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Seung Ha Oh

Showing results (221-230 of 235) with videos related to

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Plos One|January 30, 2018
The diagnostic performance of a novel ELISA for human CTP (Cochlin-tomoprotein) to detect perilymph leakageTetsuo Ikezono, Tomohiro Matsumura, Han Matsuda, et al.
Plos One|February 11, 2015
Downsloping high-frequency hearing loss due to inner ear tricellular tight junction disruption by a novel ILDR1 mutation in the Ig-like domainNayoung K D Kim, Tomohito Higashi, Kyoung Yeul Lee, et al.
Rheumatology (Oxford, England)|October 6, 2020
Otological aspects of NLRP3-related autoinflammatory disorder focusing on the responsiveness to anakinraBong Jik Kim, Young Ho Kim, Seungmin Lee, et al.
Biomed Research International|September 20, 2018
Characterization of Detailed Audiological Features of Cytomegalovirus Infection: A Composite Cohort Study from Groups with Distinct DemographicsBong Jik Kim, Jae Joon Han, Seung Han Shin, et al.
Journal of Neuroscience Research|February 16, 2006
Immunohistochemical study of the distribution of sodium-dependent vitamin C transporters in adult rat brainGa Hee Mun, Myeung Ju Kim, Ju Hyun Lee, et al.
Plos One|October 30, 2016
Discovery of CDH23 as a Significant Contributor to Progressive Postlingual Sensorineural Hearing Loss in KoreansBong Jik Kim, Ah Reum Kim, Chung Lee, et al.
Scientific Reports|February 9, 2019
Elucidation of the unique mutation spectrum of severe hearing loss in a Vietnamese pediatric populationJae Joon Han, Pham Dinh Nguyen, Doo-Yi Oh, et al.
Genetic Testing and Molecular Biomarkers|August 4, 2009
Efficient molecular genetic diagnosis of enlarged vestibular aqueducts in East AsiansByung Yoon Choi, Andrew K Stewart, Katherine K Nishimura, et al.
Biomed Research International|September 20, 2022
Effects of CoQ10 Replacement Therapy on the Audiological Characteristics of Pediatric Patients with <i>COQ6</i> VariantsDong Woo Nam, Sang Soo Park, So Min Lee, et al.
Scientific Reports|November 30, 2017
ATP1A3 mutations can cause progressive auditory neuropathy: a new gene of auditory synaptopathyKyu-Hee Han, Doo-Yi Oh, Seungmin Lee, et al.
Pageof 24

Showing results (221-230 of 235) with videos related to

Sort By:
Pageof 24
Plos One|January 30, 2018
The diagnostic performance of a novel ELISA for human CTP (Cochlin-tomoprotein) to detect perilymph leakageTetsuo Ikezono, Tomohiro Matsumura, Han Matsuda, et al.
Plos One|February 11, 2015
Downsloping high-frequency hearing loss due to inner ear tricellular tight junction disruption by a novel ILDR1 mutation in the Ig-like domainNayoung K D Kim, Tomohito Higashi, Kyoung Yeul Lee, et al.
Rheumatology (Oxford, England)|October 6, 2020
Otological aspects of NLRP3-related autoinflammatory disorder focusing on the responsiveness to anakinraBong Jik Kim, Young Ho Kim, Seungmin Lee, et al.
Biomed Research International|September 20, 2018
Characterization of Detailed Audiological Features of Cytomegalovirus Infection: A Composite Cohort Study from Groups with Distinct DemographicsBong Jik Kim, Jae Joon Han, Seung Han Shin, et al.
Journal of Neuroscience Research|February 16, 2006
Immunohistochemical study of the distribution of sodium-dependent vitamin C transporters in adult rat brainGa Hee Mun, Myeung Ju Kim, Ju Hyun Lee, et al.
Plos One|October 30, 2016
Discovery of CDH23 as a Significant Contributor to Progressive Postlingual Sensorineural Hearing Loss in KoreansBong Jik Kim, Ah Reum Kim, Chung Lee, et al.
Scientific Reports|February 9, 2019
Elucidation of the unique mutation spectrum of severe hearing loss in a Vietnamese pediatric populationJae Joon Han, Pham Dinh Nguyen, Doo-Yi Oh, et al.
Genetic Testing and Molecular Biomarkers|August 4, 2009
Efficient molecular genetic diagnosis of enlarged vestibular aqueducts in East AsiansByung Yoon Choi, Andrew K Stewart, Katherine K Nishimura, et al.
Biomed Research International|September 20, 2022
Effects of CoQ10 Replacement Therapy on the Audiological Characteristics of Pediatric Patients with <i>COQ6</i> VariantsDong Woo Nam, Sang Soo Park, So Min Lee, et al.
Scientific Reports|November 30, 2017
ATP1A3 mutations can cause progressive auditory neuropathy: a new gene of auditory synaptopathyKyu-Hee Han, Doo-Yi Oh, Seungmin Lee, et al.
Pageof 24