Effects of ambient acoustic noise on the auditory steady-state response thresholds in normally hearing adults [0.03%]
噪声对正常听力成人频率特异性的听觉稳态反应阈值的影响
Joseph Kei,Damian Smith,Salimon Joseph et al.
Joseph Kei et al.
The effect of noise on auditory steady-state response (ASSR) has not been systematically studied, despite the fact that ASSR thresholds are sometimes measured in noisy environments. This study examined the effects of noise (speech babble) o...
The effects of electrode montage on the amplitude of wave V in the auditory brainstem response to maximum length sequence stimuli [0.03%]
电极导联方式对最大长度序列刺激下听神经脑干反应波V幅度的影响
Ahmad Aidil Dzulkarnain,Wayne J Wilson,Andrew P Bradley et al.
Ahmad Aidil Dzulkarnain et al.
The use of maximum length sequence (MLS) stimuli to elicit an auditory brainstem response (ABR) has been limited, in part, by the observation that these stimuli reduce ABR wave amplitudes. This study recorded ABR waveforms from 14 normally ...
Facioscapulohumeral muscular dystrophy: a multicenter study on hearing function [0.03%]
面部肩胛肱型肌营养不良的听力功能多中心研究
Carlo P Trevisan,Ebe Pastorello,Mario Ermani et al.
Carlo P Trevisan et al.
Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant progressive myopathy, characteristically associated with a 4q35 deletion. In the unusual infantile-onset form of this degenerative disease, sensorineural hearing loss is...
Multicenter Study
Audiology & neuro-otology. 2008;13(1):1-6. DOI:10.1159/000107431 2008
M Sainz,J García-Valdecasas,M Garófano et al.
M Sainz et al.
Introduction: Constant histological changes in otosclerosis lead to progressive hearing loss which may end up in a profound hearing loss and then be treated by means of cochlear implants. These progressive changes could b...
When tinnitus loudness and annoyance are discrepant: audiological characteristics and psychological profile [0.03%]
耳鸣响度和烦恼不一致时的听力学特征及心理特征
Wolfgang Hiller,Gerhard Goebel
Wolfgang Hiller
This study evaluates sociodemographic and clinical characteristics of patients reporting discrepant levels of tinnitus loudness and annoyance. 4958 subjects recruited from a national tinnitus association completed a comprehensive screening ...
Evaluation of an independent prestin mouse model derived from the 129S1 strain [0.03%]
基于129S1品系的独立 prestin 小鼠模型的评估
M A Cheatham,J Zheng,K H Huynh et al.
M A Cheatham et al.
Studies using the prestin knockout mouse indicate that removal of the outer hair cell (OHC) motor protein is associated with loss of sensitivity, frequency selectivity and somatic electromotility. Here we provide data obtained from another ...
Activation in primary auditory cortex during silent lipreading is determined by sex [0.03%]
大脑初级听觉皮层在无声唇读时的激活受性别影响
Liesbet Ruytjens,Frans Albers,Pim van Dijk et al.
Liesbet Ruytjens et al.
Recent studies investigating whether the primary auditory cortex (PAC) is involved in silent lipreading gave inconsistent results. We used positron emission tomography to identify which areas in the temporal lobe process visible speech, wit...
An alternative diagnostic test for active Ménière's disease and cochlear hydrops using high-pass noise masked responses: the complex amplitude ratio [0.03%]
一种用于诊断梅尼埃病和耳蜗积水的替代检测方法：使用高通噪声掩蔽反应的复振幅比
Manuel Don,Betty Kwong,Chiemi Tanaka
Manuel Don
We [Don et al.: Otol Neurotol 2005;26:711-722] previously demonstrated that patients diagnosed with an active case of Ménière's disease could be distinguished from non-Ménière's normal-hearing subjects by a special auditory brainstem re...
The complexity of age-related hearing impairment: contributing environmental and genetic factors [0.03%]
老年性听力下降的复杂性：影响因素及其遗传机制分析
E Van Eyken,G Van Camp,L Van Laer
E Van Eyken
Age-related hearing impairment (ARHI) is the most common sensory impairment seen in the elderly. It is a complex disorder, with both environmental as well as genetic factors contributing to the impairment. The involvement of several environ...
Studies of otic capsule morphology and gene expression in the Mov13 mouse--an animal model of type I osteogenesis imperfecta [0.03%]
Mov13小鼠耳囊形态及基因表达的研究——一种I型成骨不全症动物模型研究
Konstantina M Stankovic,Arthur G Kristiansen,Argyro Bizaki et al.
Konstantina M Stankovic et al.
Type I osteogenesis imperfecta (OI) is a disorder of skeletal bones characterized by bone fragility and blue sclera, which can result from mutations in genes encoding for type I collagen--the COL1A1 and COL1A2 genes. Fifty percent of patien...