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ArticlesPeer ReviewedFull Text
Inhaled amikacin for treatment of refractory pulmonary nontuberculous mycobacterial disease
Author / Creator:Olivier, Kenneth N ; Shaw, Pamela A ; Glaser, Tanya S ; Bhattacharyya, Darshana ; Fleshner, Michelle ; Brewer, Carmen C ; Zalewski, Christopher K ; Folio, Les R ; Siegelman, Jenifer R ; Shallom, Shamira ; Park, In Kwon ; Sampaio, Elizabeth P ; Zelazny, Adrian M ; Holland, Steven M ; Prevots, D Rebecca
Publisher:United States: American Thoracic Society
Journal title:Annals of the American Thoracic Society, 2014-01, Vol.11 (1), p.30-35
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Proposed therapy, developed in a Pcdh15 -deficient mouse, for progressive loss of vision in human Usher syndrome
Author / Creator:Sethna, Saumil ; Zein, Wadih M ; Riaz, Sehar ; Giese, Arnaud Pj ; Schultz, Julie M ; Duncan, Todd ; Hufnagel, Robert B ; Brewer, Carmen C ; Griffith, Andrew J ; Redmond, T Michael ; Riazuddin, Saima ; Friedman, Thomas B ; Ahmed, Zubair M
Publisher:England: eLife Sciences Publications Ltd
Journal title:eLife, 2021-11, Vol.10
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Characterization of hearing-impairment in Generalized Arterial Calcification of Infancy (GACI)
Author / Creator:Theng, Elizabeth H ; Brewer, Carmen C ; Oheim, Ralf ; Zalewski, Christopher K ; King, Kelly A ; Delsmann, Maximillian M ; Rolvien, Tim ; Gafni, Rachel I ; Braddock, Demetrios T ; Jeffrey Kim, H ; Ferreira, Carlos R
Publisher:England: BioMed Central Ltd
Journal title:Orphanet journal of rare diseases, 2022-07, Vol.17 (1), p.273-273, Article 273
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Mechanisms of hearing loss in neurofibromatosis type 2
Author / Creator:Asthagiri, Ashok R ; Vasquez, Raul A ; Butman, John A ; Wu, Tianxia ; Morgan, Keaton ; Brewer, Carmen C ; King, Kelly ; Zalewski, Chris ; Kim, H Jeffrey ; Lonser, Russell R
Publisher:United States: Public Library of Science
Journal title:PloS one, 2012-09, Vol.7 (9), p.e46132-e46132
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SLC26A4-linked CEVA haplotype correlates with phenotype in patients with enlargement of the vestibular aqueduct
Author / Creator:Chao, Janet R ; Chattaraj, Parna ; Munjal, Tina ; Honda, Keiji ; King, Kelly A ; Zalewski, Christopher K ; Chien, Wade W ; Brewer, Carmen C ; Griffith, Andrew J
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genetics, 2019-07, Vol.20 (1), p.118-118, Article 118
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Differences in peripheral neuropathy in xeroderma pigmentosum complementation groups A and D as evaluated by nerve conduction studies
Author / Creator:Lehky, Tanya J. ; Sackstein, Paul ; Tamura, Deborah ; Quezado, Martha ; Wu, Tianxia ; Khan, Sikandar G. ; Patronas, Nicholas J. ; Wiggs, Edythe ; Brewer, Carmen C. ; DiGiovanna, John J. ; Kraemer, Kenneth H.
Publisher:London: BioMed Central Ltd
Journal title:BMC neurology, 2021-10, Vol.21 (1), p.1-393, Article 393
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Carmen C. Brewer, Christopher Zalewski, and Kelly King, audiologists and members of the National Institute on Deafness and Other Communication Disorders Audiology Unit, received the National Institute...
Publisher:American Speech-Language-Hearing Association
Journal title:ASHA leader, 2012-09, Vol.17 (11), p.34
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Intrathecal 2-hydroxypropyl-β-cyclodextrin decreases neurological disease progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1–2 trial
Author / Creator:Ory, Daniel S ; Ottinger, Elizabeth A ; Farhat, Nicole Yanjanin ; King, Kelly A ; Jiang, Xuntian ; Weissfeld, Lisa ; Berry-Kravis, Elizabeth ; Davidson, Cristin D ; Bianconi, Simona ; Keener, Lee Ann ; Rao, Ravichandran ; Soldatos, Ariane ; Sidhu, Rohini ; Walters, Kimberly A ; Xu, Xin ; Thurm, Audrey ; Solomon, Beth ; Pavan, William J ; Machielse, Bernardus N ; Kao, Mark ; Silber, Steven A ; McKew, John C ; Brewer, Carmen C ; Vite, Charles H ; Walkley, Steven U ; Austin, Christopher P ; Porter, Forbes D
Publisher:England: Elsevier Ltd
Journal title:The Lancet (British edition), 2017-10, Vol.390 (10104), p.1758-1768
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Genetic hearing loss: the audiologist’s perspective
Author / Creator:Brewer, Carmen C. ; King, Kelly A.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Human genetics, 2022-04, Vol.141 (3-4), p.311-314
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ArticlesPeer ReviewedFull Text
NLRP3 mutation and cochlear autoinflammation cause syndromic and nonsyndromic hearing loss DFNA34 responsive to anakinra therapy
Author / Creator:Nakanishi, Hiroshi ; Kawashima, Yoshiyuki ; Kurima, Kiyoto ; Chae, Jae Jin ; Ross, Astin M. ; Pinto-Patarroyo, Gineth ; Patel, Seema K. ; Muskett, Julie A. ; Ratay, Jessica S. ; Chattaraj, Parna ; Park, Yong Hwan ; Grevich, Sriharsha ; Brewer, Carmen C. ; Hoa, Michael ; Kim, H. Jeffrey ; Butman, John A. ; Broderick, Lori ; Hoffman, Hal M. ; Aksentijevich, Ivona ; Kastner, Daniel L. ; Goldbach-Mansky, Raphaela ; Griffith, Andrew J.
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2017-09, Vol.114 (37), p.E7766-E7775
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Report of a SPEAC webinar 22 september 2023: Sensorineural hearing loss, lassa virus disease and vaccines
Author / Creator:Reed, Nicholas S ; Brewer, Carmen C ; Akintunde, Gideon ; Blackie, Faustina F ; Charles, Lovelyn ; Fast, Patricia ; Lambert, Paul-Henri ; Okogbenin, Sylvanus ; Paessler, Slobodan ; Pinschewer, Daniel D ; Top, Karina A ; Black, Steven B ; Dekker, Cornelia L
Publisher:Netherlands: Elsevier Ltd
Journal title:Vaccine, 2025-01, Vol.43 (Pt 1), p.126525-126525, Article 126525
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ArticlesPeer ReviewedFull Text
CHD7 variants associated with hearing loss and enlargement of the vestibular aqueduct
Author / Creator:Roux, Isabelle ; Fenollar-Ferrer, Cristina ; Lee, Hyun Jae ; Chattaraj, Parna ; Lopez, Ivan A. ; Han, Kyungreem ; Honda, Keiji ; Brewer, Carmen C. ; Butman, John A. ; Morell, Robert J. ; Martin, Donna M. ; Griffith, Andrew J.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Human genetics, 2023-10, Vol.142 (10), p.1499-1517
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ArticlesPeer ReviewedFull Text
Heritability of non-speech auditory processing skills
Author / Creator:Brewer, Carmen C ; Zalewski, Christopher K ; King, Kelly A ; Zobay, Oliver ; Riley, Alison ; Ferguson, Melanie A ; Bird, Jonathan E ; McCabe, Margaret M ; Hood, Linda J ; Drayna, Dennis ; Griffith, Andrew J ; Morell, Robert J ; Friedman, Thomas B ; Moore, David R
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2016-08, Vol.24 (8), p.1137-1144
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Audiovestibular Findings in a Cohort of Patients with Chiari Malformation Type I and Dizziness
Author / Creator:Famili, Hannah P ; Zalewski, Christopher K ; Ibrahimy, Alaaddin ; Mack, Jessica ; Cantor, Fredric ; Heiss, John D ; Brewer, Carmen C
Publisher:Switzerland: MDPI AG
Journal title:Journal of clinical medicine, 2023-04, Vol.12 (8), p.2767
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Clinical Considerations for Routine Auditory and Vestibular Monitoring in Patients With Cystic Fibrosis
Author / Creator:Garinis, Angela C ; Poling, Gayla L ; Rubenstein, Ronald C ; Konrad-Martin, Dawn ; Hullar, Timothy E ; Baguley, David M ; Burrows, Holly L ; Chisholm, Jennifer A ; Custer, Amy ; Hawe, Laura Dreisbach ; Hunter, Lisa L ; Marras, Theodore K ; Ortiz, Candice E ; Petersen, Lucretia ; Steyger, Peter S ; Winthrop, Kevin ; Zettner, Erika M ; Clark, Khaya ; Hungerford, Michelle ; Vachhani, Jay J ; Brewer, Carmen C
Publisher:United States: American Speech-Language-Hearing Association
Journal title:American journal of audiology, 2021-10, Vol.30 (3S), p.800-809
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Auditory Phenotype of Smith-Magenis Syndrome
Author / Creator:Brendal, Megan A ; King, Kelly A ; Zalewski, Christopher K ; Finucane, Brenda M ; Introne, Wendy ; Brewer, Carmen C ; Smith, Ann C. M
Publisher:United States: American Speech-Language-Hearing Association
Journal title:Journal of speech, language, and hearing research, 2017-04, Vol.60 (4), p.1076-1087
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Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p
Author / Creator:Rehman, Atteeq U. ; Gul, Khitab ; Morell, Robert J. ; Lee, Kwanghyuk ; Ahmed, Zubair M. ; Riazuddin, Saima ; Ali, Rana A. ; Shahzad, Mohsin ; Jaleel, Ateeq-ul ; Andrade, Paula B. ; Khan, Shaheen N. ; Khan, Saadullah ; Brewer, Carmen C. ; Ahmad, Wasim ; Leal, Suzanne M. ; Riazuddin, Sheikh ; Friedman, Thomas B.
Publisher:Berlin/Heidelberg: Springer-Verlag
Journal title:Human genetics, 2011-12, Vol.130 (6), p.759-765
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Hearing Loss is an Early Consequence of Npc1 Gene Deletion in the Mouse Model of Niemann–Pick Disease, Type C
Author / Creator:King, Kelly A. ; Gordon-Salant, Sandra ; Pawlowski, Karen S. ; Taylor, Anna M. ; Griffith, Andrew J. ; Houser, Ari ; Kurima, Kiyoto ; Wassif, Christopher A. ; Wright, Charles G. ; Porter, Forbes D. ; Repa, Joyce J. ; Brewer, Carmen C.
Publisher:Boston: Springer US
Journal title:Journal of the Association for Research in Otolaryngology, 2014-08, Vol.15 (4), p.529-541
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A twin study of auditory processing indicates that dichotic listening ability is a strongly heritable trait
Author / Creator:MORELL, Robert J ; BREWER, Carmen C ; DONGLIANG GE ; SNIEDER, Harold ; ZALEWSKI, Christopher K ; KING, Kelly A ; DRAYNA, Dennis ; FRIEDMAN, Thomas B
Publisher:Heidelberg: Springer
Journal title:Human genetics, 2007-08, Vol.122 (1), p.103-111
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A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome
Author / Creator:Di Gioia, Silvio Alessandro ; Connors, Samantha ; Matsunami, Norisada ; Cannavino, Jessica ; Rose, Matthew F. ; Gilette, Nicole M. ; Artoni, Pietro ; de Macena Sobreira, Nara Lygia ; Chan, Wai-Man ; Webb, Bryn D. ; Robson, Caroline D. ; Cheng, Long ; Van Ryzin, Carol ; Ramirez-Martinez, Andres ; Mohassel, Payam ; Leppert, Mark ; Scholand, Mary Beth ; Grunseich, Christopher ; Ferreira, Carlos R. ; Hartman, Tyler ; Hayes, Ian M. ; Morgan, Tim ; Markie, David M. ; Fagiolini, Michela ; Swift, Amy ; Chines, Peter S. ; Speck-Martins, Carlos E. ; Collins, Francis S. ; Jabs, Ethylin Wang ; Bönnemann, Carsten G. ; Olson, Eric N. ; Carey, John C. ; Robertson, Stephen P. ; Manoli, Irini ; Engle, Elizabeth C.
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2017-07, Vol.8 (1), p.16077-16, Article 16077
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Showing 1 to 20 of 31 results

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Inhaled amikacin for treatment of refractory pulmonary nontuberculous mycobacterial disease

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Proposed therapy, developed in a Pcdh15 -deficient mouse, for progressive loss of vision in human Usher syndrome

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Characterization of hearing-impairment in Generalized Arterial Calcification of Infancy (GACI)

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Mechanisms of hearing loss in neurofibromatosis type 2

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SLC26A4-linked CEVA haplotype correlates with phenotype in patients with enlargement of the vestibular aqueduct

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Differences in peripheral neuropathy in xeroderma pigmentosum complementation groups A and D as evaluated by nerve conduction studies

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Carmen C. Brewer, Christopher Zalewski, and Kelly King, audiologists and members of the National Institute on Deafness and Other Communication Disorders Audiology Unit, received the National Institute...

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Intrathecal 2-hydroxypropyl-β-cyclodextrin decreases neurological disease progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1–2 trial

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Genetic hearing loss: the audiologist’s perspective

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NLRP3 mutation and cochlear autoinflammation cause syndromic and nonsyndromic hearing loss DFNA34 responsive to anakinra therapy

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Report of a SPEAC webinar 22 september 2023: Sensorineural hearing loss, lassa virus disease and vaccines

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CHD7 variants associated with hearing loss and enlargement of the vestibular aqueduct

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Heritability of non-speech auditory processing skills

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Audiovestibular Findings in a Cohort of Patients with Chiari Malformation Type I and Dizziness

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Clinical Considerations for Routine Auditory and Vestibular Monitoring in Patients With Cystic Fibrosis

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Auditory Phenotype of Smith-Magenis Syndrome

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Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p

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Hearing Loss is an Early Consequence of Npc1 Gene Deletion in the Mouse Model of Niemann–Pick Disease, Type C

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A twin study of auditory processing indicates that dichotic listening ability is a strongly heritable trait

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A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome

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