Four Cases of Idiopathic Sudden Sensorineural Hearing Loss.
, 1998 Taisuke Kurokawa, Kaori Yamaura
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Predictors of Early and Long‐Term Sound Quality Ratings in Adult Cochlear Implant Recipients
The Laryngoscope, Volume 136, Issue 1, Page 411-419, January 2026.This longitudinal study of 339 adult cochlear implant recipients demonstrates that subjective sound quality ratings improve significantly during the first 6 months post‐activation before plateauing, with early outcomes predicted by electrode placement factors (closer modiolar distance and deeper insertion depth), pre‐operative sound quality, and word ...
Katelyn A. Berg +2 more
wiley +1 more source
COVID-19 Vaccine-Associated Sensorineural Hearing Loss and Tinnitus. [PDF]
CureusSzilágyi A +3 more
europepmc +1 more source
Two cases of steroid dependent sensorineural hearing loss.
, 1989 Hironobu Kurokawa +3 more
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Impact of Acute Versus Chronic Unilateral Hearing Loss on Head Movement in a Novel Binaural Task
The Laryngoscope, Volume 136, Issue 1, Page 434-442, January 2026.Individuals with single‐sided deafness (SSD) may develop adaptive listening strategies with head movement patterns to optimize monaural localization and speech‐in‐noise understanding. Granular understanding of adaptive behaviors may better inform rehabilitation for SSD.
Madison V. Epperson +4 more
wiley +1 more source
Efficacy of intratympanic methylprednisolone versus standard therapy in adult sudden sensorineural hearing loss. [PDF]
Front NeurolMeng XD, Li TT, Zhang BT.
europepmc +1 more source
Cerebral volume and diffusion MRI changes in children with sensorineural hearing loss
, 2020 Peter K. Moon +12 more
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Targeting Ferroptosis in Sensorineural Hearing Loss: A Mechanistic Review of Therapeutic Opportunities. [PDF]
Curr Issues Mol BiolLiu H +5 more
europepmc +1 more source
Brainstem Infarction with Acute Sensorineural Hearing Loss. A Case Report.
, 1998 Takashi Nasu +4 more
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A Novel Intronic Variant Causes Aberrant Splicing of PCDH15 in a Family With Usher Syndrome Type 1F
Molecular Genetics &Genomic Medicine, Volume 14, Issue 1, January 2026.Minigene splicing assays elucidated the pathogenicity of a novel intronic c.3717+5G>A mutation in the PCDH15 gene, which was identified in a family affected by Usher syndrome type 1F. The results demonstrated that the c.3717+5G>A mutation can lead to exon 27 skipping and retention of 51 bp at the 5′ end of intron 27, resulting in truncated or abnormal ...
Qifan Ma +3 more
wiley +1 more source