DEAFNESS

作品数:196被引量:560H指数:11
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相关领域:医药卫生更多>>
相关作者:韩德民戴朴吴皓王秋菊刘博更多>>
相关机构:首都医科大学中国人民解放军总医院武汉大学成都中医药大学更多>>
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In vivo consequences of varying degrees of OTOA alteration elucidated using knock-in mouse models and pseudogene contamination-free long-read sequencing
《Genes & Diseases》2025年第3期88-92,共5页Ju Ang Kim Bong Jik Kim Chung Lee Go Hun Seo Hane Lee Jin Hee Han Ava Niazi Joosang Park Byung Yoon Choi Sungjin Park 
supported by the National Research Foundation of Korea(NRF)grant funded by the Korean government(MSIT)(No.2021R1C1C1007980 to B.J.K.);Chungnam National University Sejong Hospital Research Fund,2022,and Chungnam National University(to B.J.K.);supported by the Basic Science Research Program through the NRF,funded by the Ministry of Education(No.2021R1A2C2092038 to B.Y.C.);Bio Core Facility Center program(No.NRF-2022M3A9G1014007 to B.Y.C.);the Basic Research Laboratory program through the NRF,funded by the Ministry of Education(No.RS-2023-0021971031482092640001 to B.Y.C.);the Technology Innovation Program(No.K_G012002572001 to B.Y.C.)funded By the Ministry of Trade,Industry&Energy(MOTIE,Korea);funded by SNUBH(Seoul National University Bundang Hospital)intramural research fund(No.13-2022-0010,02-2017-0060,16-2023-0002,13-2023-0002,16-2022-0005,13-2024-0004,and 13-2017-0013 to B.Y.C.);supported by the National Institute on Deafness and Other Communication Disorders(NIDCD);part of the US National Institutes of Health(No.R01DC018814 to S.P.).
Otoancorin(OTOA)is a glycosylphosphatidylinositol(GPI)-anchored protein mediating the attachment of the tectorial membrane(TM)to the spiral limbus(SL)in the inner ear.Homozygous or compound heterozygous mutations in O...
关键词:vivo consequences glycosylphosphatidylinositol anchored protein autosomal recessive deafness dfnb we tectorial membrane tectorial membrane tm pseudogene contamination free long read sequencing knock mouse models sensorineural hearing lossidentifying 
Developing a novel assistive technology,empowering the deaf to speak,using visual feedback.
《Journal of Otology》2025年第1期12-19,共8页Singh S Nagarajan K Chachan R Pandey P Vijayalakshmi P Verma N Singh A 
Background:Profoundly deaf children beyond 5 years of age and deaf adults with no prior access to hearing have limited options to learn oral speech.They rely mainly on sign language for communication.This is because,i...
关键词:DEAFNESS sign language cochlear implants speech to text deaf rehabilitation deaf speech 
激素不同给药途径治疗突发性聋疗效观察
《中国耳鼻咽喉头颈外科》2024年第11期742-744,共3页张晓红 鄢胜刚 高宇阳 
2024年浙江省中医药科技计划项目(2024ZF163)。
目的观察激素不同给药途径治疗突发性聋的疗效。方法回顾性分析海宁市中医院2021年4月~2024年4月间90例(90耳)突发性聋患者的病历资料,根据糖皮质激素用药方案分为静脉注射组26例(26耳)、鼓室注射组31例(31耳)、耳后注射组33例(33耳),...
关键词:耳聋(Deafness) 糖皮质激素类(Glucocorticoids) 投药途径(Drug Administration Routes) 注射 静脉内(Injections Intravenous) 鼓室注射(injection of tympanic cavity) 耳后注射(postauricular injection) 
The effect of right versus left long-term single-sided deafness on sound source localization
《Journal of Otology》2024年第3期158-162,共5页Qingqing Xia Shuoshuo Kang Qian Wang Mengdi Hong Aiting Chen Wei Chen Fei Ji Jianan Li Shiming Yang 
supported by the National Key Research and Development Project of China(2020YFC20052003 to S.M.Yang);Key International(Regional)Joint Research Program of National Natural Science Foundation of China(NSFC#81820108009 to S.M.Yang);National Natural Science Foundation of China(NSFC#82000976 to J.N.Li).
Purpose: To analyze the effect of right versus left long-term single-sided deafness(SSD) on sound source localization(SSL), discuss the necessity of intervention and treatment for SSD patients, and analyze the therape...
关键词:Single-sided deafness Cochlear implantation Sound source localization Treatment 
Thiamine responsive megaloblastic Anemia and deafness: A rare case of Roger’s syndrome with successful hearing rehabilitation by cochlear implantation
《Journal of Otology》2024年第3期163-165,共3页Hetal Marfatia Anoushka Sahai Kartik Narkhede Monankita Sharma 
Thiamine responsive megaloblastic anemia(TRMA),also known as Roger’s syndrome,is an exceptionally rare autosomal recessive disorder stemming from mutations in the SLC19A2 gene responsible for encoding a thiamine carr...
关键词:Roger’s syndrome Diabetic ketoacidosis Megaloblastic anemia Hearing loss Cochlear implant 
Abnormal Innervation,Demyelination,and Degeneration of Spiral Ganglion Neurons as Well as Disruption of Heminodes are Involved in the Onset of Deafness in Cx26 Null Mice
《Neuroscience Bulletin》2024年第8期1093-1103,共11页Yue Qiu Le Xie Xiaohui Wang Kai Xu Xue Bai Sen Chen Yu Sun 
supported by the National Key Research and Development Program of China(2021YFF0702303);the National Natural Science Foundation of China(82301324,82301323,and 82071058).
GJB2 gene mutations are the most common causes of autosomal recessive non-syndromic hereditary deafness.For individuals suffering from severe to profound GJB2-related deafness,cochlear implants have emerged as the sol...
关键词:Spiral ganglion neurons GJB2 Heminode Hearing loss 
Unveiling a novel GJB2 dominant K22T mutation in a Chinese family with hearing loss
《Acta Biochimica et Biophysica Sinica》2024年第6期945-951,共7页Haiting Ji Yilai Shu Huawei Li 
supported by the grants from the National Natural Science Foundation of China(Nos.81600816 and 82192860);the Original Scientific Research Supporting Program of Fudan University,Shanghai Municipal Key Clinical Specialty(No.shslczdzk00801);the Shanghai Science and Technology Committee(Shanghai Clinical Medical Research Center for Otorhinolaryngology)(No.20MC1920200).
Hearing loss constitutes one of the most prevalent conditions within the field of otolaryngology.Recent investigations have revealed that mutations in deafness-associated genes,including point mutations and variations...
关键词:DEAFNESS point mutations GJB2 next-generation sequencing 
Cultural conceptulisations in Elijah Akintunde's Yoruba ballad gospel song Jjo Odi‘Dance of the Deaf’
《Language and Semiotic Studies》2023年第3期313-332,共20页Rotimi Taiwo Mayowa Fawunmi Ajibola Ogundare 
What kind of actions or reactions can sudden good news elicit in the experiencer?How can these actions/reactions be cognitively interpreted by others?Is there a nexus between social realities and the gospel?Using thes...
关键词:conceptual categories conceptualisation cultural linguistics dance DEAFNESS METAPHOR SCHEMAS 
淮北市听力筛查异常婴幼儿耳聋易感基因筛查特点分析被引量:2
《中国耳鼻咽喉头颈外科》2023年第7期461-463,共3页张玲 钟辉 化金金 
目的 分析淮北市听力筛查异常婴幼儿耳聋易感基因的特点,为婴幼儿耳聋防治工作的开展提供参考。方法选取2018年4月~2023年1月在淮北市妇幼保健院进行听力筛查的新生儿为研究对象,采用自动听性脑干诱发电位反应(AABR)和诊断性畸变产物耳...
关键词:耳聋(Deafness) 婴儿(Infant) 听力损失(Hearing Loss) 新生儿筛查(Neonatal Screening) 易感基因(susceptible gene) 
Various aspects of hearing loss in newborns:A narrative review被引量:1
《World Journal of Clinical Pediatrics》2023年第3期86-96,共11页Raid M Al-Ani 
Hearing loss is considered the most common birth defect.The estimated prevalence of moderate and severe hearing loss in a normal newborn is 0.1%-0.3%,while the prevalence is 2%-4%in newborns admitted to the newborn in...
关键词:NEWBORNS Hearing loss DEAFNESS SENSORINEURAL 
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