Results 221 to 230 of about 172,130 (301)

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

Heimler Syndrome Caused by Novel <i>PEX6</i> Variants: Clinical and Genetic Characterization in a Saudi Cohort. [PDF]

Genes (Basel)
AlMoallem B.
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

Feasibility of Minimally Invasive Robot‐Assisted Retrofacial Access to the Stapedius Muscle for Applications in Objective Cochlear Implant Fitting: A Cadaveric Study

The International Journal of Medical Robotics and Computer Assisted Surgery, Volume 22, Issue 3, June 2026.
ABSTRACT Background Accurate setting of maximum comfort levels (MCL) during cochlear implant (CI) fitting is essential but subjective, especially in non‐cooperative patients. The stapedius reflex (SR) correlates with the MCL and offers an objective measure.
Dirk Arnold, Francesca Maule, Pablo Galeazzi, Mohannad Al‐Qubaj, Orlando Guntinas‐Lichius   +4 more
wiley   +1 more source

Early Auditory Stimulation, Not Device Type: Comparable Cortical Maturation in Children Using Cochlear Implants or Hearing Aids. [PDF]

Children (Basel)
Tumuklu K, Gunsoy B.
europepmc   +1 more source

Noise‐Induced Hearing Loss: From Pathological Mechanisms to Therapeutic Interventions

Sensory Neuroscience, Volume 2, Issue 2, June 2026.
ABSTRACT Noise‐induced hearing loss (NIHL), a significant non‐genetic form of hearing impairment, is primarily managed through the use of hearing aids and cochlear implants. However, the fundamental pathological mechanisms underlying NIHL remain inadequately addressed.
Shiqi Huang, Yu Xiao, Jiaxin Liu, Wen Jiang, Weiwei Shi, Hanbing Zhang, Xiaolong Fu, Yunhao Wu   +7 more
wiley   +1 more source

Latest clinical evidence and strategies for endoscopic intratympanic steroid injection in the treatment of sudden sensorineural hearing loss. [PDF]

Am J Transl Res
Xu DD.
europepmc   +1 more source

The Audiological Aspect of Beckwith-Wiedemann Syndrome: A Systematic Review. [PDF]

Genes (Basel)
Parretta S, Pellegrino M, Luppi L, Braglia E, Genovese E, Soloperto D.   +5 more
europepmc   +1 more source

Recurrent abdominal pain as a leading symptom for branchio-oto-renal syndrome: a case report. [PDF]

J Med Case Rep
Senjab A, Al Ayoubi O, Tannous G, Alsharef Y.   +3 more
europepmc   +1 more source

Correction to “Advances in the Treatment of Sensorineural Hearing Loss: From Traditional Therapies to Stem Cell and Gene Therapies”

Advanced Sensor Research, Volume 5, Issue 6, June 2026.
wiley   +1 more source