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Christopher K Zalewski

Showing results (11-20 of 33) with videos related to

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BMC Medical Genetics|July 4, 2019
SLC26A4-linked CEVA haplotype correlates with phenotype in patients with enlargement of the vestibular aqueductJanet R Chao, Parna Chattaraj, Tina Munjal, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 1, 2007
Cochlear implantation for hearing loss associated with bilateral endolymphatic sac tumors in von Hippel-Lindau diseaseJay Jagannathan, Russell R Lonser, Richard A Stanger, et al.
Pediatric Blood & Cancer|July 19, 2016
Otologic manifestations of Fanconi anemia and other inherited bone marrow failure syndromesAdedoyin Kalejaiye, Neelam Giri, Carmen C Brewer, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|April 11, 2014
Audiovestibular Characteristics of Small Cochleovestibular Schwannomas in Neurofibromatosis Type 2Michael A Holliday, Hung Jeffrey Kim, Christopher K Zalewski, et al.
The Laryngoscope|November 19, 2016
Hearing loss associated with enlarged vestibular aqueduct and zero or one mutant allele of SLC26A4Jane Rose, Julie A Muskett, Kelly A King, et al.
American Journal of Medical Genetics. Part A|June 15, 2007
Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domainTomoko Makishima, Anne C Madeo, Carmen C Brewer, 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.
The Journal of Clinical Endocrinology and Metabolism|October 25, 2012
Optic neuropathy in McCune-Albright syndrome: effects of early diagnosis and treatment of growth hormone excessAlison M Boyce, McKinley Glover, Marilyn H Kelly, 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.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
BMC Medical Genetics|July 4, 2019
SLC26A4-linked CEVA haplotype correlates with phenotype in patients with enlargement of the vestibular aqueductJanet R Chao, Parna Chattaraj, Tina Munjal, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 1, 2007
Cochlear implantation for hearing loss associated with bilateral endolymphatic sac tumors in von Hippel-Lindau diseaseJay Jagannathan, Russell R Lonser, Richard A Stanger, et al.
Pediatric Blood & Cancer|July 19, 2016
Otologic manifestations of Fanconi anemia and other inherited bone marrow failure syndromesAdedoyin Kalejaiye, Neelam Giri, Carmen C Brewer, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|April 11, 2014
Audiovestibular Characteristics of Small Cochleovestibular Schwannomas in Neurofibromatosis Type 2Michael A Holliday, Hung Jeffrey Kim, Christopher K Zalewski, et al.
The Laryngoscope|November 19, 2016
Hearing loss associated with enlarged vestibular aqueduct and zero or one mutant allele of SLC26A4Jane Rose, Julie A Muskett, Kelly A King, et al.
American Journal of Medical Genetics. Part A|June 15, 2007
Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domainTomoko Makishima, Anne C Madeo, Carmen C Brewer, 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.
The Journal of Clinical Endocrinology and Metabolism|October 25, 2012
Optic neuropathy in McCune-Albright syndrome: effects of early diagnosis and treatment of growth hormone excessAlison M Boyce, McKinley Glover, Marilyn H Kelly, 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.
Pageof 4