Results 101 to 110 of about 6,888 (237)

Development of the occipitopetrosal junctions: A histological study using human fetuses

open access: yesThe Anatomical Record, Volume 309, Issue 2, Page 333-345, February 2026.
Abstract The temporal bone petrosa is connected to the occipital bone at two sites: one junction with the basilar part (medial junction) and another with the lateral part (lateral junction). Using histological specimens from 45 human fetuses (approximately 7–39 weeks of gestational age or GA), we aimed to describe possible changes in histology and ...
Ai Hirano‐Kawamoto   +6 more
wiley   +1 more source

Feline vestibular disorders. Part II: diagnostic approach and differential diagnosis. [PDF]

open access: yes, 1999
Results of a neurological examination usually permit localisation of a vestibular disorder to either the central or peripheral parts of the vestibular system. Many different disorders located in the same part of the vestibular system will produce similar
LeCouteur, RA, Vernau, KM
core  

Intraoperative Neurophysiological Monitoring for Endoscopic Endonasal Approaches to the Skull Base: A Technical Guide. [PDF]

open access: yes, 2016
Intraoperative neurophysiological monitoring during endoscopic, endonasal approaches to the skull base is both feasible and safe. Numerous reports have recently emerged from the literature evaluating the efficacy of different neuromonitoring tests during
Doan, Adam T.   +6 more
core   +3 more sources

Sensorineural Hearing Loss: What Lies Beneath? Neurovascular Conflict Secondary to a Dural Arteriovenous Malformation

open access: yesPhilippine Journal of Otolaryngology Head and Neck Surgery, 2014
This middle-aged gentleman with no previous medical history presented to the local ENT outpatient clinic complaining of right-sided hearing loss.  No history of trauma or previous head and neck surgery was elicited.
Ian C. Bickle
doaj   +1 more source

Dysphonia As an Uncommon Presentation of Pontocerebellar Choroid Plexus Papilloma

open access: yesActa Clinica Croatica, 2015
A case is presented of a patient with dysphonia, hearing loss and ataxia due to vestibulocochlear and vagal nerve compression by choroid plexus papilloma in the cerebellopontine angle.
Krešimir Rotim   +4 more
doaj  

Runx3 is required for the specification of TrkC-expressing mechanoreceptive trigeminal ganglion neurons [PDF]

open access: yes, 2010
Sensory neurons project axons to specific peripheral and central targets according to their sensory modality. Runx3 is crucially involved in proprioceptive dorsal root ganglion neuron development.
Ito Yoshiaki   +7 more
core   +1 more source

Comparison of Diffusion-Weighted MRI Reconstruction Methods for Visualization of Cranial Nerves in Posterior Fossa Surgery

open access: yesFrontiers in Neuroscience, 2017
Diffusion-weighted imaging (DWI)-based tractography has gained increasing popularity as a method for detailed visualization of white matter (WM) tracts.
Brendan Behan   +12 more
doaj   +1 more source

Association between hearing loss and vestibular disorders : a review of the interference of hearing in the balance [PDF]

open access: yes, 2015
Dizziness is very prevalent and makes a great impact on people’s life. Because of anatomical and functional similarities of hearing and vestibular systems, it is noted that there is a big relation between hearing loss and vestibular disorders.
Sampaio, André Luiz Lopes   +2 more
core   +1 more source

Bilateral Vestibulopathy in Superficial Siderosis

open access: yesFrontiers in Neurology, 2018
Background: Superficial siderosis (SS) is a rare condition in which hemosiderin, an iron storage complex, is deposited in neural tissues because of recurrent subarachnoid bleeding.
Sang-Yeon Lee   +5 more
doaj   +1 more source

Prenatal diagnosis and follow-up of a case of branchio-oto-renal syndrome displays renal growth impairment after the second trimester [PDF]

open access: yes, 2015
Branchio-oto-renal syndrome combines branchial arch defects, hearing impairment and renal malformations or hypoplasia. Due to the high phenotypic variability, prenatal diagnosis has a limited prognostic value in mutation-positive cases.
Bertucci, Emma   +5 more
core   +1 more source

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