Results 81 to 90 of about 808,804 (186)
Functional and Morphological characterization of NOD-SCID inner ear
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
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]
Wang Y +15 more
europepmc +1 more source
Non conventional signal transmission at the mouse vestibular Type I hair cell - calyx synapse
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
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]
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
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]
Gupta AK +3 more
europepmc +1 more source
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]
Kim BJ +7 more
europepmc +1 more source

