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Hyaluronan Synthase 1: A Novel Candidate Gene Associated With Late-Onset Non-syndromic Hereditary Hearing Loss
Alphonse Umugire, Sungsu Lee, Chang-Joon Lee, Youngmi Choi, Taekyoung Kim, Hyong-Ho Cho
Clin Exp Otorhinolaryngol. 2022;15(3):220-229.   Published online April 8, 2022
DOI: https://doi.org/10.21053/ceo.2022.00038
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Severe or Profound Sensorineural Hearing Loss Caused by Novel USH2A Variants in Korea: Potential Genotype-Phenotype Correlation
Sang-Yeon Lee, Kwangsic Joo, Jayoung Oh, Jin Hee Han, Hye-Rim Park, Seungmin Lee, Doo-Yi Oh, Se Joon Woo, Byung Yoon Choi
Clin Exp Otorhinolaryngol. 2020;13(2):113-122.   Published online November 2, 2019
DOI: https://doi.org/10.21053/ceo.2019.00990
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Two Compound Heterozygous Were Identified in SLC26A4 Gene in Two Chinese Families With Enlarged Vestibular Aqueduct
Yongbo Yu, Yang Yang, Jie Lu, Yaqiong Jin, Yeran Yang, Enyu Hong, Jin Shi, Feng Chen, Shujing Han, Ping Chu, Yongli Guo, Xin Ni
Clin Exp Otorhinolaryngol. 2019;12(1):50-57.   Published online August 9, 2018
DOI: https://doi.org/10.21053/ceo.2018.00213
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Predicting Extrathyroidal Extension in Patients With Papillary Thyroid Microcarcinoma According to a BRAF Mutation
Doh Young Lee, Soo Min Hwang, Jee Hyun An, Kyu Ri Son, Seung-Kuk Baek, Sin Gon Kim, Yang Seok Chae, Kwang-Yoon Jung
Clin Exp Otorhinolaryngol. 2017;10(2):174-180.   Published online July 2, 2016
DOI: https://doi.org/10.21053/ceo.2015.01655
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A Novel Frameshift Mutation of SLC26A4 in a Korean Family With Nonsyndromic Hearing Loss and Enlarged Vestibular Aqueduct
Borum Sagong, Jeong-In Baek, Kyu-Yup Lee, Un-Kyung Kim
Clin Exp Otorhinolaryngol. 2017;10(1):50-55.   Published online July 7, 2016
DOI: https://doi.org/10.21053/ceo.2016.00430
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Compound Heterozygosity for Two Novel SLC26A4 Mutations in a Large Iranian Pedigree with Pendred Syndrome
Nasrin Yazdanpanahi, Mohammad Amin Tabatabaiefar, Effat Farrokhi, Narges Abdian, Nader Bagheri, Shirin Shahbazi, Zahra Noormohammadi, Morteza Hashemzadeh Chaleshtori
Clin Exp Otorhinolaryngol. 2013;6(4):201-208.   Published online November 29, 2013
DOI: https://doi.org/10.3342/ceo.2013.6.4.201
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Syndromic Hearing Loss in Association with PTPN11-Related Disorder: The Experience of Cochlear Implantation in a Child with LEOPARD Syndrome
Ho-Suk Chu, Hae-Sun Chung, Moon-Hee Ko, Hee-Jin Kim, Chang-Seok Ki, Won-Ho Chung, Yang-Sun Cho, Sung Hwa Hong
Clin Exp Otorhinolaryngol. 2013;6(2):99-102.   Published online February 7, 2011
DOI: https://doi.org/10.3342/ceo.2013.6.2.99
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A Novel Frameshift Mutation of the USH2A Gene in a Korean Patient with Usher Syndrome Type II
Sung Hyun Boo, Min-Jung Song, Hee-Jin Kim, Yang-Sun Cho, Hosuk Chu, Moon-Hee Ko, Won-Ho Chung, Jong-Won Kim, Sung Hwa Hong
Clin Exp Otorhinolaryngol. 2013;6(1):41-44.   Published online October 1, 2011
DOI: https://doi.org/10.3342/ceo.2013.6.1.41
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Toll-like Receptors 2 and 4 and Their Mutations in Patients with Otitis Media and Middle Ear Effusion
Young Chan Lee, Chul Kim, Ju Sup Shim, Jae Yong Byun, Mun Suh Park, Chang Il Cha, Young Il Kim, Jin Woo Lee, Seung Geun Yeo
Clin Exp Otorhinolaryngol. 2008;1(4):189-195.   Published online December 26, 2008
DOI: https://doi.org/10.3342/ceo.2008.1.4.189
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  • Early Postoperative Benefits in Receptive and Expressive Language Development After Cochlear Implantation Under 9 Months of Age in Comparison to Implantation at Later Ages Clin Exp Otorhinolaryngol. 2024;17(1):46-55.
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