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.
| Descriptor ID |
D006319
|
| MeSH Number(s) |
C09.218.458.341.887 C10.597.751.418.341.887 C23.888.592.763.393.341.887
|
| Concept/Terms |
|
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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1991 | 0 | 1 | 1 |
| 2001 | 1 | 0 | 1 |
| 2002 | 1 | 0 | 1 |
| 2008 | 1 | 0 | 1 |
| 2009 | 0 | 1 | 1 |
| 2010 | 0 | 1 | 1 |
| 2011 | 2 | 0 | 2 |
| 2012 | 1 | 1 | 2 |
| 2013 | 2 | 0 | 2 |
| 2014 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2017 | 2 | 0 | 2 |
| 2019 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hearing Loss, Sensorineural" by people in Profiles.
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Sarmadi A, Nasrniya S, Soleimani Farsani M, Narrei S, Nouri Z, Sepehrnejad M, Nilforoush MH, Abtahi H, Tabatabaiefar MA. A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family. BMC Med Genet. 2020 06 09; 21(1):127.
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Gaeta L, Azzarello J, Baldwin J, Ciro CA, Hudson MA, Johnson CE, John AB. Effect of Reduced Audibility on Mini-Mental State Examination Scores. J Am Acad Audiol. 2019 Nov/Dec; 30(10):845-855.
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Dyer RK, Spearman M, Spearman B, McCraney A. Evaluating speech perception of the MAXUM middle ear implant versus speech perception under inserts. Laryngoscope. 2018 02; 128(2):456-460.
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Tompson SW, Johnson C, Abbott D, Bakall B, Soler V, Yanovitch TL, Whisenhunt KN, Klemm T, Rozen S, Stone EM, Johnson M, Young TL. Reduced penetrance in a large Caucasian pedigree with Stickler syndrome. Ophthalmic Genet. 2017 Jan-Feb; 38(1):43-50.
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Johnson CE, Danhauer JL, Ellis BB, Jilla AM. Hearing Aid Benefit in Patients with Mild Sensorineural Hearing Loss: A Systematic Review. J Am Acad Audiol. 2016 04; 27(4):293-310.
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John A, Wolfe J, Scollie S, Schafer E, Hudson M, Woods W, Wheeler J, Hudgens K, Neumann S. 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.
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Backeljauw PF, Kuntze J, Frane J, Calikoglu AS, Chernausek SD. 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.
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Tran-Viet KN, Soler V, Quiette V, Powell C, Yanovitch T, Metlapally R, Luo X, Katsanis N, Nading E, Young TL. Mutation in collagen II alpha 1 isoforms delineates Stickler and Wagner syndrome phenotypes. Mol Vis. 2013; 19:759-66.
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Landi D, Lockhart E, Miller SE, Datto M, Rehder C, Kanaly A, Thornburg CD. Report of a young girl with MYH9 mutation and review of the literature. J Pediatr Hematol Oncol. 2012 Oct; 34(7):538-40.
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John AB, Hall JW, Kreisman BM. Effects of advancing age and hearing loss on gaps-in-noise test performance. Am J Audiol. 2012 Dec; 21(2):242-50.