Below are the most recent publications written about "Hearing Loss, Sensorineural" by people in Profiles.
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van der Ende SR, Meyers BS, Capasso JE, Sasongko M, Yonekawa Y, Pihlblad M, Huey J, Bedoukian EC, Krantz ID, Ngo MH, McMaster CR, Levin AV, Robitaille JM. Severe Familial Exudative Vitreoretinopathy, Congenital Hearing Loss, and Developmental Delay in a Child With Biallelic Variants in FZD4. JAMA Ophthalmol. 2022 09 01; 140(9):889-893.
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Magan T, Hammersmith KM, Viaene AN, Kumar P, Eagle RC, Milman T. Harboyan Syndrome: A Novel SLC4A11 Variant With Unique Genotype-Phenotype Correlation. Cornea. 2022 Aug 01; 41(8):1053-1057.
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Toscano M, Meenan K, Brennan M, White M, Cohn JE, Sataloff RT. Evaluation of stapes mobilization in the 21st century for conductive hearing loss in the otosclerotic ear. Am J Otolaryngol. 2021 Sep-Oct; 42(5):103059.
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Bluher A, Kawai K, Wang A, Stiles D, Licameli G. Obesity as a Possible Risk Factor for Pediatric Sensorineural Hearing Loss. Laryngoscope. 2021 06; 131(6):1416-1419.
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Cowan B, Oska S, Arianpour K, Svider PF, Bojrab D, Hong RS. A Systematic Review of Cochlear Implantation in Temporal Bone Fractures and the Significance of Otic Capsule Involvement. Otol Neurotol. 2020 12; 41(10):1309-1315.
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Lubner RJ, Barbarite E, Kondamuri N, Knoll RM, Ota HG, Lewis RM, Franck K, Remenschneider AK, Kozin ED. Hearing Vital Signs: Mobile Audiometry in the Emergency Department for Evaluation of Sudden Hearing Loss. Otolaryngol Head Neck Surg. 2020 11; 163(5):1025-1028.
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Jackson OA, Kaye AE, Lee A, Minugh-Purvis N, Cohen MA, Solot CB, McDonald-McGinn D, Jawad AF, Zackai EH, Kirschner RE. Orofacial Manifestations of Stickler Syndrome: An Analysis of Speech Outcome and Facial Growth After Cleft Palate Repair. Ann Plast Surg. 2020 06; 84(6):665-671.
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Masood MM, Farquhar DR, Brown KD, Pillsbury HC, King ER, O'Connell BP. Hearing Preservation and Speech Outcomes After Cochlear Implantation in Meniere's Disease. Laryngoscope. 2020 12; 130(12):2874-2878.
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Roshal DA, Dunn JP, Xu D. A Woman in Her 40s With Transient Neurological Symptoms, Migraine Headaches, and Hearing Loss. JAMA Neurol. 2019 Apr 01; 76(4):504-505.
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Williams KB, Brigatti KW, Puffenberger EG, Gonzaga-Jauregui C, Griffin LB, Martinez ED, Wenger OK, Yoder MA, Kandula VVR, Fox MD, Demczko MM, Poskitt L, Furuya KN, Reid JG, Overton JD, Baras A, Miles L, Radhakrishnan K, Carson VJ, Antonellis A, Jinks RN, Strauss KA. Homozygosity for a mutation affecting the catalytic domain of tyrosyl-tRNA synthetase (YARS) causes multisystem disease. Hum Mol Genet. 2019 02 15; 28(4):525-538.