Literature DB >> 25892104

Coexistence of Graves' Disease in a 14-year-old young girl with Gitelman Syndrome.

Bingbing Zha1, Pengxi Zheng2, Jun Liu2, Xinmei Huang2.   

Abstract

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Mesh：

Year:  2015        PMID： 25892104     DOI： 10.1111/cen.12800

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN： 0300-0664            Impact factor:   3.478


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  4 in total

1.  Hypokalemia, hypomagnesemia, hypocalciuria, and recurrent tetany: Gitelman syndrome in a Chinese pedigree and literature review.

Authors:  Ming-Feng Xia; Hua Bian; Hong Liu; Hui-Juan Wu; Zhi-Gang Zhang; Zhi-Qiang Lu; Xin Gao
Journal:  Clin Case Rep       Date:  2017-03-17

Review 2.  Complicated Gitelman syndrome and autoimmune thyroid disease: a case report with a new homozygous mutation in the SLC12A3 gene and literature review.

Authors:  Haiyang Zhou; Xinhuan Liang; Yingfen Qing; Bihui Meng; Jia Zhou; Song Huang; Shurong Lu; Zhenxing Huang; Haiyan Yang; Yan Ma; Zuojie Luo
Journal:  BMC Endocr Disord       Date:  2018-11-08       Impact factor: 2.763

3.  Genetic Analysis of SLC12A3 Gene in Chinese Patients with Gitelman Syndrome.

Authors:  Yanmei Zeng; Ping Li; Shu Fang; Chunyan Wu; Yudan Zhang; Xiaochun Lin; Meiping Guan
Journal:  Med Sci Monit       Date:  2019-08-09

4.  Novel compound heterozygous mutation of SLC12A3 in Gitelman syndrome co-existent with hyperthyroidism: A case report and literature review.

Authors:  Yong-Zhang Qin; Yan-Ming Liu; Yang Wang; Cong You; Long-Nian Li; Xue-Yan Zhou; Wei-Min Lv; Shi-Hua Hong; Li-Xia Xiao
Journal:  World J Clin Cases       Date:  2022-07-26       Impact factor: 1.534
  4 in total

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