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西安交通大学 [13]
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期刊论文 [13]
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2019 [2]
2018 [2]
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专题:西安交通大学
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Mutations of ARX and non-syndromic intellectual disability in Chinese population.
期刊论文
Genes & genomics, 2019, 卷号: 41, 页码: 125-131
作者:
Wu Yufei
;
Zhang Huan
;
Liu Xiaofen
;
Shi Zhangyan
;
Li Hongling
收藏
  |  
浏览/下载:23/0
  |  
提交时间:2019/11/19
Genetic counseling
Aristaless-related homeobox (ARX)
Disease-causing mutation
Non-syndromic intellectual disability
Vagus nerve stimulation for pediatric patients with intractable epilepsy between 3 and 6years of age: study protocol for a double-blind, randomized control trial
期刊论文
TRIALS, 2019, 卷号: 20
作者:
Ji, Taoyun
;
Yang, Zhao
;
Liu, Qingzhu
;
Liao, Jianxiang
;
Yin, Fei
收藏
  |  
浏览/下载:36/0
  |  
提交时间:2019/11/19
Vagus nerve stimulation
Pediatric intractable epilepsy
Safety
Efficacy
In-hospital outcomes of dual loading antiplatelet therapy in patients 75 years and older with acute coronary syndrome undergoing percutaneous coronary intervention: Findings from the CCC-ACS (Improving Care for Cardiovascular Disease in China-acute coronary syndrome) project
期刊论文
Journal of the American Heart Association, 2018, 卷号: 7
作者:
Zhao, Guanqi
;
Zhou, Mengge
;
Ma, Changsheng
;
Huo, Yong
;
Smith, Sidney C.
收藏
  |  
浏览/下载:62/0
  |  
提交时间:2019/11/26
Acute coronary syndrome
Antiplatelet therapy
Elderly
Loading dose
Percutaneous coronary intervention
Excavating Anticonvulsant Compounds from Prescriptions of Traditional Chinese Medicine in the Treatment of Epilepsy
期刊论文
AMERICAN JOURNAL OF CHINESE MEDICINE, 2018, 卷号: 46, 页码: 707-737
作者:
Zhao, Zefeng
;
He, Xirui
;
Ma, Cuixia
;
Wu, Shaoping
;
Cuan, Ye
收藏
  |  
浏览/下载:14/0
  |  
提交时间:2019/11/26
Review
Traditional Chinese Medicine
Epilepsy
Anticonvulsant Compounds
A New Role for LOC101928437 in Non-Syndromic Intellectual Disability: Findings from a Family-Based Association Test
期刊论文
PLOS ONE, 2015, 卷号: 10, 期号: [db:dc_citation_issue]
作者:
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  |  
浏览/下载:5/0
  |  
提交时间:2019/12/02
A family-based association study of PRSS12 and mental retardation in the Qinba mountain region of China
期刊论文
PSYCHIATRIC GENETICS, 2013, 卷号: 23, 期号: [db:dc_citation_issue], 页码: 137-137
作者:
Xing, Lianxi
;
Zhang, Kejin
;
Dai, Ling
;
Li, Fengchao
;
Guo, Yale
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2019/12/03
A family-based association study of dopamine receptor D4 and mental retardation in Qinba region of China
期刊论文
NEUROSCIENCE LETTERS, 2012, 卷号: 516, 期号: [db:dc_citation_issue], 页码: 1-4
作者:
Zhang, Kejin
;
Zhang, MeiJie
;
He, Hongjuan
;
Zhang, Jing
;
Chi, Wanyu
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2019/12/10
Family-based association test
Dopamine receptor 4
Mental retardation
A Family-based Association Study of DIO2 and children mental retardation in the Qinba region of China
期刊论文
JOURNAL OF HUMAN GENETICS, 2012, 卷号: 57, 期号: [db:dc_citation_issue], 页码: 14-17
作者:
Zhang, Kejin
;
Xi, Heng
;
Wang, Xiying
;
Guo, Yale
;
Huang, Shaoping
收藏
  |  
浏览/下载:1/0
  |  
提交时间:2019/12/10
Family Based Association Tests (FBAT)
thyroid hormone (TH)
mental retardation (MR)
deiodinase enzyme II (DIO2)
The Genetic variants of IL1RAPL2 gene associated with non-specific mental retardation in Chinese children
期刊论文
International Journal of Genetics and Molecular Biology, 2011, 卷号: 3, 期号: [db:dc_citation_issue], 页码: 149-154
作者:
Kejin, Zhang
;
Bo, He
;
Pingyuan, Gong
;
Xiaocai, Gao
;
Zijian, Zheng
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/10
Association analysis
Genetic variants
Molecular genetics
Non-syndromic mental retardation
Polymorphisms in the DLG3 Gene is not Associated with Non-Syndromic Mental Retardation in the Chinese Han Population of Qin-Ba Mountain
期刊论文
CELLULAR AND MOLECULAR NEUROBIOLOGY, 2011, 卷号: 31, 期号: [db:dc_citation_issue], 页码: 695-700
作者:
Han, Ning
;
Shi, Zhangyan
;
Zhang, Kejin
;
Gao, Xiaocai
;
Zheng, Zijian
收藏
  |  
浏览/下载:1/0
  |  
提交时间:2019/12/10
Discs-large-related 3 (DLG3)
Association study
Non-syndromic mental retardation (NSMR)
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