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吉林大学白求恩第一医... [5]
吉林大学白求恩第三医... [5]
内容类型
期刊论文 [10]
发表日期
2018 [4]
2017 [6]
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A case of a novel CACNA1G mutation from a Chinese family with SCA42 A case report and literature review
期刊论文
MEDICINE, 2018, 卷号: 97, 期号: 36
作者:
Li, Xinyuan
;
Zhou, Chunkui
;
Cui, Li
;
Zhu, Lijun
;
Du, Heqian
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2019/12/05
CACNA1G
cerebellar atrophy
hot cross bun sign
SCA42
spinocerebellar ataxia
Efficacy and tolerability of short-term duloxetine treatment in adults with generalized anxiety disorder: A meta-analysis
期刊论文
PLOS ONE, 2018, 卷号: 13, 期号: 3
作者:
Fang, Shaokuan
;
Li, Xinyuan
;
Zhu, Lijun
;
Zhou, Chunkui
;
Liu, Jing
收藏
  |  
浏览/下载:10/0
  |  
提交时间:2019/12/05
Efficacy and tolerability of short-term duloxetine treatment in adults with generalized anxiety disorder: A meta-analysis
期刊论文
PLOS ONE, 2018, 卷号: 13, 期号: 3
作者:
Li, Xinyuan
;
Zhu, Lijun
;
Zhou, Chunkui
;
Liu, Jing
;
Du, Heqian
收藏
  |  
浏览/下载:9/0
  |  
提交时间:2019/12/05
A case of a novel CACNA1G mutation from a Chinese family with SCA42 A case report and literature review
期刊论文
MEDICINE, 2018, 卷号: 97, 期号: 36
作者:
Wang, Chenglin
;
Li, Xinyuan
;
Zhou, Chunkui
;
Cui, Li
;
Zhu, Lijun
收藏
  |  
浏览/下载:7/0
  |  
提交时间:2019/12/05
CACNA1G
cerebellar atrophy
hot cross bun sign
SCA42
spinocerebellar ataxia
A case of hereditary thrombophilia in a Chinese Han patient with both antithrombin deficiency and Factor V Leiden: A case report and literature review
期刊论文
NEUROENDOCRINOLOGY LETTERS, 2017, 卷号: 38, 期号: 7
作者:
Li, Xinyuan
;
Lin, Weihong
;
Zhu, Lijun
;
Wang, Yonghong
;
Liu, Shan
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/05
hereditary thrombophilia
Factor V Leiden
antithrombin deficiency
activated protein C resistance
venous thromboembolism
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy with spinal cord lesion: A case report and literature review
期刊论文
NEUROLOGY ASIA, 2017, 卷号: 22, 期号: 4
作者:
Du, Heqian
;
Li, Xinyuan
;
Meng, Hongmei
;
Lu, Ziwen
;
Zhu, Lijun
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2019/12/05
CADASIL
spinal cord lesion
NOTCH3 gene
A case of hereditary thrombophilia in a Chinese Han patient with both antithrombin deficiency and Factor V Leiden: A case report and literature review
期刊论文
NEUROENDOCRINOLOGY LETTERS, 2017, 卷号: 38, 期号: 7
作者:
Wang, Yonghong
;
Li, Xinyuan
;
Lin, Weihong
;
Zhu, Lijun
;
Liu, Shan
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/05
hereditary thrombophilia
Factor V Leiden
antithrombin deficiency
activated protein C resistance
venous thromboembolism
Hereditary spastic paraplegia with SPG30 mutation: A report from North East China
期刊论文
NEUROLOGY ASIA, 2017, 卷号: 22, 期号: 2
作者:
Zhou, Chunkui
;
Zhu, Lijun
;
Li, Xinyuan
;
Du, Heqian
;
Dong, Shanshan
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/05
Hereditary spastic paraplegia
SPG30
KIF1A
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy with spinal cord lesion: A case report and literature review
期刊论文
NEUROLOGY ASIA, 2017, 卷号: 22, 期号: 4
作者:
Fang, Shaokuan
;
Du, Heqian
;
Li, Xinyuan
;
Meng, Hongmei
;
Lu, Ziwen
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/05
CADASIL
spinal cord lesion
NOTCH3 gene
Hereditary spastic paraplegia with SPG30 mutation: A report from North East China
期刊论文
NEUROLOGY ASIA, 2017, 卷号: 22, 期号: 2
作者:
Zhou, Chunkui
;
Zhu, Lijun
;
Li, Xinyuan
;
Du, Heqian
;
Dong, Shanshan
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/05
Hereditary spastic paraplegia
SPG30
KIF1A
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