神经性耳聋

结论：针刺与连续多点脉冲刺激对感觉神经性耳聋患者语言频率听力损失具有确切疗效。

Conclusion Acupuncture and continuous multipoint pulse stimulation has definite therapeutic effect on linguistic frequency hearing loss in the patient of SNHL .

名为Alport综合征的遗传性肾炎。病人通常表现为神经性耳聋及眼病。

This is a type of hereditary nephritis known as Alport 's syndrome in which patients may also manifest nerve deafness and eye problems .

儿童先天性感音神经性耳聋的高分辨率CT和MRI研究

The Study of High Resolution CT and MRI in Congenital Sensorineural Hearing Loss in Children

感音神经性耳聋的MRI诊断

MRI Diagnosis of Sensorineural Hearing Loss

小儿先天性感音神经性耳聋HRCT与MRI诊断价值

HRCT and MRI Diagnoses of Congenital Sensorineural Hearing Loss

方法：报告国内首例经临床确诊的先天性鱼鳞病、感音神经性耳聋、血管化角膜炎的临床、MR表现，并复习文献。

Methods : To report clinical manifestation and MR findings of the first case of keratitis , ichthyosiform , deafness ( KID ) syndrome , and review the literature .

68例感音神经性耳聋患者ASSR测试听阈与ABR测试V波反应阈的相关性研究

A study on the correlation of ASSR and click ABR thresholds in 68 sensorineural subjects

遗传性皮肤病和非综合征型神经性耳聋（nonsyndromichearingimpairment，NSHI）是两大类比较重要的常染色体显性遗传病。

Inherited skin disease and nonsyndromic hearing impairment are two important autosomal dominant diseases .

可以通过ABR、DPOAE组合检测来判断感音神经性耳聋的听力损伤和恢复的程度。

The combination of ABR and DPOAE Can be used to judge the degree of hearing impairment and recovery .

感音神经性耳聋是一类较为常见的疾病，其临床特征基本为气导（AC）、骨导（BC）听力同时下降。

SND is a more common disease . The clinical characteristics of the basic air conduction ( AC ), bone conduction ( BC ) hearing at the same time decreased .

目的评价冠状面CT图像上正常前庭导水管（VA）的特征，为不明原因感音神经性耳聋的诊断进一步提供依据。

Objective To study the imaging features of the normal vestibular aqueduct ( VA ) on coronal CT scans , to provide further evidence for the diagnosis of sensorineural hearing loss of unknown reason .

目的：探讨电针治疗椎动脉型颈椎病（VCS）所致感音神经性耳聋的机理。

Objective : To explore the mechanism of electroacupuncture treating the sensorineural deafness ( SND ) induced by vertebroarterial type cervical spondylosis ( VCS ) .

Waardenburg综合征（Waardenburgsyndrome，WS），是一种以先天性感音神经性耳聋及皮肤、虹膜、毛发的色素分布异常为主要特征的遗传综合征。

Waardenburg syndrome ( WS ) is a type of inherited syndrome characterized by congenital sensorineural hearing loss and hypopigmentation of the skin , iris and hair .

4例8耳获得性感音神经性耳聋和6例4耳听神经瘤者显示蜗神经萎缩变细。结论T2WI/3D/TSE及B-TFE序列能很好地显示耳蜗前庭神经的精细结构；

Conclusion With 3D-TSE and B-TFE sequence the fine structure of cochlear nerve and vestibular nerve lesion can be clearly demonstrated ;

本家系纯音气骨导测试证实为感音神经性耳聋，28例43耳遗传聋经ARI证实为耳蜗性感音性听力损失。

The pure tune audiometry of both air and bone conduct showed neurosensory deafness , and cochlear sensory hearing loss is confirmed in hereditary deafness of 43 ears from 28 cases .

Alport综合征又称遗传性肾炎，患者往往并发肾外综合征，如神经性耳聋和眼疾等。

Alport syndrome ( AS ) is a hereditary kidney disease associated with extrarenal complications , such as sensorineural deafness and eye abnormalities and so on .

目的：分析有症状的婴儿巨细胞病毒（CMV）感染引起的感音神经性耳聋（SNHL）发生率，脑干听觉诱发电位（BAEP）结果与临床特征相关性。

Objective To investigate the incidence of sensorineural hearing loss ( SNHL ) in children with symptomatic cytomegalovirus infection , the relevance between result of the brain stem auditory evoked potential ( BAEP ) and the clinical features .

感音神经性耳聋（SensorineuralDeafness，简称SND）指病变位于螺旋器的毛细胞、听神经或各级听中枢，对声音的感受与神经冲动的传导发生障碍，所引起的听力下降的症状。

Sensorineural deafness ( Sensorineural Deafness , referred to as SND ) lesions were located in the hair cells of Corti , the auditory nerve or auditory central at all levels , barriers to voice the feelings and the transmission of nerve impulses , caused by hearing loss symptoms .

针刺治疗儿童神经性耳聋的临床和实验研究

Clinical and experimental studies on children 's nerve deafness with Acupuncture

为神经性耳聋耳鸣的中医药治疗做出了有益的探索和尝试，丰富了治疗手段。

Valuable exploration for treating nervous deafness and tinnitus were made .

感染性神经性耳聋动物模型的建立及评估

Evaluation and establishment of animal model of infective sensorineural hearing loss

也许神经性耳聋最常见的原因是青年性耳聋。

Perhaps the most common cause of nerve deafness is presbycusis .

听神经瘤，神经性耳聋；

Acoustic neuroma ; Neurous deafness ; Microsurgery ; Facial nerve ;

人神经性耳聋多肽因子样基因克隆和表达分析

Cloning and expression analysis of human dystonia / deafness peptide like gene

小儿极重度感音神经性耳聋助听跟踪4年一例

A 4 year follow-up report of a severe acoustic neuropathy deaf child

突发感音神经性耳聋932例的治疗体会

Experience of treatment about 932 cases of sudden nervous deafness

顺铂致神经性耳聋2例报告

Neural Deafness Following Cisplatin-containing Regimen : Two Cases Report

感音性神经性耳聋听神经细胞变性的中医针灸治疗研究

Research of Acupuncture Treatment of Acoustic Nerve Cytometaplasia Deafness

一母系遗传非综合征型感音神经性耳聋线粒体基因突变分析

Sequence analysis of mitochondrial DNA mutations in a maternally transmitted non-syndromic deafness family

国人connexin26基因突变与先天性感音神经性耳聋的相关性研究

Study of a mutation in connexin 26 gene associated with congenital sensorineural deafness