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Cited by in CrossRef
For: Qin YZ, Liu YM, Wang Y, You C, Li LN, Zhou XY, Lv WM, Hong SH, Xiao LX. Novel compound heterozygous mutation of SLC12A3 in Gitelman syndrome co-existent with hyperthyroidism: A case report and literature review. World J Clin Cases 2022; 10(21): 7483-7494 [PMID: 36158002 DOI: 10.12998/wjcc.v10.i21.7483]
URL: https://www.wjgnet.com/2307-8960/full/v10/i21/7483.htm
Number Citing Articles
1
Oguzhan Koca, Mustafa Tarık Alay, Ahmet Murt, Aysel Kalayci Yigin, Mehmet Seven, Isil Bavunoglu. A novel homozygous SLC12A3 mutation causing Gitelman syndrome with co-existent autoimmune thyroiditis: a case report and review of the literatureCEN Case Reports 2024; 13(5): 330 doi: 10.1007/s13730-023-00845-z
2
Yanfang Luo, Jianru Hao, Zhenzhen Su, Yujuan Huang, Fen Ye, Yanhui Qiu, Zhimin Liu, Yuping Chen, Renjuan Sun, Yuyu Qiu. Prevalence and Related Factors of Hypokalemia in Patients with Acute Ischemic StrokeInternational Journal of General Medicine 2024; : 5697 doi: 10.2147/IJGM.S492025