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Dongyi Han

Showing results (111-120 of 141) with videos related to

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Nucleic Acids Research|February 22, 2005
Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing lossHui Zhao, Wie-Yen Young, Qingfeng Yan, et al.
Biochemical and Biophysical Research Communications|September 20, 2005
Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing lossLidong Zhao, Qiuju Wang, Yaping Qian, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|April 2, 2016
[A novel technique for simultaneous multi-gene mutation screening in 225 patients with nonsyndromic hearing loss]Di Zhang, Hong Duan, Peng Lin, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|July 13, 2021
Petrous bone cholesteatoma: our experience of 20 years and management of two giant cases affecting rhinopharynxYa Liu, Fangyuan Wang, Weidong Shen, et al.
American Journal of Medical Genetics. Part A|January 8, 2005
Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutationQiuju Wang, Roughua Li, Hui Zhao, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 14, 2018
Mutation spectra and founder effect of TMC1 in patients with non-syndromic deafness in Xiamen area, ChinaYi Jiang, Song Gao, Lihua Wu, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 14, 2017
Analysis and Management of Complications in a Cohort of 1,065 Minimally Invasive Cochlear ImplantationsYi Jiang, Ping Gu, Beicheng Li, et al.
Biochemical and Biophysical Research Communications|April 17, 2007
The mitochondrial tRNA(Ala) T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing lossDongyi Han, Pu Dai, Qingwen Zhu, et al.
Acta Oto-Laryngologica|July 25, 2022
Imaging features, staging system, and surgical management of giant cell lesions of the temporal boneXiaohong Li, Yi Wen, Jie Zhang, et al.
World Neurosurgery|June 23, 2026
Audiological characteristics and postoperative hearing preservation of vestibular schwannoma presenting with sudden hearing lossTianxing Zhang, Qiujing Zhang, Guojian Wang, et al.
Pageof 15

Showing results (111-120 of 141) with videos related to

Sort By:
Pageof 15
Nucleic Acids Research|February 22, 2005
Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing lossHui Zhao, Wie-Yen Young, Qingfeng Yan, et al.
Biochemical and Biophysical Research Communications|September 20, 2005
Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing lossLidong Zhao, Qiuju Wang, Yaping Qian, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|April 2, 2016
[A novel technique for simultaneous multi-gene mutation screening in 225 patients with nonsyndromic hearing loss]Di Zhang, Hong Duan, Peng Lin, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|July 13, 2021
Petrous bone cholesteatoma: our experience of 20 years and management of two giant cases affecting rhinopharynxYa Liu, Fangyuan Wang, Weidong Shen, et al.
American Journal of Medical Genetics. Part A|January 8, 2005
Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutationQiuju Wang, Roughua Li, Hui Zhao, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 14, 2018
Mutation spectra and founder effect of TMC1 in patients with non-syndromic deafness in Xiamen area, ChinaYi Jiang, Song Gao, Lihua Wu, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 14, 2017
Analysis and Management of Complications in a Cohort of 1,065 Minimally Invasive Cochlear ImplantationsYi Jiang, Ping Gu, Beicheng Li, et al.
Biochemical and Biophysical Research Communications|April 17, 2007
The mitochondrial tRNA(Ala) T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing lossDongyi Han, Pu Dai, Qingwen Zhu, et al.
Acta Oto-Laryngologica|July 25, 2022
Imaging features, staging system, and surgical management of giant cell lesions of the temporal boneXiaohong Li, Yi Wen, Jie Zhang, et al.
World Neurosurgery|June 23, 2026
Audiological characteristics and postoperative hearing preservation of vestibular schwannoma presenting with sudden hearing lossTianxing Zhang, Qiujing Zhang, Guojian Wang, et al.
Pageof 15