Results 61 to 70 of about 2,953,514 (241)
Molecular and Cellular Hallmarks of Age‐Related Vestibular Hair Cell Degeneration
This study utilizes single‐cell RNA‐seq transcriptomes, advanced imaging, and electrophysiology to examine universal and cell‐type‐specific aging signatures of vestibular hair cells. The study shows that impaired hair bundle function is a key driver of age‐related vestibular dysfunction.
Samadhi Kulasooriya +10 more
wiley +1 more source
On the vertigo due to static magnetic fields. [PDF]
Vertigo is sometimes experienced in and around MRI scanners. Mechanisms involving stimulation of the vestibular system by movement in magnetic fields or magnetic field spatial gradients have been proposed.
Antunes, Andre +14 more
core +2 more sources
Unilateral Hearing Loss Leading to a Diagnosis of Neurofibromatosis 2
Neurofibromatosis 2 (NF2) is a genetic condition characterized by multiple benign tumors of the nervous system. Bilateral vestibular schwannomas are considered pathognomonic for NF2 and often result in sensorineural hearing loss. We present the case of a
Terry M. Lou, Stacy Charat
doaj +1 more source
Using grilled lamb skewers as a model system, this work builds a multiscale coupling framework from oral processing to retronasal aroma perception, reveals dual‐kinetic release patterns and Electroencephalogram‐characterized central encoding features, and proposes an interpretable physics‐guided deep learning model validated by multiphysics simulation,
Che Shen +12 more
wiley +1 more source
The Effect of Vibrotactile Feedback on Healthy People and People with Vestibular Disorders during Dual-task Conditions [PDF]
Vibrotactile feedback (VTF) has been shown to improve balance performance in healthy people and people with vestibular disorders in a single-task experimental condition. However, typical balance activities occur in a multi-task environment.
Lin, Chia-Cheng
core
A Bilateral Vestibular Schwannoma is Not Always Related to Neurofibromatosis Type 2 [PDF]
: Bilateral vestibular schwannomas are commonly diagnosed in patients affected by neurofibromatosis type 2, a genetic disease caused by a heterozygous mutation in the gene region encoding neurofibromin-2.
Andi Abeshi +3 more
core +1 more source
IntroductionThe vestibular system is crucial for balance, spatial orientation, and gaze stabilization. Bilateral vestibulopathy (BV) severely impairs these functions, often co-occurring with severe to profound hearing loss.
David Lanthaler +9 more
doaj +1 more source
Cogan Syndrome: A Case Study and Review of the Literature
Cogan syndrome is an autoimmune disease characterized by vestibular symptoms, bilateral sensorineural hearing loss, and inflammatory ocular manifestations, which may be accompanied by systemic vasculitis.
Tasha Nasrollahi MD +3 more
doaj +1 more source
A root‐inspired microneedle array patch uses lattice‐based mechanical interlocking to unite rigid microneedles with a flexible substrate. The interlocked rigid–soft architecture improves interfacial bonding, supports stable adhesion on curved and wet tissues under dynamic motion, and provides a versatile platform for robust biointerfacing and future ...
Jongchan Lee +9 more
wiley +1 more source
TECTB Variants Reveal Tectorial Membrane Vulnerability in Dominant Non‐Syndromic Hearing Loss
TECTB is a non‐collagenous protein of the tectorial membrane – an extracellular matrix of the cochlea. This study identifies dominant missense variants in TECTB linked to human hereditary deafness in two unrelated families. Genetically engineered mice homozygous for one of the variants are profoundly deaf, whereas heterozygous mice have normal hearing ...
Evan B. Hale +23 more
wiley +1 more source

