英语人>网络例句>mind deafness 相关的网络例句
mind deafness相关的网络例句

查询词典 mind deafness

与 mind deafness 相关的网络例句 [注:此内容来源于网络,仅供参考]

Results:92 patients (113 ears) were examined by PTHT, AI , 40 Hz AERP,ABR and DPOAE. It was found that organic deafness was confirmed on 98 ears (86.73%), of which exaggerated hearing loss was 38 ears; nonorganic deafness was confirmed on 13 ears (11.50%); stimulated deafness was 2 ears(1.77%). 98 organic deafness ears were diagnosed, of which conductive hearing loss was 25ears; sensorineural hearing loss was 29 ears, and mixed hearing loss was 44 ears.

结果: 92例患者113耳行纯音听阈测试、声导抗、40 Hz AERP、ABR与DPOAE检测,发现器质性聋98耳,占86.73%,其中夸大性聋者38耳,夸大程度<20dBnHL6耳,20~40dBnHL27耳,>40dBnHL5耳;非器质性聋13耳,占11.50%,诈聋2耳,占1.77%;98耳器质性听力损失者中,25耳为传导性耳聋,29耳为感音神经性耳聋,44耳为混合性耳聋。

Deafness which occurs at birth is called congenital deafness and that which occurs after birth is called adventitious deafness.

耳聋发生在出生时被称为先天性耳聋,并在出生后发生的被称为偶然耳聋。

All were determined by the acoustic immitance audiometer and pure tone audiometry. Results (1)A type was determined in 33 patients (62.26%), As type in 4 patients (7.55%), B type in 2 patients (3.77%), and C type in 14 patients (26.42%). 35 patients (66.04%) had normal air hearing threshold, 16(30.19%) had a little deafness and 2 (3.77%) had middle deafness.

结果 (1)53例患者中,声阻抗鼓室导抗图A型33例(62.26%),As型4例(7.55%),B型2例(3.77%),C型14例(26.42%);正常听阈35例(66.04%),轻度聋16例(30.19%),中度聋2例(3.77%);(2)As、B、C型异常导抗图、峰压值、同侧对侧镫骨肌反射、坡度在鼻窦炎各分型与对照组、各分型之间比较,30组比较中9组有统计学差异。

Result: The result showed that the prevalence rate of noise induced deafness was 27.97%,there was a dose response relation between the incidence of noise induced deafness and the doses of the noise exposure.

结果:结果表明,所调查五金工业噪声作业工人噪声性耳聋患病率为27.97%,各级噪声性耳聋患病率与噪声接触剂量之间存在着剂量反应关系。

The result showed that the prevalence rate of noise induced deafness was 27.36%,there was a dose-response relation between the incidence of noise induced deafness and the doses of the noise exposure.

研究结果表明,所调查麻纺厂噪声作业工人噪声性耳聋罹患率为27.36%,各级噪声性耳聋罹患率与接触噪声剂量之间存在着剂量反应关系。

In this family,deafness is maternally inherited and all the sufferers have the mitochondrial DNA 12s RNA A1555G mutation. Four methods are used in the experiments for establishing immortal lymphoblastoid cell lines of the family with non-syndromic deafness.

该家系患者呈典型的母系遗传特征,且研究发现患者中均具有线粒体DNA 12s RNA A1555G突变,是迄今世界上最大的非综合征耳聋家系之一,在该家系的建系过程中使用了4种不同的方法。

Kai Bao vegetation," it reads: Scorpio treatment of various rubella and stroke, hemiplegia, Kouyanwaixie, language astringent, hand-foot-pumping;"Compendium of Mat eria Medica" narrative:"scorpion dry body, its sweet Sim, Xing Ping" is the treatment of large Kashin-Beck disease and leprosy medicine;"Yu Catalpa drug solution," said the Scorpio can "wear bars Speranskia tuberculata, except by the wet wind";"outline": governance adults Xuan malaria, deafness, hernias, various wind sores, women vaginal discharge Yam off;" Mat eria Medica truth," hand of liver Qufeng recorded Scorpio, where the children tire high spirit twitch, adult hemiplegia, deafness and so no need of;"TCM Dictionary" Scorpio has a "Xifeng antispasmodic, anti-inflammatory attack drugs, Tongluo pain feature.

开宝草木》记载:全蝎疗诸风疹及中风、半身不遂、口眼歪斜、语涩、手足抽;《本草纲目》叙述:&蝎的干燥体,其味甘辛、性平&,是治疗大骨节及麻风病的良药;《玉楸药解》称全蝎能&穿筋透骨、逐湿除风&;《纲目》:治大人痃疟,耳聋,疝气,诸风疮,女人带下,阴脱;《本草求真》记载全蝎专人肝祛风,凡小儿胎风发搐,大人半身不遂、耳聋等无不用之;《中药大辞典》全蝎具有&熄风镇痉、消炎攻毒、通络止痛&功能。

Deafness is an etiologically heterogeneous trait with many known genetic, environmental causes or a combination thereof. The identification of more than 120 independent genes for deafness has provided profound new insights into the pathophysiology of hearing.

耳聋有着复杂的病因学特点,遗传和/或环境因素均可致聋。120 多个耳聋相关基因的发现为我们了解听觉的病理生理机制提供了新的视点。

Results Nine of 10 patients had conductive deafness and 1 mixed deafness. Obvious neoplasm was observed under indirect laryngoscopy or fiberoptic pharyngorhinoscopy.

结果电测听显示传导性耳聋9例,混合性耳聋1例;鼻咽镜或纤维鼻咽镜检查发现局部有明显新生物,病理学检查证实10例患者中,鼻咽癌Ⅰ期、Ⅳ期各2例,Ⅱ期、Ⅲ期各3例。

Because Cx43 gene is the first a connexin gene to be associated with non-syndromic deafness, we have sequenced the coding region of Cx43 gene from 190 Taiwanese patients with prelingual deafness and 130 unrelated normal individuals.

Cx43基因是connexin α家族中第一个被发现与非症候群听障有关的基因,我们收集台湾地区190位语言学习前期听障患者,及130位听力正常人血液DNA做Cx43基因的分析。

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