Results 81 to 90 of about 4,323 (203)

"COCHLEAR IMPLANTATION IN PATIENTS WITH INNER EAR MALFORMATIONS" [PDF]

open access: yesActa Medica Iranica, 2004
Performing cochlear implantation in patients with inner ear malformation has always been a matter of dispute. This study was designed to analyze the operative findings,complications, and postoperative performance of patients with inner ear anomalies who ...
MH. Khalessi   +2 more
doaj   +1 more source

CT-Scans of Cochlear Implant Patients with Characteristics of Pendred Syndrome

open access: yesCellular Physiology and Biochemistry, 2013
Background: Sensorineural hearing loss (SNHL) in newborns is estimated with an incidence around 1:10,000 per year and is divided into syndromic and non-syndromic forms.
Sebastian Roesch   +3 more
doaj   +1 more source

Magnetic resonance imaging features of large endolymphatic sac compartments: audiological and clinical correlates [PDF]

open access: yes, 2017
Objectives: (1) To study the prevalence and characteristics of large endolymphatic sac internal compartments on thin-section T2- and T2*-weighted magnetic resonance imaging, and to relate these to other large endolymphatic sac magnetic resonance imaging ...
Connor, S E J.   +6 more
core  

AAVR Expression is Essential for AAV Vector Transduction in Sensory Hair Cells

open access: yesAdvanced Science, Volume 12, Issue 29, August 7, 2025.
Decreased sensitivity to AAV vector transduction in the outer hair cells (OHCs) of adult mice is primarily attributed to reduction of AAVR (Kiaa0319l; Au040320). Knockout of AAVR reduces AAV vector transduction efficiency in both inner hair cells (IHCs) and OHCs in neonatal mice.
Fan Wu   +8 more
wiley   +1 more source

Cochlear implantation of a child with Townes-Brocks Syndrome in Tanzania: a case report

open access: yesThe Egyptian Journal of Otolaryngology
Background Townes-Brocks Syndrome (TBS), an autosomal dominant disorder, is known to cause hearing loss amongst other expressions including anomalies that affect the external ear, hands, feet, anus, and kidneys.
Ali F. Jaffer   +4 more
doaj   +1 more source

Craniometaphyseal and craniodiaphyseal dysplasia, head and neck manifestations and management [PDF]

open access: yes, 2007
Craniometaphyseal and craniodiaphyseal dysplasia are rare genetic disorders of bone due to modelling errors of long bones and skull bones. These syndromes present with multiple ENT symptomatology from an early age.
Bailey, CM   +3 more
core   +1 more source

Contrast Agent Uptake in Endolymphatic Sac and Duct: Inverse Relation to Endolymphatic Hydrops

open access: yesThe Laryngoscope, Volume 135, Issue 8, Page 2914-2922, August 2025.
Question: Is there a disease‐specific abnormality of the endolymphatic sac and duct system (ES/ED) in delayed, contrast‐enhanced inner ear MRI in patients with Ménière's disease (MD) and vestibular migraine (VM) that correlates with the endolymphatic hydrops (ELH)?
Johannes Gerb   +6 more
wiley   +1 more source

Stimulation from Cochlear Implant Electrodes Assists with Recovery from Asymmetric Perceptual Tilt: Evidence from the Subjective Visual Vertical Test [PDF]

open access: yes, 2016
Vestibular end organ impairment is highly prevalent in children who have sensorineural hearing loss (SNHL) rehabilitated with cochlear implants (CIs). As a result, spatial perception is likely to be impacted in this population.
Blake C. Papsin   +5 more
core   +1 more source

Morphometric Analysis of the Internal Auditory Canal by Computed Tomography Imaging [PDF]

open access: yes, 2012
Background: Many clinical and experimental studies have been done to analyze the anatomical and functional aspects of the internal auditory canal (IAC) in human beings since there are great inter-individual variability and structural variations that may ...
Ajzen, Sergio   +5 more
core   +2 more sources

Mouse Models for Pendrin-Associated Loss of Cochlear and Vestibular Function

open access: yesCellular Physiology and Biochemistry, 2013
The human gene SLC26A4 and the mouse ortholog Slc26a4 code for the protein pendrin, which is an anion exchanger expressed in apical membranes of selected epithelia.
Philine Wangemann
doaj   +1 more source

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