Deafness相关论文
目的:通过对3个n PTPN11基因突变的综合征型耳聋家系的临床表型和基因进行分析，了解其分子生物学病因。n 方法:对2019年1......
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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......
Down-regulation Of Msrb3 And Destruction Of Normal Auditory System Development Through Hair Cell Apo
Hearing defects can significantly influence quality of life for those who experience them.At this time, 177 deafness gen......
Down regulation of deafness gene Msrb3 can seriously impair the normal otic development in zebrafish
aring defects have a very serious impact on human health.Until now,143 loci have been mapped and 62 genes have been foun......
Objectives: To verify the clinical validity and accuracy of DNA microarray kit for genetic testing of 15 target deafness......
The cochlear implant and possibilities for narrowing the remaining gaps between prosthetic and norma
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Analysis of the ratio of mitchondrial DNA with A1555G mutant to wild type in deaf patients of Fujian
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COVID-19 is a systemic infectious disease caused by the new SARS-CoV-2 coronavirus. The COVID-19 pandemic has caused soc......
Objective:To observe the clinical effect of hyperbaric oxygen in the treatment of sudden deafness.Methods:Ninety-six pat......
Migraine is one of the most common and highest burdens of disease.As a primary cerebral dysfunction illness,migraine mig......
Key facts Synonym:Siderosis.Definition:Hemosiderin staining of leptomenginges following repeated subarachnoid hemorrhage......
：Objective To detect mitochondrial gene 3243A to 1507Chinese and analyze their clin ical characteristics．Methods Clas－sical......
The mutations of CARD15 gene and clinical features of Chinese patients with Blau syndrome were analyzed. We identified10......
Objective To study effects of Jiangtang Fanglong Wan (glucose-lowering and deafness-preventing capsule) on hearing in an......
A novel mitochondrial tRNA gene mutation in a chinese family with dilated cardiomyopathy and sensori
Objective: To determine whether a mutation of mitochondrial DNA induces familial dilated cardiomyopathy in Chinese famil......
突发性聋(sudden deafness)是突然发生的原因不明的感音神经性聋,其发病率约5人/10万～20人/10万,近年来有增加趋势,多见于40岁以上......
人们都希望自己聪明。但到底有多少人真正理解“聪明”的含义呢?按照中国传统的说文解字:聪者,听也,明者,清也。耳聪才能目明,大脑......
This paper presents a wideband frequency-shift keying (FSK) demodulator suitable for a digital data transmission chain o......
Heteroplasmy Level of the Mitochondrial tRNA~(Leu(UUR)) A3243G Mutation in a Chinese Family Is Posit
Objective To investigate the mutations of mitochondrial genome in a pedigree with suspected maternally inherited diabete......
目的 比较不同剂量地塞米松治疗急性低频下降感音神经性聋(ALHL)的临床疗效.方法 266例ALHL患者按就诊顺序分为治疗组(136例)与对......
目的探讨突发性聋患者外周血中性粒细胞水平与患者预后的关系。方法将160例突发性聋患者进行纯音听阈测定听力损失，分型进行治疗，同......
目的探讨法舒地尔联合脑苷肌肽治疗2型糖尿病并耳鸣耳聋的临床疗效。方法选取2016年1－12月大同市第五人民医院收治的2型糖尿病并耳......
目的：应用遗传性耳聋基因芯片对非综合征型耳聋患者进行分子病因学检测，评估其在遗传性耳聋快速基因诊断中的可行性。方法：采集96例耳......
目的通过对初生婴儿聋病易感基因的普遍筛查,了解其分子流行病学特点,为完善防聋策略提供依据。方法随机选择1 902名生后3~5d的新......
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 制备治疗耳聋的多肽类药物神经生长因子(NGF)温度敏感缓释凝胶给药系统并考察其体外释放规律,为内耳疾病治疗中的大分子药物......
目的 探讨影响突发性耳聋治疗效果的相关因素.方法 回顾性分析133例(148耳)突发性耳聋患者的临床资料.结果 133例患者经系统治疗后......
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......
目的 研究经耳道鼓室置管灌注甲泼尼龙治疗难治性突发性聋的安全性和有效性.方法 选择难治性突发性聋患者68例,按随机数字表法分为......
目的 探讨突发性耳聋患者的预后相关因素.方法 回顾性分析137例(149耳)突发性耳聋患者的临床资料.观察患者年龄、发病至就诊时间、......
1例11岁男性患儿因支气管肺炎给予注射用阿奇霉素(0.5 g静脉滴注、1次/d，每次滴注3 h)和注射用头孢替安(1.0 g静脉滴注、3次/d)抗感......
耳聋是影响人类健康的主要疾病，其病因复杂，遗传因素占50％以上。近年来基因诊断技术的不断发展，尤其是基因芯片等高通量检测技术的快速......
目的 观察泛影葡胺治疗突发性聋的临床疗效及不良反应.方法 60例突发性聋患者按入院顺序随机分为对照组和观察组各30例,对照组采用......
Researches have been done on Musée des Beaux Arts in terms of its theme,other aspects are ignored and have not been tou......
Mutations in the GJB2 gene are the most frequently found mutations in patients with nonsyndromic hearing impairment. How......
Objective To construct a prokaryotic expression vector bearing fusion gene NT4-ADNF-9 for future studies on genetic ther......
Each component of the human ear performs a specific function in hearing.The actual process of sound transduction takes p......
The International Symposium of Deafness and Genetic Medicine (ISDGM), organized by Department of Otolaryngology-Head & N......
The genetic load for hereditary hearing impairment in Chinese population and its clinical implicatio
Objective To understand the genetic load in the Chinese population for improvement in diagnosis, prevention and rehabili......
AIM:To analyze the clinical manifestation of Alport syndrome,especially the ocular features. METHODS:The physical,ophtha......
Objective To establish a lymphocyte line capable of long survival and expressing human NT-3 to lay a foundation for futu......
Objective To study the audition and inner ear structure in a normal swine model.Methods Auditory brainstem responses(ABR......
Objective To study effects of Adenovirus -mediated Hath1 expression in guinea pig cochlea at one month after exposure to......
Objective To report a population-based survey on the prevalence,pathogenic factors and medical needs of ear diseases and......
Objective To evaluate the effect of different protocols of intratympanic dexamethasone injection in patients with unilat......
Objective To study concomitant symptoms and disease conditions in sudden deafness. Methods Clinical data of 418 cases of......
