基本释义:

心因性聋

网络释义

1)psychogenic deafness,心因性聋

2)Deafness gene,耳聋基因

3)Deafness/etiol,聋/病因学

4)mental deafness,心理聋

5)Sudden hearing loss,突发性聋

6)Presbycusis

[,prezbi'kju:sis,,presbi'kju:sis],老年性聋

用法和例句

The DPOAEs in recovery course of sudden hearing loss;

突发性聋恢复过程中畸变产物耳声发射的变化

The Electron under the laryngoscope the eustachian tube drum room injection Dexamethasone treatment sudden hearing loss

电子咽喉镜下咽鼓管鼓室注入地塞米松治疗突发性聋

Objective:To studay clinical of sudden hearing loss patients in the treatment of routine medicine and on the base of it add acupuncture holographic points and the points around ear.

目的:观察在常规药物基础上加用全息穴及耳周腧穴针刺治疗突发性聋患者的临床疗效。

Mitochondrial DNA~(4568)deletions in guinea-pig associated with presbycusis;

豚鼠线粒体DNA~(4568)缺失与老年性聋的关系

Antagonism of melatonin on presbycusis in guinea pigs;

褪黑素对豚鼠老年性聋的拮抗作用

Detection of auditory brain stem response in patients with presbycusis;

脑干听觉诱发电位检测老年性聋

Deafness Gene Chip for 153 Cases of Hearing Impairment Patients Testing;

153例耳聋患者的耳聋基因芯片检测

Molecular Epidemiology Investigation of Common Deafness Genes in Deafness Patients of Different Ethnic Origins in Northwest China

中国西北不同民族耳聋患者常见耳聋基因分子流行病学研究

Analysis of deafness gene mutations by gene chip and its clinical significance

遗传性耳聋基因芯片检测及其临床意义

Establishment and Application of Mutation Screening System Based on DHPLC for Hereditary Deafness;

基于DHPLC的遗传性耳聋基因突变检测平台的建立和应用

Screening for GJB2 deafness gene mutations by denaturing high performance liquid chromatograph

变性高效液相色谱法筛查间隙连接蛋白2耳聋基因突变

Gene Localization and a Novel Mutation Identified for Non-syndromic Hearing Loss;

常染色体显性遗传非综合症型耳聋基因的定位与突变筛查

Genetic Counseling and Prenatal Diagnosis for Hearing Loss Based on Genetic Testing;

基于基因诊断的耳聋遗传咨询与产前诊断

Clinical Evaluations and Mutational Analysis for Late-onset Progressive Hearing Loss;

迟发性耳聋临床表型特征及基因突变分析

Collecting, Characterizing of the Genetic Resource and Molecular Mapping of the Relevant Genes for Hereditary Hearing Impairment;

遗传性耳聋家系的收集、保存及基因定位研究

Mutations in the GJB2 Gene in Henan Patients with Prelingual Non-syndromic Hearing Impairment;

河南地区非综合症型耳聋患者GJB2基因突变分析

The Experimental Study for the Treatment of Noise Deafness by Transferring Gene Hath1 into Cochlea;

Hath1基因内耳导入治疗噪声性聋的实验研究

SLC26A4 IVS7-2A>G gene mutation in hereditary hearing loss families

遗传性耳聋家系的SLC26A4 IVS7-2A>G基因突变分析

Mutation analysis of GJB2 gene in deaf population from Chongqing city

重庆市非综合征型耳聋患儿GJB2基因突变分析

Molecular genetic analysis of the mtDNA A1555G mutation in patients with non-syndromic hearing loss

非综合征型耳聋线粒体基因A1555G突变分析

HRCT Analysis of Inner Ear Malformation and Deafness Gene Mutations in Chinese Pedigrees with SNHL

内耳畸形HRCT影像学研究及SNHL家系耳聋相关基因的检测

Perhaps the most common cause of nerve deafness is presbycusis.

也许神经性耳聋最常见的原因是青年性耳聋。

Protection of NT3 gene transfection on the guinea pig cochlea treated with gentamicin

神经营养因子3基因转染对庆大霉素性耳聋保护作用的实验研究

The Change of Cochlear Cells Apoptosis and Its Related Genes' Expression in Guinea Pig Following Lower Intensity Blast Deafness;

豚鼠低强度爆震聋后耳蜗细胞凋亡及其相关基因表达的变化