Hearingloss相关论文
Causal Variants of the GJB6 Gene are Associated with Hearing Loss and Skin Manifestations: A Case Re
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Gout is the most common cause of monoarthritis in men occurring classically in the great toe and the knee.Extra-articula......
突发性感音神经性聋(sudden sensorineural hearing loss, SSNHL)是指在72 h内突然发生的原因不明性感音神经性听力损失，至少在3个......
Hereditary sensorineural hearing loss in Chinese Rongchang pigs result from promoter mutations in MI
(Background)Genesis of novel gene regulatorymodules is largely responsible formorphological and functional evolution.New......
目的 对无自觉症状噪声暴露作业者进行了常频与高频测试检查，以期发现他们的隐性噪声性听力损害情况，并连续观察噪声对听力损害变化......
SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic midfrequency hearing
Hearing impairment is considered one of the most prevalent clinic disability worldwide.The variety of hearing impairment......
Objective To analyze the characteristics of hearing loss for noiseexposed workers in iron and steel industry.Methods A r......
Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive non-syndromic
Background: Autosomal recessive non-syndromic hearing loss (ARNSHL) is highly heterogeneous, and transmembrane channel-l......
Objective mitochondrial DNA (mtDNA) mutation are one of the important causes of deafiness.In particular, the 12S rRNA ge......
The effect of hearing aids amplification on auditory plasticity: Electrophysiological and perceptual
Approximately one-third of people over 65 year-old have a hearing loss.With the presently aging population,the prevalenc......
Increased Endothelial Progenitor Cell Circulation and VEGF Production in a Rat Model of Noise-Induce
Objective: Noise-induced hearing loss has been associated with alterations in cochlear blood flow.This study analyzed th......
Objectives Non-syndromic hearing loss is the most common neurosensory deafness where majority of patients have largely d......
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Analysis of p.V371 compound heterozygous mutations in the GJB2 gene in Chinese infants and young chi
The p.V371 (c.109G>A) mutation in the GJB2 gene is the most frequent cause of congenital deafness;however,its pathogenic......
Targeted genomic capture and massively parallel sequencing to identify novel mutations causing hered
Background: Hereditary hearing loss is genetically heterogeneous, and hundreds of mutations in than 60 genes are involve......
Tinnitus,acute or chronic,is one of the most common and refractory disorders.Acute tinnitus is a symptom that is a warni......
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GJB2 (Cx26) gene mutations in Chinese patients with congenital sensorineural deafness and a report o
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Associations of blood pressure and arterial compliance with occupational noise exposure in female wo
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Background:Acute acoustic trauma (AAT) is an acute hearing impairment caused by intense noise-impact.The current managem......
目的初步评估粘贴式骨导助听器对单侧外耳道骨性闭锁患儿双耳聆听效应及主观满意度的影响。方法2019年1—8月就诊于首都医科大学附......
随着技术的不断革新，基因组学及其他组学技术，如转录组学、蛋白质组学、代谢组学，日益成为精准医疗的重要基础。目前职业性噪声听力损......
The association between occupational noise exposure and hypertension is unclear.We aimed to explore the association ......
The Association between Noise Exposure and Cardiovascular and Hearing Abnormality among Industrial W
Objectives:In order to estimate the current prevalence of hypertension,cardiovascular condition and hearing difficul......
Sphingosine-1-phosphate (S1P) is a biologically active lysophospholipid.Spinster homolog 2 (Spns2) acts as an S 1P t......
Disruption of the autism-related gene Pak1 causes stereocilia disorganization,hair cell loss,and dea
Several clinical studies have reported that hearing loss is correlated with autism in children.However,little is known a......
目的探讨2017至2019年武汉市部分汽车制造业工人职业噪声接触及其听力损失情况。方法于2020年5月，采用横断面方法选择2017至2019年......
目的：评价耳聋儿童助听后1年内听觉及言语能力发展变化趋势，探讨耳聋程度对聋儿的听觉及言语发育水平的影响，为聋儿的有效康复提供临......
目的：通过分析突聋伴眩晕患者焦虑和抑郁状态及影响因素,为有效治疗提供客观依据。方法：收集80例单耳突聋伴眩晕患者（突聋伴眩晕组）、8......
Superoxide dismutase 2(SOD2)-mediated gene therapy has significant protective effects against kanamycin-induced hearing ......
目的：通过描述、分析在使用吉非替尼或厄罗替尼过程中出现听力减退的5例晚期非小细胞肺癌患者的临床特征及听力损害表现，揭示两药与......
1 为什么要进行耳聋检查rn耳聋是临床上最常见的遗传性疾病,由遗传性因素导致的约占60%左右;2006年第二次残疾人抽样调查显示,我国......
To observe the changes of the content and distribution of cochlear actin in growing rats at different periods of iron de......
Adenovirus-mediated human β-nerve growth factor gene transfer has a protective effect on cochlear sp
Objective: To study whether adenovirus-mediated human β-nerve growth factor (Ad-hNGFβ) gene has any protective effect ......
突发性感音神经性聋（突发性聋）为耳科常见急症之一，目前病因学说较多，公认的为内耳循环障碍和病毒感染。但由于病因尚不明确，因此治疗方......
目的 探讨不同剂量糖皮质激素在急性低频下降型感音神经性聋治疗中的疗效.方法 将60例急性低频下降型感音神经性聋患者按糖皮质激......
目的对比分析耳后注射甲泼尼龙琥珀酸钠与全身静脉应用地塞米松治疗突发性聋的疗效。方法选取58例单侧突发性聋患者，按随机单盲法随......
目的 对听力初筛未通过的新生儿进行聋病易感基因筛查,探讨新生儿听力联合基因筛查的意义.方法 应用飞行时间质谱技术,对622例听力......
目的 了解湖南省不同地区听力筛查工作状况,为新生儿听力筛查工作深入开展提供指导.方法 统计分析湖南省三个地区2010年10月1日-20......
目的分析老年突发性耳聋的临床资料并探讨其预后情况。方法收集2010年12月至2015年12月本院耳鼻喉科住院的老年突发性耳聋患者病例......
目的 分析急性低频感音神经性聋(ALHL)患者的伴随症状以及影响预后的相关因素.方法 对57例(67耳)ALHL患者听力损伤程度、眩晕情况......
