Hearing Loss, Sensorineural
"Hearing Loss, Sensorineural" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Hearing loss resulting from damage to the COCHLEA and the sensorineural elements which lie internally beyond the oval and round windows. These elements include the AUDITORY NERVE and its connections in the BRAINSTEM.
Below are MeSH descriptors whose meaning is more general than "Hearing Loss, Sensorineural".
Below are MeSH descriptors whose meaning is more specific than "Hearing Loss, Sensorineural".
This graph shows the total number of publications written about "Hearing Loss, Sensorineural" by people in this website by year, and whether "Hearing Loss, Sensorineural" was a major or minor topic of these publications.
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Below are the most recent publications written about "Hearing Loss, Sensorineural" by people in Profiles.
The expanding LARS2 phenotypic spectrum: HLASA, Perrault syndrome with leukodystrophy, and mitochondrial myopathy. Hum Mutat. 2020 08; 41(8):1425-1434.
Predictors of Hearing Aid Use in the Advanced Digital Era: An Investigation of Benefit, Satisfaction, and Self-Efficacy. J Am Acad Audiol. 2020 02; 31(2):87-95.
Effect of Reduced Audibility on Mini-Mental State Examination Scores. J Am Acad Audiol. 2019 Nov/Dec; 30(10):845-855.
Evaluating speech perception of the MAXUM middle ear implant versus speech perception under inserts. Laryngoscope. 2018 02; 128(2):456-460.
Reduced penetrance in a large Caucasian pedigree with Stickler syndrome. Ophthalmic Genet. 2017 Jan-Feb; 38(1):43-50.
Hearing Aid Benefit in Patients with Mild Sensorineural Hearing Loss: A Systematic Review. J Am Acad Audiol. 2016 04; 27(4):293-310.
Evaluation of wideband frequency responses and nonlinear frequency compression for children with cookie-bite audiometric configurations. J Am Acad Audiol. 2014 Nov-Dec; 25(10):1022-33.
Adult and near-adult height in patients with severe insulin-like growth factor-I deficiency after long-term therapy with recombinant human insulin-like growth factor-I. Horm Res Paediatr. 2013; 80(1):47-56.
Mutation in collagen II alpha 1 isoforms delineates Stickler and Wagner syndrome phenotypes. Mol Vis. 2013; 19:759-66.
Report of a young girl with MYH9 mutation and review of the literature. J Pediatr Hematol Oncol. 2012 Oct; 34(7):538-40.