Below are the most recent publications written about "Deafness" by people in Profiles.
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Chen R, Diaz-Miranda MA, Aref-Eshghi E, Hartman TR, Griffith C, Morrison JL, Wheeler PG, Torti E, Richard G, Kenna M, Dechene ET, Spinner NB, Bai R, Conlin LK, Krantz ID, Amr SS, Luo M. Characterization of a possible founder synonymous variant in TECTA in multiple individuals with autosomal recessive hearing loss. Hum Mutat. 2022 12; 43(12):1837-1843.
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Hwang MS, Britt CJ, Vila PM, Dang RP, Fleming SI, Patel AM, Paniello RC, Rich JT, Hanasono MM, Desai SC. Factors associated with skin graft take in fibula and radial forearm free flap donor sites. Am J Otolaryngol. 2020 Jul - Aug; 41(4):102536.
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Hoffman MF, Cejas I, Quittner AL. Health-Related Quality of Life Instruments for Children With Cochlear Implants: Development of Child and Parent-Proxy Measures. Ear Hear. 2019 May/Jun; 40(3):592-604.
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Lilly E, Bunick CG, Maley AM, Zhang S, Spraker MK, Theos AJ, Vivar KL, Seminario-Vidal L, Bennett AE, Sidbury R, Ogawa Y, Akiyama M, Binder B, Hadj-Rabia S, Morotti RA, Glusac EJ, Choate KA, Richard G, Milstone LM. More than keratitis, ichthyosis, and deafness: Multisystem effects of lethal GJB2 mutations. J Am Acad Dermatol. 2019 Mar; 80(3):617-625.
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Hoffman MF, Cejas I, Quittner AL. Comparisons of Longitudinal Trajectories of Social Competence: Parent Ratings of Children With Cochlear Implants Versus Hearing Peers. Otol Neurotol. 2016 Feb; 37(2):152-9.
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Hoffman MF, Quittner AL, Cejas I. Comparisons of social competence in young children with and without hearing loss: a dynamic systems framework. J Deaf Stud Deaf Educ. 2015 Apr; 20(2):115-24.
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Reesman JH, Day LA, Szymanski CA, Hughes-Wheatland R, Witkin GA, Kalback SR, Brice PJ. Review of intellectual assessment measures for children who are deaf or hard of hearing. Rehabil Psychol. 2014 Feb; 59(1):99-106.
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Mese G, Sellitto C, Li L, Wang HZ, Valiunas V, Richard G, Brink PR, White TW. The Cx26-G45E mutation displays increased hemichannel activity in a mouse model of the lethal form of keratitis-ichthyosis-deafness syndrome. Mol Biol Cell. 2011 Dec; 22(24):4776-86.
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Lazic T, Li Q, Frank M, Uitto J, Zhou LH. Extending the phenotypic spectrum of keratitis-ichthyosis-deafness syndrome: report of a patient with GJB2 (G12R) Connexin 26 mutation and unusual clinical findings. Pediatr Dermatol. 2012 May-Jun; 29(3):349-57.
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Ndumele CD, Ableman G, Russell BE, Gurrola E, Hicks LS. Publication of recruitment methods in focus group research of minority populations with chronic disease: a systematic review. J Health Care Poor Underserved. 2011 Feb; 22(1):5-23.