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DisponibilitéExemplaires (1)
Cote Support Localisation Section Disponibilité International journal of audiology IJA. Vol. 56, n° 1-12 (January-December 2017) Périodique papier Ixelles Rez Consultation sur place uniquement
Exclu du prêtArticle
Objectives: Misplacement of the electrode array is associated with impaired speech perception in patients with cochlear implants (CIs). Translocation of the electrode array is the most common misplacement. When a CI is translocated, it crosses t[...]Article
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Carole E. Johnson, Auteur ; Anna Marie Jilla, Auteur ; Jeffrey L. Danhauer, Auteur |The number of people over 65 years of age is increasing, and many of those individuals will have sensorineural hearing loss in addition to other chronic health conditions. Future hearing health care providers need to be sensitive to the needs of[...]DisponibilitéExemplaires (1)
Cote Support Localisation Section Disponibilité Seminars in hearing. Vol. 39, n°1 (February 2018) Périodique papier Ixelles Rez Consultation sur place uniquement
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Objectives: The digits-in-noise test (DIN) is a popular self-test measure that has traditionally been used to screen for hearing loss by providing either a pass or refer result. Standard approaches either tested each ear monaurally or used a bin[...]Article
Objective: To examine the prevalence of hearing impairment in children with hypothyroidism, and to characterize clinical and subclinical hearing loss by examining cochlear function, auditory brainstem pathways, and integration of the auditory sy[...]Article
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Background In the 1950s, with monitored live voice testing, the vu meter time constant and the short durations and amplitude modulation characteristics of monosyllabic words necessitated the use of the carrier phrase amplitude to monitor (indir[...]DisponibilitéExemplaires (1)
Cote Support Localisation Section Disponibilité Journal of the American Academy of Audiology (JAAA). Vol.31, n°6 (Juin 2020) Périodique papier Ixelles Rez Consultation sur place uniquement
Exclu du prêtArticle
Lapproche génétique, basée sur létude des formes héréditaires de surdité, a été particulièrement efficace au cours des 25 dernières années pour révéler la physiologie moléculaire de la cochlée, lorgane sensoriel de laudition. En revanche, ce[...]Article
Evaluating the benefit of hearing aids with motion-based beamformer adaptation in a real-world setup
Solveig C. Voss ; M. Kathleen Pichora-Fuller ; Ieda Ishida ; April Pereira ; Julia Seiter ; Nadim El Guindi ; Volker Kuehnel ; Jinyu Qian |Objective Conventional directional hearing aid microphone technology may obstruct listening intentions when the talker and listener walk side by side. The purpose of the current study was to evaluate hearing aids that use a motion sensor to add[...]Article
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Damage to auditory hair cells is a key feature of sensorineural hearing loss due to aging, noise exposure, or ototoxic drugs. Though hair-cell loss is permanent in humans, research in bird species led to the discovery that analogous hair cells o[...]DisponibilitéExemplaires (1)
Cote Support Localisation Section Disponibilité Journal of the American Academy of Audiology. Vol. 32, n° 10 (November 2021) Périodique papier Ixelles Rez Consultation sur place uniquement
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Sébastien Janssens de Varebeke ; Ronald J. Pennings ; Vedat Topsakal ; Katrien Devroye ; Raymond van de Berg ; Erik Fransen ; Julie Moyaert ; Britt Bulen ; Celine Neesen ; Olivier Vanderveken ; Guy Van Camp ; Vincent Van Rompaey |DFNA9 is characterized by adult-onset progressive sensorineural hearing loss (SNHL) and vestibular impairment. More than 15 years ago, genotype-phenotype correlation studies estimated the initial age of hearing deterioration in the fourth to fif[...]Article
Sébastien Janssens de Varebeke ; Ronald J. Pennings ; Vedat Topsakal ; Katrien Devroye ; Raymond van de Berg ; Erik Fransen ; Julie Moyaert ; Britt Bulen ; Celine Neesen ; Olivier Vanderveken ; Guy Van Camp ; Vincent Van Rompaey |Introduction: DFNA9 is characterized by adult-onset hearing loss and evolution toward bilateral vestibulopathy (BVP). The genotype-phenotype correlation studies were conducted 15 years ago. However, their conclusions were mainly based on symptom[...]Article
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Ting-Ting Yen ; I-Chieh Chen ; Sudi Cho ; Ting-Gang Chang ; Kai-Hsiang Shih ; Men-Wei Hua ; Jui-Lin Li ; Chiann-Yi Hsu ; Tzu-Hung Hsiao ; Yi-Ming Chen |Background: Gap junction protein beta 2 (GJB2) p.V37I mutations are the most important hereditary cause of sensorineural hearing loss (SNHL) in Taiwan. Hearing outcomes are associated with hearing levels at baseline and the duration of follow-up[...]