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Scientific Reports
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June 20, 2020
An integrative approach for pediatric auditory neuropathy spectrum disorders: revisiting etiologies and exploring the prognostic utility of auditory steady-state response
Pei-Hsuan Lin, Chuan-Jen Hsu, Yin-Hung Lin, et al.
Gene Therapy
|
September 4, 2024
CRISPR/Cas9-mediated exon skipping to restore premature translation termination in a DFNB4 mouse model
Chun-Ying Huang, Yi-Hsiu Tsai, Yi-Fen Cheng, et al.
Journal of Functional Biomaterials
|
January 27, 2026
Development and In Vivo Evaluation of a Novel Bioabsorbable Polylactic Acid Middle Ear Ventilation Tube
Ying-Chang Lu, Chi-Chieh Chang, Ping-Tun Teng, et al.
Ear and Hearing
|
June 28, 2019
Prediction Model for Audiological Outcomes in Patients With GJB2 Mutations
Pey-Yu Chen, Yin-Hung Lin, Tien-Chen Liu, et al.
Advanced Healthcare Materials
|
November 3, 2025
Porous Coatings by Vapor Sublimation and Deposition for Molecular Channeling and Filtration in an Interstitial Fluid Microfiltration Device
Yu-Ming Chang, Chi-Yu Huang, Yi-Jia Ke, et al.
Plos One
|
June 12, 2013
Differences in the pathogenicity of the p.H723R mutation of the common deafness-associated SLC26A4 gene in humans and mice
Ying-Chang Lu, Chen-Chi Wu, Ting-Hua Yang, et al.
JCI Insight
|
October 24, 2022
Gene therapy with a synthetic adeno-associated viral vector improves audiovestibular phenotypes in Pjvk-mutant mice
Ying-Chang Lu, Yi-Hsiu Tsai, Yen-Huei Chan, et al.
Scientific Reports
|
March 26, 2022
Prognostic determinants of hearing outcomes in children with congenital cytomegalovirus infection
Ta-Hsuan Lo, Pei-Hsuan Lin, Wei-Chung Hsu, et al.
Oral Oncology
|
September 28, 2011
Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas
Cheng-Ping Wang, Tseng-Cheng Chen, Yih-Leong Chang, et al.
International Journal of Molecular Sciences
|
July 12, 2025
Waardenburg Syndrome Type 4 in Mongolian Children: Genetic and Clinical Characterization
Bayasgalan Gombojav, Jargalkhuu Erdenechuluun, Tserendulam Batsaikhan, et al.
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Search research articles
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Showing results (61-70 of 112) with videos related to
Sort By:
Page
of 12
Scientific Reports
|
June 20, 2020
An integrative approach for pediatric auditory neuropathy spectrum disorders: revisiting etiologies and exploring the prognostic utility of auditory steady-state response
Pei-Hsuan Lin, Chuan-Jen Hsu, Yin-Hung Lin, et al.
Gene Therapy
|
September 4, 2024
CRISPR/Cas9-mediated exon skipping to restore premature translation termination in a DFNB4 mouse model
Chun-Ying Huang, Yi-Hsiu Tsai, Yi-Fen Cheng, et al.
Journal of Functional Biomaterials
|
January 27, 2026
Development and In Vivo Evaluation of a Novel Bioabsorbable Polylactic Acid Middle Ear Ventilation Tube
Ying-Chang Lu, Chi-Chieh Chang, Ping-Tun Teng, et al.
Ear and Hearing
|
June 28, 2019
Prediction Model for Audiological Outcomes in Patients With GJB2 Mutations
Pey-Yu Chen, Yin-Hung Lin, Tien-Chen Liu, et al.
Advanced Healthcare Materials
|
November 3, 2025
Porous Coatings by Vapor Sublimation and Deposition for Molecular Channeling and Filtration in an Interstitial Fluid Microfiltration Device
Yu-Ming Chang, Chi-Yu Huang, Yi-Jia Ke, et al.
Plos One
|
June 12, 2013
Differences in the pathogenicity of the p.H723R mutation of the common deafness-associated SLC26A4 gene in humans and mice
Ying-Chang Lu, Chen-Chi Wu, Ting-Hua Yang, et al.
JCI Insight
|
October 24, 2022
Gene therapy with a synthetic adeno-associated viral vector improves audiovestibular phenotypes in Pjvk-mutant mice
Ying-Chang Lu, Yi-Hsiu Tsai, Yen-Huei Chan, et al.
Scientific Reports
|
March 26, 2022
Prognostic determinants of hearing outcomes in children with congenital cytomegalovirus infection
Ta-Hsuan Lo, Pei-Hsuan Lin, Wei-Chung Hsu, et al.
Oral Oncology
|
September 28, 2011
Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas
Cheng-Ping Wang, Tseng-Cheng Chen, Yih-Leong Chang, et al.
International Journal of Molecular Sciences
|
July 12, 2025
Waardenburg Syndrome Type 4 in Mongolian Children: Genetic and Clinical Characterization
Bayasgalan Gombojav, Jargalkhuu Erdenechuluun, Tserendulam Batsaikhan, et al.
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of 12