Zoekresultaten - King, Kelly A.
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Genetic hearing loss: the audiologist’s perspective door Brewer, Carmen C., King, Kelly A.
Gepubliceerd in 2022Text -
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Hearing safety from single- and double-pulse transcranial magnetic stimulation in children and young adults door Kukke, Sahana N., Brewer, Carmen C., Zalewski, Christopher, King, Kelly A., Damiano, Diane, Alter, Katharine E., Hallett, Mark
Gepubliceerd in 2017Text -
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Cryopyrin-Associated Periodic Syndromes: Otolaryngologic and Audiologic Manifestations door Ahmadi, Neda, Brewer, Carmen C., Zalewski, Christopher, King, Kelly A., Butman, John A., Plass, Nicole, Henderson, Cailin, Goldbach-Mansky, Raphaela, Kim, H. Jeffrey
Gepubliceerd in 2011Text -
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SLC26A4-linked CEVA haplotype correlates with phenotype in patients with enlargement of the vestibular aqueduct door Chao, Janet R., Chattaraj, Parna, Munjal, Tina, Honda, Keiji, King, Kelly A., Zalewski, Christopher K., Chien, Wade W., Brewer, Carmen C., Griffith, Andrew J.
Gepubliceerd in 2019Text -
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Audiologic Natural History of Small Volume Cochleovestibular Schwannomas in Neurofibromatosis Type 2 door deTorres, Alvin T., Brewer, Carmen C., Zalewski, Chris K., King, Kelly A., Walker, Robert, Scott, Gretchen C., Asthagiri, Ashok R., Chittiboina, Prashant, Kim, H. Jeffrey
Gepubliceerd in 2018Text -
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Auditory and Otologic Profile of Alström Syndrome: Comprehensive Single Center Data on 38 Patients door Lindsey, Spencer, Brewer, Carmen, Stakhovskaya, Olga, Kim, H Jeffrey, Zalewski, Chris, Bryant, Joy, King, Kelly A., Naggert, Jürgen K., Gahl, William A, Marshall, Jan D., Gunay-Aygun, Meral
Gepubliceerd in 2017Text -
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Hearing Loss Associated with Enlarged Vestibular Aqueduct and Zero or One Mutant Allele of SLC26A4 door Rose, Jane, Muskett, Julie A., King, Kelly A., Zalewski, Christopher K., Chattaraj, Parna, Butman, John A., Kenna, Margaret A., Chien, Wade W., Brewer, Carmen C., Griffith, Andrew J.
Gepubliceerd in 2016Text -
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Audiologic and Otologic Complications of Cryptococcal Meningoencephalitis in Non-HIV Previously Healthy Patients door King, Kelly A., Ansari, Ghedak, Panackal, Anil A., Zalewski, Chris, Anjum, Seher, Bennett, John E., Beri, Andrea, Kim, H. Jeff, Hammoud, Dima, Brewer, Carmen C., Williamson, Peter R.
Gepubliceerd in 2019Text -
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Characterization of hearing-impairment in Generalized Arterial Calcification of Infancy (GACI) door 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.
Gepubliceerd in 2022Text -
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Atypical and Ultra-rare Usher Syndrome: A Review door Nolen, Rosalie M., Hufnagel, Robert B., Friedman, Thomas B., Turriff, Amy E., Brewer, Carmen C., Zalewski, Christopher K., King, Kelly A., Wafa, Talah, Griffith, Andrew J., Brooks, Brian, Zein, Wadih M.
Gepubliceerd in 2020Text -
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Hearing Loss is an Early Consequence of Npc1 Gene Deletion in the Mouse Model of Niemann–Pick Disease, Type C door 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.
Gepubliceerd in 2014Text -
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SLC26A4 mutation testing for hearing loss associated with enlargement of the vestibular aqueduct door Ito, Taku, Muskett, Julie, Chattaraj, Parna, Choi, Byung Yoon, Lee, Kyu Yup, Zalewski, Christopher K, King, Kelly A, Li, Xiangming, Wangemann, Philine, Shawker, Thomas, Brewer, Carmen C, Alper, Seth L, Griffith, Andrew J
Gepubliceerd in 2013Text -
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SLC26A4 Genotypes and Phenotypes Associated with Enlargement of the Vestibular Aqueduct door Ito, Taku, Choi, Byung Yoon, King, Kelly A., Zalewski, Christopher K., Muskett, Julie, Chattaraj, Parna, Shawker, Thomas, Reynolds, James C., Butman, John A., Brewer, Carmen C., Wangemann, Philine, Alper, Seth L., Griffith, Andrew J.
Gepubliceerd in 2011Text