Results 61 to 70 of about 5,041 (178)

Regulation of Fn14 Receptor and NF-κB Underlies Inflammation in Meniere’s Disease

open access: yesFrontiers in Immunology, 2017
Meniere’s disease (MD) is a rare disorder characterized by episodic vertigo, sensorineural hearing loss, tinnitus, and aural fullness. It is associated with a fluid imbalance between the secretion of endolymph in the cochlear duct and its reabsorption ...
Lidia Frejo   +27 more
doaj   +1 more source

Navigating the Genetic Risk of Chemotherapy‐Induced Hearing Loss in the Stria Vascularis

open access: yesClinical Pharmacology &Therapeutics, Volume 119, Issue 4, Page 846-858, April 2026.
Cisplatin is a chemotherapy drug that causes permanent hearing loss by damaging a critical tissue lining the inner ear, called the stria vascularis (SV). Currently, the molecular mechanisms of SV damage are largely unknown and the incidence of ototoxicity in patients cannot be reliably predicted.
Tara Lazetic   +4 more
wiley   +1 more source

New non‐contrast MRI of endolymphatic hydrops in Ménière's disease considering inversion time

open access: yesLaryngoscope Investigative Otolaryngology
Objectives Three‐tesla MRI with gadolinium‐based contrast agents is important in diagnosing Ménière's disease. However, contrast agents cannot be used in some patients.
Masanori Ishii   +9 more
doaj   +1 more source

Genetic background of Meniere’s disease

open access: yesJournal of Medical Science, 2018
Meniere’s disease (MD) as an inner ear disorder including such symptoms as recurrent vertigo attacks, tinnitus, fluctuating or progressive sensorineural hearing loss. Its relatively frequent familial incidence implicates a genetic background.
Krzysztof Szyfter   +2 more
doaj   +1 more source

Lack of association between inner ear FLAIR suppression on MRI and laterality of clinical signs in feline idiopathic vestibular syndrome

open access: yesJournal of Feline Medicine and Surgery
Objectives The underlying aetiology of feline idiopathic vestibular syndrome (IVS) remains unclear. In humans, specific MRI sequences are used to demonstrate differences in endolymph composition between unaffected and affected inner ears.
Magdalena Putzer   +4 more
doaj   +1 more source

Ideas and perspectives: Mineralizing fluid control on foreign elements in biogenic CaCO3: insights from otoliths [PDF]

open access: yesBiogeosciences
The foreign element composition of calcium carbonate (CaCO3) biominerals from marine calcifying organisms leaving a sedimentary record has been used for decades to reconstruct various biogeochemical parameters.
A. Kekelou   +5 more
doaj   +1 more source

Three-Dimensional Computer Model of Benign Paroxysmal Positional Vertigo in the Semi-Circular Canal

open access: yesEAI Endorsed Transactions on Pervasive Health and Technology, 2018
Benign Paroxysmal Positional Vertigo (BPPV) is the most common vestibular disorder. In this paper we tried to investigate a model of the semi-circular canal (SCC) with parametrically defined dimension and full 3D three SCC from patient-specific 3D ...
Zarko Milosevic   +5 more
doaj   +1 more source

Guide the diagnosis and treatment of benign paroxysmal positional vertigo from the perspective of vestibular pathophysiology

open access: yesChinese Journal of Contemporary Neurology and Neurosurgery, 2019
This paper aims to explain the clinical features of benign paroxysmal positional vertigo (BPPV), the most common peripheral vertigo disease, from the view of vestibular pathophysiology.
Jian-hua ZHUANG
doaj  

Pressure relationship between perilymph and endolymph after the infusion of artificial endolymph into scala media.

open access: yesPractica Oto-Rhino-Laryngologica, 1990
The pressure difference between the perilymph and the endolymph following infusion of artificial endolymph into the endolymphatic space was studied in guinea pigs. The perilymphatic and the endolymphatic pressures were measured simultaneously with two sets of a servo-pulling system.
Takeuchi, Shunji   +2 more
openaire   +2 more sources

Complete omission of exon 21 from Slc12a2 transcripts in mice results in hearing loss

open access: yesScientific Reports
Hereditary hearing loss is highly heterogeneous. SLC12A2 is linked to autosomal dominant nonsyndromic hearing loss, DFNA78, with all the pathogenic variants affecting the exon 21.
Hideki Mutai   +8 more
doaj   +1 more source

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