Predictors of Dizziness and Hearing Disorders in People with Long COVID. [PDF]
Medicina (Kaunas), 2023 Obeidat FS, Alghwiri AA, Whitney SL.
europepmc +3 more sources
A case of Langerhans cell histiocytosis localized in the temporal bone, which presented as sudden sensorineural hearing loss: A case report and review of the literature [PDF]
SAGE Open Medical Case ReportsSudden sensorineural hearing loss is a condition marked by a rapid decline in hearing, defined as a decrease of 30 dB or more across three adjacent audiometric frequencies within 72 h.
Farzin Davoodi +5 more
doaj +2 more sources
Explainable AI-based clinical decision support system for hearing disorders. [PDF]
AMIA Jt Summits Transl Sci Proc, 2021 Tarnowska KA, Dispoto BC, Conragan J.
europepmc +2 more sources
Deep phenotyping to understand hearing and hearing disorders: Protocol for a feasibility study. [PDF]
PLoS OneSpriggs RV +6 more
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Hearing Threshold of Auditory Brainstem Response in Term Neonates with Hyperbilirubinemia [PDF]
Journal of Kerman University of Medical Sciences, 2021 Background:Neonatal jaundice is a common cause of premature neonatal hearing loss and is a major cause of childhood deafness, especially in developing countries.
Fatemeh Eghbalian +5 more
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MicroRNAs in Hearing Disorders: Their Regulation by Oxidative Stress, Inflammation and Antioxidants. [PDF]
Front Cell Neurosci, 2017 Prasad KN, Bondy SC.
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Improving the Level of Ear Health Literacy in Teenager: Policy Brief [PDF]
پژوهان, 2023 According to the World Health Organization, 360 million people worldwide have disabling hearing loss. Of these, 32 million people are hard hearing or deaf under the age of 15.
Homa Naderifar, Roya Najafi-Vosough
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Hearing Improvement in A/J Mice via the Mouse Nerve Growth Factor [PDF]
Clinical and Experimental Otorhinolaryngology, 2017 Objectives To investigate the otoprotective effects of mouse nerve growth factor (mNGF) in A/J mice. Methods The mice at postnatal day 7 (P7) were randomly separated into a mNGF treated group (mNGF group) and a distilled water (for injection) treated ...
Lixiang Gao +7 more
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A novel mutation in TRIOBP gene leading to congenital deafness in a Chinese family
BMC Medical Genetics, 2020 Background The autosomal recessive non-syndromic deafness DFNB28 is characterized by prelingual sensorineural hearing loss. The disease is related with mutations in TRIOBP (Trio- and F-actin-Binding Protein) gene, which has three transcripts referred to ...
Bingxin Zhou +6 more
doaj +1 more source
Stapedotomy Favorable Outcome on Osteosclerosis Patient's with High Pitch Tinnitus
Otorhinolaryngology and Facial Plastic Surgery, 2022 Background: Otosclerosis is a primary disease of the temporal bone and otic capsule with autosomal dominant transmission and variable expression. The exact pathogenesis and factors affecting tinnitus in otosclerosis patients are unknown. This study aims
Farhad Mokhtarinejad +2 more
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