Bilateral Posterior Semicircular Canal Dehiscence in the Setting of Hallermann-Streiff Syndrome [PDF]
John C. Goddard+2 more
openalex +1 more source
Abstract Ageing‐related sensory deteriorations are significantly associated with poor balance control among older individuals, resulting in a higher risk of falling in a dark environment. In particular, the proprioceptive system plays a critical role in maintaining balance.
Haoyu Xie+3 more
wiley +1 more source
Surgical access to separate branches of the cat vestibular nerve [PDF]
A posteroventral approach for access to separate branches of the cat vestibular nerve is presented which permits simultaneous surgical access to the ampullary and otolithic nerves.
Ayzikov, G. S., Radkevich, L. A.
core +1 more source
Canal switch and re-entry phenomenon in benign paroxysmal positional vertigo: difference between immediate and delayed occurrence [PDF]
Studio prospettico ideato per la valutazione delle differenze tra la conversione canalare o il rientro degli otoliti nei canali semicircolari successivo alle manovre terapeutiche nei pazienti affetti da VPPB.
Bennici E.+6 more
core
Nystagmus Discordance with 2‐Dimensional Videonystagmography in Posterior Semicircular Canal Benign Paroxysmal Positional Vertigo [PDF]
Crystal M. VanDerHeyden+2 more
openalex +1 more source
Abstract Purpose High‐resolution ex vivo diffusion‐weighted imaging (dMRI) with high b$$ b $$‐values presents significant challenges, including low signal‐to‐noise ratio (SNR), magnetic field perturbations, and temperature‐related measurement shifts.
Alina Müller+14 more
wiley +1 more source
Resolution of atypical posterior semicircular canal BPPV: evidence for putative short-arm location. [PDF]
Ludwig D, Schubert MC.
europepmc +1 more source
How we do it: locating the posterior semicircular canal in occlusion surgery for refractory benign paroxysmal positional vertigo: a cadaveric temporal bone study [PDF]
L. D. Hamilton+3 more
openalex +1 more source
Current preclinical studies of AAV‐mediated gene therapy explore different strategies based on the characteristics of inner ear diseases. For genetic hearing loss, approaches include the replacement of a “good gene,” removal of a “bad gene,” or direct correction of mutations through base editing.
Fan Wu+7 more
wiley +1 more source
Worth the Effort: Lessons for Discovery and Care From an Unusual Case of Gorlin Syndrome
ABSTRACT Gorlin‐Goltz Syndrome (GGS) is a rare autosomal dominant genetic disorder encompassing a diverse range of clinical manifestations, including congenital anomalies and predisposition to cancer. Pathogenic variants in PTCH1 and SUFU account for up to 79% and 6% of cases, respectively. Currently, an estimated 15%–27% of individuals with a clinical
V. Taliercio+13 more
wiley +1 more source