Results 81 to 90 of about 5,722 (237)
The present study was to investigate the dynamics of endolymphatic hydrops (EH) and hearing function, and explore whether the hearing loss is caused by EH alone and whether the hearing function can be modulated by changes in the EH.
Anquan Peng+7 more
doaj +1 more source
Endolymphatic Duct Blockage and Anatomical Variations Management
Endolymphatic duct blockage technique should be dictated by a precise anatomical understanding and surgical adaptation. This article focuses on the surgical approaches and anatomical variations of the endolymphatic sac during the transmastoid route, which varies with the size of the duct within the petrous bone and its accessibility.
Stéphane Gargula+5 more
wiley +1 more source
Tumors in von Hippel–Lindau Syndrome: From Head to Toe—Comprehensive State-of-the-Art Review [PDF]
Von Hippel–Lindau syndrome (VHL) is an autosomal-dominant hereditary tumor disease that arises owing to germline mutations in the VHL gene, located on the short arm of chromosome 3.
Bhalla, Sanjeev+6 more
core +1 more source
This study investigates the association between MASLD and sudden sensorineural hearing loss (SSNHL) among older adults in Korea. Our findings suggest a potential link between MASLD and an increased risk of SSNHL, emphasizing the need for further research and clinical awareness of this association. ABSTRACT Objectives This study examined the association
Eun Seok Kang+7 more
wiley +1 more source
MR imaging of endolymphatic hydrops in Ménière’s disease: feasibility at 1.5 T
Background Ménière’s disease is a chronic condition of the inner ear that causes vertigo, tinnitus and hearing loss. Its diagnosis relies on clinical criteria that are subjective and pure-tone audiometry results that are not specific.
Amine Ben Lakhal+4 more
doaj +1 more source
X‐Linked Hypophosphataemia and Burosumab: A Systemic Disease With a New Treatment
ABSTRACT X linked hypophosphataemia (XLH) is a systemic, chronic condition that significantly impairs quality of life. In XLH, a phosphate regulating endopeptidase homologue X‐linked (PHEX) gene mutation leads to excess fibroblast growth factor 23 (FGF23), causing hypophosphataemia and subsequent rickets, lower limb deformity, pain and other sequelae ...
Jessica L. Sandy+5 more
wiley +1 more source
Endolymphatic Hydrops: Pathophysiology and Experimental Models [PDF]
It is well established that endolymphatic hydrops plays a role in Ménière disease, even though the precise role is not fully understood and the presence of hydrops in the ear does not always result in symptoms of the disease. It nevertheless follows that a scientific understanding of how hydrops arises, how it affects the function of the ear, and how ...
Stefan K. Plontke, Alec N. Salt
openaire +3 more sources
ABSTRACT Objective To investigate the clinical characteristics and prognostic factors influencing treatment outcomes in pediatric sudden sensorineural hearing loss (PSSNHL). Methods A retrospective analysis was conducted on 63 children (64 ears) diagnosed with PSSNHL from January 2013 to December 2023.
Ranshi Zhao, Maoling Huang, Cheng Zhong
wiley +1 more source
Incorporating Vestibular Evoked Myogenic Potential (VEMP) assessment into our clinical practice [PDF]
Vestibular Evoked Myogenic Potentials (VEMPs) are short-latency electromyographic responses evoked by intense acoustic stimuli. They are measured in the ipsilateral, tonically-contracted sternocleidomastoid (SCM) muscle.
Jackson, Jacquelyn
core
Cochlear implantation : experimental and clinical studies [PDF]
Cochlear implantation makes hearing restoration possible in patients with severe to profound hearing loss. However, patients with residual hearing, where a cochlear implant may be combined with acoustic stimulation, and children with malformed cochleae ...
Smeds, Henrik
core +1 more source