Below are the most recent publications written about "Hearing Loss, Sensorineural" by people in Profiles.
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Riley LG, Rudinger-Thirion J, Frugier M, Wilson M, Luig M, Alahakoon TI, Nixon CY, Kirk EP, Roscioli T, Lunke S, Stark Z, Wierenga KJ, Palle S, Walsh M, Higgs E, Arbuckle S, Thirukeswaran S, Compton AG, Thorburn DR, Christodoulou J. The expanding LARS2 phenotypic spectrum: HLASA, Perrault syndrome with leukodystrophy, and mitochondrial myopathy. Hum Mutat. 2020 08; 41(8):1425-1434.
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Jilla AM, Johnson CE, Danhauer JL, Anderson M, Smith JN, Sullivan JC, Sanchez KR. 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.
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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.