochlear implant users;
Nucleus24型人工耳蜗使用者电诱发听神经复合动作电位的测定
3)  evoked action potential
诱发动作电位
4)  motor-evoked potential
动作诱发电位
5)  Compound action potential
复合动作电位
1.
The effects of muscarinic and nicotinic receptor antagonists on compound action potentials in the cochleae of gerbils;
毒蕈碱和烟碱受体阻断剂对沙鼠耳蜗复合动作电位的影响
2.
The compound action potential (CAP) was recorded and pathologic changes were evaluated with light .
方法 :经耳蜗鼓阶灌注高浓度谷氨酸 (Glu H ,2 0mmol/L ,1 0 μl)、低浓度谷氨酸 (Glu L ,1 0mmol/L ,1 0 μl)后检测不同时点复合动作电位 (CAP)反应阈 ,并观察耳蜗显微和超微结构变化。
3.
The stimulus threshold,maximal stimulus,peak value of compound action potential and refractory period were measured on the toad sciatic nerves after 30 seconds while adding ethanol or acetaldehyde of different concentration with Ringer solution.
将含有不同浓度的乙醇、乙醛的任氏液滴加到蟾蜍坐骨神经表面,30 s后测定神经干刺激阈值、最大刺激值、复合动作电位峰值和不应期等电生理指标。
6)  repetitive compound muscle action potential
重复复合肌肉动作电位
1.
Aim:To observe the electrophysiological characteristics of repetitive compound muscle action potential(R-CMAP)in congenital myasthenic syndrome patients and discuss the significance in diagnosis.
目的:观察先天性肌无力综合征(CMS)患者重复复合肌肉动作电位(R-CMAP)的特征,讨论其诊断意义。
补充资料:运动或动作诱发性癫痫


运动或动作诱发性癫痫
motion or action induced epilepsy

  癫痫的一种。多见于儿童,常在一次突然的动作后诱发癫痫。且大多发生在休息阶段,发作以下肢开始为多,一阵强直性痉挛,可影响及全身,然后局限于动作的肢体。患者意识从不丧失,也无阵挛发生。本病常有遗传倾向,呈显性遗传。
  
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