Results 241 to 250 of about 54,480 (306)

Human versus AI in audiological practice: A comparative evaluation of ChatGPT and physician treatment decisions in idiopathic sudden sensorineural hearing loss. [PDF]

PLoS One
Caragli V, Pellegrino M, Pingani L, Galeazzi GM, Soloperto D, Genovese E, de Filippis C, Marioni G, Franz L.   +8 more
europepmc   +1 more source

Association of a Homozygous TYMP c.131G>C Variant With MNGIE in a Chinese Pedigree: Insights From Genetic Analysis and Computational Modeling

Molecular Genetics &Genomic Medicine, Volume 14, Issue 6, June 2026.
Researcher highlight: Extending beyond the recently reported compound heterozygous case, we report the same TYMP c.131G>C variant in a homozygous configuration, delivering key genetic evidence for its standalone pathogenicity in MNGIE. ABSTRACT Background Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is an autosomal recessive disorder ...
Ling Li, Xiu Chen, Hua Li, Kai Guo, Ting Zhang, Mingyi Ma, Songhua Zhao   +6 more
wiley   +1 more source

Apple Hearing Test Feature for the AirPods Pro 2: Accuracy, Reliability, and Time‐Efficiency

Otolaryngology–Head and Neck Surgery, Volume 174, Issue 6, Page 1484-1493, June 2026.
Abstract Objective To evaluate the accuracy, test‐retest reliability, and time‐efficiency of Apple's Hearing Test Feature (HTF) compared to reference standard pure‐tone audiometry (PTA). Study Design Cross‐sectional validation study. Setting Single‐center study at a university clinic. PTA was performed in a sound‐treated booth.
Megan Kruger, Vinaya Manchaiah, De Wet Swanepoel   +2 more
wiley   +1 more source

Impact of hyperbaric oxygen as initial treatment on idiopathic sudden sensorineural hearing loss prognosis: a propensity scores matching analysis. [PDF]

Braz J Otorhinolaryngol
Xie S, Hong W, Huang L, Hong Y.
europepmc   +1 more source

Functional reassessment of extended splice region variants in MYO7A with hearing loss and Usher syndrome

The Journal of Pathology, Volume 269, Issue 2, Page 222-231, June 2026.
Abstract MYO7A is a causal gene, underlying Usher syndrome type 1B (USH1B) and both autosomal recessive (DFNB2) and dominant (DFNA11) non‐syndromic hearing loss. Despite the large number of reported MYO7A variants (over 2,200), variants located in an extended splice region remain difficult to interpret and are often classified as variants of uncertain ...
Tao Shi, Yu Huang, Xiaohuan Su, Lisheng Yu, Yixin Zhao, Jing Cheng   +5 more
wiley   +1 more source

Cochlear Homeostasis in Sensorineural Hearing Loss: Mechanisms, Implications, and Therapeutic Prospects. [PDF]

Int J Mol Sci
Vlajkovic SM, Suzuki-Kerr H, Nayagam BA.
europepmc   +1 more source

Prenatal Tympanic Ring Anomaly Without Microtia: A Subtle Clue Toward Severe Early‐Onset Monogenic Disorders

Prenatal Diagnosis, Volume 46, Issue 7, Page 1096-1103, June 2026.
ABSTRACT Objective To investigate the genetic etiologies and clinical significance of fetal tympanic ring abnormalities detected during second‐trimester ultrasound in the absence of microtia. Method Between November 2019 and June 2024, we examined the fetal tympanic rings of 10,277 unselected pregnant women during the 20–22 weeks of morphology ...
Yung Hang Lam, Mengmeng Shi, Zirui Dong, Kwong Wai Choy, Tak Yeung Leung, Ye Cao   +5 more
wiley   +1 more source

Reversible sensorineural hearing loss linked to chronic allergic rhinitis. [PDF]

J Allergy Clin Immunol Glob
Ajeti R, Ajeti A, Bilal N, Kaya İ.
europepmc   +1 more source

Issue Information

Eye &ENT Research, Volume 3, Issue 2, Page 41-44, June 2026.
No abstract is available for this article.
wiley   +1 more source

Impact of Smart Hearing Aid Technology on Self-Esteem in Patients with Sensorineural Hearing Loss: A Cross-Sectional Multivariate Study. [PDF]

Healthcare (Basel)
Padurean LL, Frandes M, Stefanescu HE, Muntean C, Horhat ID.   +4 more
europepmc   +1 more source