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Kelly A King

Showing results (21-30 of 45) with videos related to

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Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|June 4, 2019
Audiologic and Otologic Complications of Cryptococcal Meningoencephalitis in Non-HIV Previously Healthy PatientsKelly A King, Ghedak Ansari, Anil A Panackal, et al.
Advances in Oto-Rhino-Laryngology|March 2, 2011
Hereditary hearing loss with thyroid abnormalitiesByung Yoon Choi, Julie Muskett, Kelly A King, et al.
Orphanet Journal of Rare Diseases|July 19, 2022
Characterization of hearing-impairment in Generalized Arterial Calcification of Infancy (GACI)Elizabeth H Theng, Carmen C Brewer, Ralf Oheim, et al.
Ophthalmic Genetics|May 7, 2020
Atypical and ultra-rare Usher syndrome: a reviewRosalie M Nolen, Robert B Hufnagel, Thomas B Friedman, et al.
World Journal of Otorhinolaryngology|May 12, 2015
<i>SLC26A4</i> mutation testing for hearing loss associated with enlargement of the vestibular aqueductTaku Ito, Julie Muskett, Parna Chattaraj, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|November 26, 2011
SLC26A4 genotypes and phenotypes associated with enlargement of the vestibular aqueductTaku Ito, Byung Yoon Choi, Kelly A King, et al.
Journal of the Association for Research in Otolaryngology : JARO|May 20, 2014
Hearing loss is an early consequence of Npc1 gene deletion in the mouse model of Niemann-Pick disease, type CKelly A King, Sandra Gordon-Salant, Karen S Pawlowski, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|May 19, 2012
Audiovestibular dysfunction associated with adoptive cell immunotherapy for melanomaBradley J Seaman, Elizabeth A Guardiani, Carmen C Brewer, et al.
Clinical Genetics|October 22, 2020
Vestibular phenotype-genotype correlation in a cohort of 90 patients with Usher syndromeTalah T Wafa, Rabia Faridi, Kelly A King, et al.
The Laryngoscope|December 10, 2009
SLC26A4 genotype, but not cochlear radiologic structure, is correlated with hearing loss in ears with an enlarged vestibular aqueductKelly A King, Byung Yoon Choi, Christopher Zalewski, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|June 4, 2019
Audiologic and Otologic Complications of Cryptococcal Meningoencephalitis in Non-HIV Previously Healthy PatientsKelly A King, Ghedak Ansari, Anil A Panackal, et al.
Advances in Oto-Rhino-Laryngology|March 2, 2011
Hereditary hearing loss with thyroid abnormalitiesByung Yoon Choi, Julie Muskett, Kelly A King, et al.
Orphanet Journal of Rare Diseases|July 19, 2022
Characterization of hearing-impairment in Generalized Arterial Calcification of Infancy (GACI)Elizabeth H Theng, Carmen C Brewer, Ralf Oheim, et al.
Ophthalmic Genetics|May 7, 2020
Atypical and ultra-rare Usher syndrome: a reviewRosalie M Nolen, Robert B Hufnagel, Thomas B Friedman, et al.
World Journal of Otorhinolaryngology|May 12, 2015
<i>SLC26A4</i> mutation testing for hearing loss associated with enlargement of the vestibular aqueductTaku Ito, Julie Muskett, Parna Chattaraj, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|November 26, 2011
SLC26A4 genotypes and phenotypes associated with enlargement of the vestibular aqueductTaku Ito, Byung Yoon Choi, Kelly A King, et al.
Journal of the Association for Research in Otolaryngology : JARO|May 20, 2014
Hearing loss is an early consequence of Npc1 gene deletion in the mouse model of Niemann-Pick disease, type CKelly A King, Sandra Gordon-Salant, Karen S Pawlowski, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|May 19, 2012
Audiovestibular dysfunction associated with adoptive cell immunotherapy for melanomaBradley J Seaman, Elizabeth A Guardiani, Carmen C Brewer, et al.
Clinical Genetics|October 22, 2020
Vestibular phenotype-genotype correlation in a cohort of 90 patients with Usher syndromeTalah T Wafa, Rabia Faridi, Kelly A King, et al.
The Laryngoscope|December 10, 2009
SLC26A4 genotype, but not cochlear radiologic structure, is correlated with hearing loss in ears with an enlarged vestibular aqueductKelly A King, Byung Yoon Choi, Christopher Zalewski, et al.
Pageof 5