Results 81 to 90 of about 808,804 (186)

Functional and Morphological characterization of NOD-SCID inner ear

open access: yes, 2013
OBJECTIVE. Sensorineural hearing impairment is a consequence of hair cells (HC) and/or spiral ganglion neurons loss. In mammals, HCs are unable to regenerate, so their loss cause irreversible damages.
ASTOLFI, LAURA   +6 more
core  

Histopathology of Inner Ear Malformations: Potential Pitfalls for Cochlear Implantation

open access: yes, 2019
Hypothesis: The presence of bony inner ear malformations may associate with a number of anatomical abnormalities affecting the middle ear structures. Those malformations may create pitfalls and complications for cochlear implantation.
Rafael da Costa Monsanto   +11 more
core   +1 more source

Impact of inner ear malformation and cochlear nerve deficiency on the development of auditory-language network in children with profound sensorineural hearing loss. [PDF]

open access: yesElife, 2023
Wang Y   +15 more
europepmc   +1 more source

Non conventional signal transmission at the mouse vestibular Type I hair cell - calyx synapse

open access: yes, 2018
Vestibular sensory epithelia of Amniotes contain two types of hair cells, Type I and Type II, which differ in electrophysiological properties and synaptic contacts. Type I hair cells alone express a low-voltage activated outward rectifying K+ conductance,
Sergio Masetto   +5 more
core  

Eps8 regulates cochlear and vestibular hair cell development

open access: yes, 2016
Deletion of Epidermal growth factor receptor pathway substrate 8 (Eps8), a gene involved in actin remodeling, causes deafness in mice. Cochlear inner hair cells from Eps8-knockout (KO) mice have abnormally short stereocilia and fail to acquire their ...
ZAMPINI, VALERIA   +8 more
core  

Otosclerosis associated with type B-1 inner ear malformation [PDF]

open access: yes, 2010
Malformations of bony inner ear are rare anomalies occurring in approximately 20% of patients with congenital sensorineural hearing loss. Conductive hearing loss is usually associated with abnormalities of the external and middle ear.
Dispenza F.   +3 more
core  

Inner Ear Malformations with Transitional Forms between Cochlear Hypoplasia and Common Cavity: Embryological Insights, Imaging Characteristics, and Cochlear Implantation Strategies

open access: yesJournal of Otology
ObjectivesTo investigate the imaging characteristics, surgical approaches, and outcomes of cochlear implantation (CI) in patients with special inner ear malformations (IEMs) that show transitional forms between cochlear hypoplasia (CH) and common cavity (
Shujin Xue   +6 more
doaj   +1 more source

CSF Otorhinorrhea Due to Inner Ear Malformation-A Case Report. [PDF]

open access: yesIndian J Otolaryngol Head Neck Surg, 2022
Gupta AK   +3 more
europepmc   +1 more source

Clinical portrait of cochlear implantation in patients with incomplete partition type-III malformation

open access: yesFrontiers in Pediatrics
ObjectiveTo investigate the clinical characteristics and postoperative speech development in children with incomplete partition type III (IPIII) cochlear malformation.MethodsA retrospective analysis was conducted on 6 patients (12 ears) diagnosed with ...
Peng Zhu   +4 more
doaj   +1 more source

Major Contribution of GREB1L Alterations to Severe Inner Ear Malformation Largely in a Non-mendelian Fashion. [PDF]

open access: yesClin Exp Otorhinolaryngol, 2022
Kim BJ   +7 more
europepmc   +1 more source

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