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科研机构
山东大学 [15]
内容类型
期刊论文 [13]
会议论文 [2]
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2019 [1]
2018 [3]
2017 [1]
2016 [5]
2015 [3]
2014 [1]
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专题:山东大学
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Cochlear implantation in patients with ossified cochleas
期刊论文
AMERICAN JOURNAL OF OTOLARYNGOLOGY, 2019, 卷号: 40, 期号: 2, 页码: 183-186
作者:
Yan, Tao
;
Zong, Fangru
;
Ma, Xiaojie
;
Xu, Xinbo
;
Chen, Weiliang
收藏
  |  
浏览/下载:14/0
  |  
提交时间:2019/12/11
Cochlear ossification
Postmeningitic deafness
Cochlear implant
Clinical outcome
HRCT
MRI
Cochlear implantation in patients with ossified cochleas
期刊论文
American Journal of Otolaryngology - Head and Neck Medicine and Surgery, 2018
作者:
Yan T.
;
Zong F.
;
Ma X.
;
Xu X.
;
Chen W.
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/11
Clinical outcome
Cochlear implant
Cochlear ossification
HRCT
MRI
Postmeningitic deafness
Targeted Next-Generation Sequencing of a Deafness Gene Panel (MiamiOtoGenes) Analysis in Families Unsuitable for Linkage Analysis
期刊论文
BIOMED RESEARCH INTERNATIONAL, 2018
作者:
Shang, Haiqiong
;
Yan, Denise
;
Tayebi, Naeimeh
;
Saeidi, Kolsoum
;
Sahebalzamani, Afsaneh
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/11
Identification of Binding Partners of Deafness-Related Protein PDZD7
期刊论文
NEURAL PLASTICITY, 2018
作者:
Du, Haibo
;
Ren, Rui
;
Chen, Panpan
;
Xu, Zhigang
;
Wang, Yanfei
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/11
Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China
期刊论文
ANNALS OF HUMAN GENETICS, 2017, 卷号: 81, 期号: 6, 页码: 258-266
作者:
Luo, Jianfen
;
Bai, Xiaohui
;
Zhang, Fengguo
;
Xiao, Yun
;
Gu, Lintao
收藏
  |  
浏览/下载:7/0
  |  
提交时间:2019/12/12
China
GJB2
mutation screening
nonsyndromic sensorineural hearing
loss
profound
SLC26A4
Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay
期刊论文
BIOMED RESEARCH INTERNATIONAL, 2016
作者:
Zhang, Fengguo
;
Xiao, Yun
;
Xu, Lei
;
Zhang, Xue
;
Zhang, Guodong
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2019/12/16
Novel compound heterozygous mutations in MYO7A gene associated with autosomal recessive sensorineural hearing loss in a Chinese family
期刊论文
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2016, 卷号: 83, 期号: 4, 页码: 179-185
作者:
Ma, Yalin
;
Xiao, Yun
;
Zhang, Fengguo
;
Han, Yuechen
;
Li, Jianfeng
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/16
Deafness
Autosomal recessive inheritance
MYO7A gene
Mutation
The expression of NLRX1 in C57BL/6 mice cochlear hair cells: Possible relation to aging- and neomycin-induced deafness
期刊论文
NEUROSCIENCE LETTERS, 2016, 卷号: 616, 页码: 138-146
作者:
Yang, Qianqian
;
Sun, Gaoying
;
Cao, Zhixin
;
Yin, Haiyan
;
Qi, Qi
收藏
  |  
浏览/下载:15/0
  |  
提交时间:2019/12/16
Nucleotide-binding domain and leucine-rich-repeat-containing family
member X1
NLRX1
C57BL/6 mice
Hair cells
Apoptosis
GJB2, SLC26A4, and mitochondrial DNA12S rRNA hot-spots in 156 subjects with non-syndromic hearing loss in Tengzhou, China
期刊论文
ACTA OTO-LARYNGOLOGICA, 2016, 卷号: 136, 期号: 8, 页码: 800-805
作者:
Ma, Yalin
;
Xiao, Yun
;
Bai, Xiaohui
;
Zhang, Fengguo
;
Zhang, Daogong
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2019/12/16
Genes testing
SNPscan
mutation spectrum
non-syndromic deafness
Deafness genes in families with non-syndromic hearing loss in Shandong, China: a genetic study
会议论文
Lancet-Chinese-Academy-of-Medical-Sciences (CAMS) Health Summit, OCT 30-31, 2016
作者:
Bai, Xiaohui
;
Xu, Lei
;
Zhang, Fengguo
;
Xiao, Yun
;
Li, Jianfeng
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/31
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