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   deafness children 的翻译结果: 查询用时:0.203秒
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deafness children
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  聋儿童
     The perception limens of pitch difference (df/f) of postlingual deafness adults and prelingual deafness children were 7.78%±6.63% and 14.49%±11.20% respectively,and no significant difference was found between these two groups,but there is significant difference between cochlear implant recipients and contral groups.
     音调差异感知阈 (df/f)在植入人工耳蜗的语后聋成人和语前聋儿童分别为 7.78%± 6 .6 3%和 14 .4 9%± 11.2 0 % ,与各自正常人对照组比较有显著性差异 ; 但两组间无显著性差异。
短句来源
     Methods By means of the programming interface of Nucleus multichannel cochlear implants, the impedance of electrodes was measured during the operation, at initial stimulation, and at each mapping visit of following 3 weeks, using softwares R126 V1.3 and NRT V3.0. Eleven prelingual deafness children implanted with Nucleus devices participated in the study.
     方法在Nucleus多导人工耳蜗编程调试界面上,应用R126V1.3和NRTV3.0软件,测试11例语前聋儿童在不同时期的阻抗值,并进行分析比较。
短句来源
     Objective To investigate the changes of subjective auditory threshold and T-level after cochlear implantation in prelingual deafness children.
     目的调查语前聋儿童人工耳蜗植入术后声场主观测听阈值和对应T值的变化趋势。
短句来源
     To observe the effects of cochlear implant on behavior, ability of social adjustment,and mental state in prelingual deafness children.
     【目的】观察学龄前语前聋儿童电子耳蜗植入术后的行为、社会适应能力及心理状态特点 ,探讨电子耳蜗植入术后是否对儿童的行为问题产生影响。
短句来源
     Objective To construct the music perception testing system for the cochlear implant recipients and to investigate the abilities of music perception of postlingual deafness adults and prelingual deafness children.
     目的 建立测试人工耳蜗植入者音乐感知能力的体系 ,研究语后聋成人和语前聋儿童人工耳蜗植入后对音乐感知的能力。
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  “deafness children”译为未确定词的双语例句
     Results only 4 deafness children aided threshold entered LTASS in ABR test group while 19 childrenin the behavior test group got into the LTASS.
     结果 ABR测试组仅有4例助听听阈进入LATSS(长期平均言语会话谱),而行为测听组有19例助听听阈进入LTASS。
短句来源
     Method High-risk factors were studied in 82 deafness children, with speech and language impediment, by a high-risk scale for parents.
     方法 采用问卷调查的方式对82例聋儿可能存在的危险因素进行回顾性的调查,并对较常见的一些因素进行多因素分析。
短句来源
     ABR of children with pharmacotoxic deafness not beingable to speak at all(their injures were mainly in surrounding nerves mostly)showed symmetrical no wave response,ABR of congenital deafness children not being able to speak at all mostly showed no wave responsetoo.
     但药物中毒性聋是以损害周围神经为主,完全不会讲话者ABR多为双侧无波形。 先天性聋完全不会讲话者ABR亦多无波形。
短句来源
     The results showed that 9 of 11 familial memebers, including 4 normal hearing mothers and 5 streptomycin-induced deafness children had an A to G mutation in 12S rRNA gene of mitochondrial DNA at nucleotide 1555. Two normal hearing fathers had not this mutation.
     结果发现,11例家系成员中有9例(4例为正常母亲,5例为聋哑患儿)线粒体DNA12SrRNA基因上核苷酸1555位点发生了A→G突变。 而2例正常父亲未发现该突变。
短句来源
     Method:High risk factors were studied in 82 deafness children with speech and language impediment by a high risk scale to their parents.
     方法 :采用问卷调查方式对 82例聋儿中可能存在的危险因素进行回顾性调查 ,并对较常见的一些因素在聋儿及配对的正常儿的分布进行多因素分析。
短句来源
  相似匹配句对
     Clinical Analysis of Children Sudden Deafness
     小儿突发性聋临床分析
短句来源
     Causal Analysis of Children's Sensorinerual Deafness
     小儿感觉神经性耳聋的病因分析
短句来源
     Children fushion
     儿童风尚
短句来源
     myopia children
     激光治疗近视 少儿不宜
短句来源
     Mondini's deafness
     小儿Mondini's聋106例报告
短句来源
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This report studied l20children with speech-language disorders by asking their detailed histories,having them examined specially,observing their ABR and acoustic impedance and so on.These results showed that speech-language disorders were obviously related to nervous system disease。ABR of cerebracentric lesions(cerebral dysgenesis,epilepsy etc)children not being able to speak at all was normal or just a little abnormal. ABR of children with pharmacotoxic deafness not beingable to speak at all(their injures were...

This report studied l20children with speech-language disorders by asking their detailed histories,having them examined specially,observing their ABR and acoustic impedance and so on.These results showed that speech-language disorders were obviously related to nervous system disease。ABR of cerebracentric lesions(cerebral dysgenesis,epilepsy etc)children not being able to speak at all was normal or just a little abnormal. ABR of children with pharmacotoxic deafness not beingable to speak at all(their injures were mainly in surrounding nerves mostly)showed symmetrical no wave response,ABR of congenital deafness children not being able to speak at all mostly showed no wave responsetoo.

对120例言语。语言障碍的患儿(完全不全讲话者91例,会讲几句短语者12例,仅会讲单词者17例),经过详细询问病史,听力检查如听性脑干反应(ABR)及声导抗测试,其中部分病例还经过神经科、小儿内科医生查均无证实言语-语言障碍与神经系统病变有明显关系。结果表明:大脑中枢病变(大脑发育不全、颅脑外伤、脑性脑瘫、癫痫等)完全不会讲话患儿,ABR反应阈多正常或在轻度异常范围。但药物中毒性聋是以损害周围神经为主,完全不会讲话者ABR多为双侧无波形。先天性聋完全不会讲话者ABR亦多无波形。

Mitochondrial DNA of peripheral blood from 11 members of 4 streptomycin-induced deafness families was analysed using PCR-SSCP and PCR-BsmAI digestion. The results showed that 9 of 11 familial memebers, including 4 normal hearing mothers and 5 streptomycin-induced deafness children had an A to G mutation in 12S rRNA gene of mitochondrial DNA at nucleotide 1555. Two normal hearing fathers had not this mutation. Thus, we speculated that this mutation is a molecular basis for human genetic susceptibility to...

Mitochondrial DNA of peripheral blood from 11 members of 4 streptomycin-induced deafness families was analysed using PCR-SSCP and PCR-BsmAI digestion. The results showed that 9 of 11 familial memebers, including 4 normal hearing mothers and 5 streptomycin-induced deafness children had an A to G mutation in 12S rRNA gene of mitochondrial DNA at nucleotide 1555. Two normal hearing fathers had not this mutation. Thus, we speculated that this mutation is a molecular basis for human genetic susceptibility to streptomycin-induced deafness. The pathogenetic mechanism of the susceptible deafness was also discussed preliminarily in this paper. This study is of significant value for clinical gene diagnosis and prevention.

为在分子水平探讨链霉素致聋的病理机理,采用PCR-SSCP及PCR-限制性内切酶酶切,对4个链霉素致聋家系11例成员的外周血线粒体DNA进行了分析。结果发现,11例家系成员中有9例(4例为正常母亲,5例为聋哑患儿)线粒体DNA12SrRNA基因上核苷酸1555位点发生了A→G突变。而2例正常父亲未发现该突变。推测该突变是人体对链霉素致聋遗传易感性的分子基础。并对易感致聋的发病机理进行初步探讨。本研究对临床基因诊断及预防具有指导意义。

The real ear insertion gain measrement is one of methods in hearing aids fitting.Two pre selection formula (NAL R,two thirds) of prescriptive strategy had been applied to children (15 subjects,30 ears) with severe and profound sensori neural hearing loss,meanwhile,the comparison had been made at several frequencies in two aspects such as target gain and real ear insertion gain.The result indicated the more effective formula seemed to be two thirds,and NAL R formula appeared to be less effective on...

The real ear insertion gain measrement is one of methods in hearing aids fitting.Two pre selection formula (NAL R,two thirds) of prescriptive strategy had been applied to children (15 subjects,30 ears) with severe and profound sensori neural hearing loss,meanwhile,the comparison had been made at several frequencies in two aspects such as target gain and real ear insertion gain.The result indicated the more effective formula seemed to be two thirds,and NAL R formula appeared to be less effective on hearing compensation in our study.Yet individulization must be emphasized and the type of the audiogram should be taken into consideration. [Chinese Arch Otolaryngol Head Neck Surg,2000;7(2):67~69 From the Rehabilitation Research Center of China for Deafness Children,Beijing 100029 (Dr.Li Ju)]

真耳介入增益法是助听器常用的验配方法之一。本文应用 NAL -R、2 / 3增益公式 ,对感音神经性耳聋听力损失程度为严重聋和极度聋的聋儿 ( 1 5人 3 0只耳 ) ,进行了助听器验配 ,并对不同频率上的目标增益值、真耳介入增益值方面进行了比较 ,探索适合于这类患者的最佳预选公式。结果发现助听效果最好的是 2 / 3增益公式 ,助听效果最差的是 NAL-R公式 ,但在应用时要强调个体化。

 
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