Results 221 to 230 of about 825,232 (363)

Dual AAV gene therapy achieves recovery of hearing and auditory processing in a DFNB16 mouse model

Clinical and Translational Medicine, Volume 16, Issue 1, January 2026.
DFNB16 is among the most prevalent forms of congenital deafness, caused by mutations in the Stereocilin gene. Although no treatment currently exists, gene therapy represents a promising curative approach. Here, we demonstrate that AAV‐mediated gene delivery in a DFNB16 mouse model restored both peripheral hearing and central auditory processing ...
Sepideh Iranfar, Sophie Bagur, Chloé Felgerolle, Maxence Cornille, Najate Benamer, Hélène Le Ribeuz, Marie Giorgi, Sara Jamali, Amel Saoudi, Marie‐José Lecomte, Vincent Michel, Brice Bathellier, Saaid Safieddine   +12 more
wiley   +1 more source

Silent Signals: Unveiling Cochlear Nerve Deficiency in a Child Through Imaging. [PDF]

Cureus
Khaladkar SM, Sharma O, Jain S, Varma A.
europepmc   +1 more source

Cochlear Nerve Action Potential Monitoring with the Microdissector in Vestibular Schwannoma Surgery

, 2009
Noritaka Aihara, Shingo Murakami, Nobuhiro Watanabe, Mariko Takahashi, Akira Inagaki, Motoki Tanikawa, Kazuo Yamada   +6 more
openalex   +2 more sources

Developmental Expression of Membrane Pumps and Ion Channels in Human Vestibular Endolymph Homeostasis

Developmental Neurobiology, Volume 86, Issue 1, January 2026.
ABSTRACT The expression patterns of key membrane pumps and ion channels involved in endolymph cycling have been studied in the rodent inner ear and the developing and adult human cochlea. However, little is known about their expression during the development of the human vestibular system.
Edward S. A. van Beelen, Wouter H. van der Valk, John C. M. J. de Groot, Peter Paul G. van Benthem, Heiko Locher   +4 more
wiley   +1 more source

[Issues of auditory implant in children with cochlear nerve deficiency]. [PDF]

Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi
Zhang Z, Chen J.
europepmc   +1 more source

Correlation of cochlear aperture stenosis with cochlear nerve deficiency in congenital unilateral hearing loss and prognostic relevance for cochlear implantation. [PDF]

Sci Rep, 2021
Orzan E, Pizzamiglio G, Gregori M, Marchi R, Torelli L, Muzzi E.   +5 more
europepmc   +1 more source

A Novel Frameshift Variant c.1023_1029del (p.Asp342ArgfsTer54) Leading to Extended Incorrect Protein C Termini in HOMER2 Causing Autosomal Dominant Nonsyndromic Hearing Loss

Journal of Clinical Laboratory Analysis, Volume 40, Issue 1, January 2026.
We identified a novel c.1023_1029del (p.Asp342ArgfsTer54) frameshift variant in the HOMER2 gene that causes ADNSHL in a Chinese family with progressive, post‐lingual sensorineural hearing loss. The c.1023_1029del variant deletes 7 nucleotides, leading to an extended incorrect protein C terminus and marks the sixth pathogenic (or likely pathogenic ...
Li‐Ting Peng, Wei‐Qian Wang, Sha‐Sha Huang, Min Liu, Su‐Yan Yang, Dong‐Yang Kang, Xiang Wang, Xue Gao, Yong‐Yi Yuan, Jin‐Cao Xu   +9 more
wiley   +1 more source

Manuscript title: Transtympanic hijab pin injury: A rare cause of delayed-onset facial and cochlear nerve palsy with rehabilitative challenges in resource-limited settings: A case report. [PDF]

Int J Surg Case Rep
Hasan B, Hamdan Z, Ali L.
europepmc   +1 more source

Cochlear Implantation in Refsum Disease with Facial Nerve Enlargement

, 2018
Mihaéla Horoi, Stelianos Kampouridis, Levent Sennaroğlu, Marie‐Paule Thill   +3 more
openalex   +1 more source

Comparison of Temporal Bone Parameters before Cochlear Implantation in Patients with and without Facial Nerve Stimulation [PDF]

, 2019
Venkatkrish M. Kasetty, Zachary Zimmerman, Sarah King, Mohammad Seyyedi   +3 more
openalex   +1 more source