Showing results (1-10 of 71) with videos related to
Sort By:
Pageof 8
Lin Chuang Er Bi Yan Hou Ke Za Zhi = Journal of Clinical Otorhinolaryngology|June 9, 2005
[Mutation analysis of gene CX31.1 in the hereditary hearing loss pedigrees]Yong Feng, Chufeng He, Kun Xia, et al.Lin Chuang Er Bi Yan Hou Ke Za Zhi = Journal of Clinical Otorhinolaryngology|September 20, 2006
[The application of 3D reconstruction of CT scans for the observation of the cochlear implanted electrode location]Hanbo Liu, Yong Feng, Dengming Chen, et al.Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|September 17, 2010
[An investigation of SLC26A4 gene mutation in nonsydromic hearing impairment in Hunan province of China]Lu Jiang, Yong Feng, Hongsheng Chen, et al.Lin Chuang Er Bi Yan Hou Ke Za Zhi = Journal of Clinical Otorhinolaryngology|September 20, 2006
[The prenatal diagnosis and early intervention of nonsyndromic hearing loss of connexin26 gene]Chufeng He, Yong Feng, Kun Xia, et al.European Journal of Pharmacology|September 15, 2024
Asperuloside activates hepatic NRF2 signaling to stimulate mitochondrial metabolism and restore lipid homeostasis in high fat diet-induced MAFLDChufeng He, Qile Zhang, Ruiwen Zhu, et al.Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|October 15, 2010
[Inhibition of the expression of VEGF gene in nasopharyngeal carcinoma cells by microRNA]Xinzhang Cai, Wei Wei, Suping Zhao, et al.Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|November 25, 2015
[Clinical analysis of Mondini dysplasia with cerebrospinal fluid leakage and preliminary genetic research of it]Lili Wang, Yong Feng, Zhijie Niu, et al.Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|August 4, 2011
[Study of the anatomy related to cochlear implantation guided by HRCT]Xuebin He, Yong Feng, Dengming Chen, et al.Gene|November 14, 2024
A novel frameshift mutation in the DIAPH1 gene causes a Chinese family autosomal dominant nonsyndromic hearing loss: Mutation in DIAPH1 causes hearing lossQi Feng, Lu Jiang, Shuai Zhang, et al.Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|July 27, 2007
[Surgical approaches and related microsurgical anatomy about suprameatal approach: new surgical approach for cochlear implantation]Hanbo Liu, Yong Feng, Dengming Chen, et al.Pageof 8