Zobrazeno 1 - 10
of 435
pro vyhledávání: '"Byung-Yoon Choi"'
Autor:
Bong Jik Kim, Yujin Kim, Ju Ang Kim, Jin Hee Han, Min Young Kim, Hee Kyung Yang, Chae-Seo Rhee, Young Cheol Kang, Chun-Hyung Kim, Byung Yoon Choi
Publikováno v:
Clinical and Experimental Otorhinolaryngology, Vol 17, Iss 3, Pp 206-216 (2024)
Objectives. FDXR encodes mitochondrial ferredoxin reductase, which is associated with auditory neuropathy spectrum disorder (ANSD) and optic atrophy. To date, only two studies have described FDXR-related hearing loss. The auditory rehabilitation outc
Externí odkaz:
https://doaj.org/article/d2768fa8e0724587aefeb51ed2cca886
Autor:
Seung Jae Lee, Heonjeong Oh, Kyu Ha Shin, Sung-Min Park, Yun Kyeong Kim, Do Hyun Jung, Jiyeon Yang, Yejun Chun, Min Young Kim, Jin Hee Han, Ju Ang Kim, Ngoc-Trinh Tran, Bong Jik Kim, Byung Yoon Choi
Publikováno v:
Clinical and Experimental Otorhinolaryngology, Vol 17, Iss 1, Pp 46-55 (2024)
Objectives. The recent expansion of eligibility for cochlear implantation (CI) by the U.S. Food and Drug Administration (FDA) to include infants as young as 9 months has reignited debates concerning the clinically appropriate cut-off age for pediatri
Externí odkaz:
https://doaj.org/article/93b8e84301e643a89a6a43961308cac1
Autor:
Dong Woo Nam, Yong Keun Song, Jeong Hun Kim, Eun Kyoung Lee, Kyu Hyung Park, JuHyuen Cha, Byung Yoon Choi, Jun Ho Lee, Seung Ha Oh, Dong Hyun Jo, Sang-Yeon Lee
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-14 (2023)
Abstract When medical genetic syndromes are influenced by allelic hierarchies, mutant alleles have distinct effects on clinical phenotypes. Genotype–phenotype correlations for Usher syndrome type 2 (USH2) suggest that the USH2A gene exhibits an all
Externí odkaz:
https://doaj.org/article/89e214d741cc4a1dbaf3418deb57ab8b
Autor:
Sang-Yeon Lee, Min Young Kim, Jin Hee Han, Sang Soo Park, Yejin Yun, Seung-Cheol Jee, Jae Joon Han, Jun Ho Lee, Heeyoung Seok, Byung Yoon Choi
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-14 (2023)
Abstract POU4F3, a member of the POU family of transcription factors, commonly causes autosomal dominant deafness. Exome sequencing was used to identify four novel variants in POU4F3 (NM_002700.2), including c.564dupA: p.Ala189SerfsTer26, c.743T > C:
Externí odkaz:
https://doaj.org/article/9c67b1fd58ab4b5b843076a19b199600
Autor:
Min-Ku Kim, So-Yeon Yun, Seonkyung Lee, Ja-Ok Lee, Soo-Yun Sung, Ju-Young Lee, Hyo-Jung Kim, Hye Youn Park, Jeong-Yoon Choi, Jae-Jin Song, Byung Yoon Choi, Ja-Won Koo, Ji-Soo Kim
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
Background and purposeCustomized vestibular rehabilitation improved dizziness and imbalance in several randomized controlled trials. In the present study, we determined the efficacy of customized vestibular rehabilitation using real-world observation
Externí odkaz:
https://doaj.org/article/3296ed83ce0c4f7d8091c670cbf65a5d
Autor:
Somin Lee, Yejin Yun, Ju Hyuen Cha, Jin Hee Han, Dae Hee Lee, Jae-Jin Song, Moo Kyun Park, Jun Ho Lee, Seung Ha Oh, Byung Yoon Choi, Sang-Yeon Lee
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-15 (2023)
Abstract Branchio-oto-renal (BOR)/branchio-otic (BO) syndrome is a rare disorder and exhibits clinically heterogenous phenotypes, marked by abnormalities in the ear, branchial arch, and renal system. Sporadic cases of atypical BOR/BO syndrome have be
Externí odkaz:
https://doaj.org/article/7877d998df4b40d28ae47aec50d32678
Autor:
Goun Choe, Jong Woo Lim, Hyun Jung Lee, Seung Hyun Kim, Marge Carandang, Bong Jik Kim, Byung Yoon Choi
Publikováno v:
PLoS ONE, Vol 19, Iss 2, p e0297640 (2024)
This study aimed to compare the development of pronunciation in South Korean preschoolers with unilateral cochlear nerve deficiency (CND) to that of age-matched preschoolers with normal hearing, a topic that has not been explored previously. In a ret
Externí odkaz:
https://doaj.org/article/43b7805698574f15b417623b54a8a9c9
Autor:
Yehree Kim, Byung Yoon Choi
Publikováno v:
Clinical and Experimental Otorhinolaryngology, Vol 15, Iss 4, Pp 299-309 (2022)
In the early days of cochlear implantation (CI) surgery, when the types of electrodes were limited and the etiology of sensorineural hearing loss (SNHL) was not well understood, the one-size-fits-all approach to CI held true, as in all other fields.
Externí odkaz:
https://doaj.org/article/402fe156ff9649b9a8ebbd81dac05648
Autor:
So Young Kim, Bong Jik Kim, Doo Yi Oh, Jin Hee Han, Nayoung Yi, Namju Justin Kim, Moo Kyun Park, Changwon Keum, Go Hun Seo, Byung Yoon Choi
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-9 (2022)
Abstract The 2018 Hearing Loss Expert Panel (HL-EP)-specific guidelines specified from the universal 2015 ACMG/AMP guidelines are proposed to be used in genetic HL, which prompted this study. A genetic HL cohort comprising 135 unrelated probands with
Externí odkaz:
https://doaj.org/article/b22ed8b2ba0840258707c314be04aa1d
Autor:
Young Seok Kim, Yoonjoong Kim, Hyoung Won Jeon, Nayoung Yi, Sang-Yeon Lee, Yehree Kim, Jin Hee Han, Min Young Kim, Bo Hye Kim, Hyeong Yun Choi, Marge Carandang, Ja-Won Koo, Bong Jik Kim, Yun Jung Bae, Byung Yoon Choi
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-9 (2022)
Abstract Determining the etiology of severe-to-profound sensorineural hearing loss (SP-SNHL) in pediatric subjects is particularly important in aiding the decision for auditory rehabilitation. We aimed to update the etiologic spectrum of pediatric SP
Externí odkaz:
https://doaj.org/article/6c2fd5f5a19449d793b6d50fdeaadf38