×
验证码:
换一张
忘记密码?
记住我
CORC
首页
科研机构
检索
知识图谱
申请加入
托管服务
登录
注册
在结果中检索
科研机构
中国医学科学院 北... [16]
四川大学 [3]
山东大学 [3]
中南大学 [2]
复旦大学上海医学院 [2]
上海神经科学研究所 [1]
更多...
内容类型
期刊论文 [28]
会议论文 [3]
发表日期
2019 [2]
2018 [5]
2017 [9]
2016 [5]
2015 [3]
2014 [3]
更多...
学科主题
Genetics &... [1]
×
知识图谱
CORC
开始提交
已提交作品
待认领作品
已认领作品
未提交全文
收藏管理
QQ客服
官方微博
反馈留言
浏览/检索结果:
共31条,第1-10条
帮助
已选(
0
)
清除
条数/页:
5
10
15
20
25
30
35
40
45
50
55
60
65
70
75
80
85
90
95
100
排序方式:
请选择
作者升序
作者降序
题名升序
题名降序
发表日期升序
发表日期降序
提交时间升序
提交时间降序
Characteristics and Follow-Up of 13 pedigrees with Gitelman syndrome
期刊论文
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2019, 卷号: 42, 期号: 6, 页码: 653-665
作者:
Zhong, F.
;
Ying, H.
;
Jia, W.
;
Zhou, X.
;
Zhang, H.
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/11
Gitelman syndrome
Pedigree
Solute carrier family 12
member 3
(SLC12A3)
Genotype
Phenotype
Follow-up
Genetic screening for Bartter syndrome and Gitelman syndrome pathogenic genes among individuals with hypertension and hypokalemia
期刊论文
2019, 卷号: 41, 期号: 4, 页码: 381-388
作者:
Bao, Minghui
;
Cai, Jun
;
Yang, Xinchun
;
Ma, Wenjun
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2020/01/03
Bartter syndrome
Gitelman syndrome
hypertension
hypokalemia
gene
sequencing
Consideration of the diagnosis of hypertension accompanied with hypokalaemia: monism or dualism?
期刊论文
The Journal of international medical research, 2018
作者:
Lü Qingguo
;
Dong Yajie
;
Wan Heng
;
Zhang Yuwei
;
Tang Lizhi
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2019/02/25
Diagnosis
Gitelman syndrome
gene analysis
hypertension
hypokalaemia
Characteristics and Follow-Up of 13 pedigrees with Gitelman syndrome
期刊论文
Journal of Endocrinological Investigation, 2018
作者:
Zhong F.
;
Ying H.
;
Jia W.
;
Zhou X.
;
Zhang H.
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/11
Follow-up
Genotype
Gitelman syndrome
Pedigree
Phenotype
Solute carrier family 12, member 3 (SLC12A3)
Hydrochlorothiazide Test as a Tool in the Diagnosis of Gitelman Syndrome in Chinese Patients
期刊论文
2018, 卷号: 9, 页码: 559
作者:
Peng, Xiaoyan
;
Zhao, Bingbin
;
Zhang, Lei
;
Jiang, Lanping
;
Yuan, Tao
收藏
  |  
浏览/下载:10/0
  |  
提交时间:2020/01/03
Gitelman syndrome
diagnosis
hypomagnesemia
hypocalciuria
hydrochlorothiazide test
GENDER DIFFERENCES OF PHENOTYPE IN GITELMAN SYNDROME, AND THE MANAGEMENT OF PREGNANCY IN THIS DISEASE: A LARGE COHORT OF 105 PATIENTS
会议论文
JOURNAL OF HYPERTENSION, 2018-10-01
作者:
Zhang, Lei
;
Peng, Xiaoyan
;
Zhao, Bingbin
;
Yuan, Tao
;
Wang, Ying
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2020/01/03
NCC
Gitelman syndrome
phenotype
gender difference
pregnancy
GENDER DIFFERENCES OF PHENOTYPE IN GITELMAN SYNDROME, AND THE MANAGEMENT OF PREGNANCY IN THIS DISEASE: A LARGE COHORT OF 105 PATIENTS
期刊论文
2018, 卷号: 36, 页码: E336-E336
作者:
Zhang, Lei
;
Peng, Xiaoyan
;
Zhao, Bingbin
;
Yuan, Tao
;
Wang, Ying
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2020/01/03
NCC
Gitelman syndrome
phenotype
gender difference
pregnancy
Hypokalemia, hypomagnesemia, hypocalciuria, and recurrent tetany: Gitelman syndrome in a Chinese pedigree and literature review
期刊论文
CLINICAL CASE REPORTS, 2017, 卷号: 5, 期号: 5
作者:
Xia, Ming-Feng
;
Bian, Hua
;
Liu, Hong
;
Wu, Hui-Juan
;
Zhang, Zhi-Gang
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2019/12/05
Gitelman syndrome
phenotype-genotype relation
review
SLC12A3
Acquired Gitelman syndrome in a primary Sjogren syndrome patient with a SLC12A3 heterozygous mutation: A case report and literature review
期刊论文
NEPHROLOGY, 2017, 卷号: 22, 期号: 8
作者:
Gu, Xiangchen
;
Su, Zheling
;
Chen, Min
;
Xu, Yanqiu
;
Wang, Yi
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/05
Gitelman's syndrome
Sjogren syndrome
SLC12A3 mutation
sodium-chloride cotransporter
Acquired Gitelman syndrome in a primary Sjögren syndrome patient with a SLC12A3 heterozygous mutation: A case report and literature review
期刊论文
Nephrology (Carlton, Vic.), 2017, 卷号: 22, 页码: 652-655
作者:
Gu Xiangchen[1]
;
Su Zheling[2]
;
Chen Min[3]
;
Xu Yanqiu[4]
;
Wang Yi[5]
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2019/04/26
Gitelman's syndrome
SLC12A3 mutation
Sjögren syndrome
sodium-chloride cotransporter
©版权所有 ©2017 CSpace - Powered by
CSpace