139 related articles for article (PubMed ID: 37906151)
1. [Clinical and genetic analysis of a case of Gitelman syndrome with comorbid Graves disease and adrenocortical adenoma].
Qiao Y; Zhao J; Cao L; Li Y; Wu J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Nov; 40(11):1409-1413. PubMed ID: 37906151
[TBL] [Abstract][Full Text] [Related]
2. Clinical and genetic analysis of a case of Gitelman syndrome accompanied with Graves disease and adrenocortical adenoma: A case report.
Qiao Y; Zhao J; Wu J; Cao L; Song G; Mao J
Medicine (Baltimore); 2024 Apr; 103(15):e37770. PubMed ID: 38608089
[TBL] [Abstract][Full Text] [Related]
3. A NOVEL COMPOUND HETEROZYGOUS VARIANT OF SLC12A3 GENE IN A PEDIGREE WITH GITELMAN SYNDROME CO-EXISTENT WITH THYROID DYSFUNCTION.
Liu S; Ke J; Zhang B; Yu C; Feng Y; Zhao D
Endocr Pract; 2018 Oct; 24(10):889-893. PubMed ID: 30084681
[TBL] [Abstract][Full Text] [Related]
4. Gitelman syndrome with Graves' disease leading to rhabdomyolysis: a case report and literature review.
Xu J; He J; Xu S; Wang R; Peng N; Zhang M
BMC Nephrol; 2023 May; 24(1):123. PubMed ID: 37131142
[TBL] [Abstract][Full Text] [Related]
5. [Genetic analysis of two patients with Gitelman syndrome].
Li Z; Li W; Zhao X; Li L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Mar; 41(3):331-334. PubMed ID: 38448024
[TBL] [Abstract][Full Text] [Related]
6. A novel compound heterozygous variant of the SLC12A3 gene in Gitelman syndrome pedigree.
Chen Y; Zhang Z; Lin X; Pan Q; Zheng F; Li H
BMC Med Genet; 2018 Jan; 19(1):17. PubMed ID: 29378538
[TBL] [Abstract][Full Text] [Related]
7. Genetic Analysis of Gitelman Syndrome: Co-existence with Hyperthyroidism in a Two-year-old Boy.
Yu S; Wang C
Endocr Metab Immune Disord Drug Targets; 2021; 21(8):1524-1530. PubMed ID: 33121425
[TBL] [Abstract][Full Text] [Related]
8. Digenetic inheritance of SLC12A3 and CLCNKB genes in a Chinese girl with Gitelman syndrome.
Kong Y; Xu K; Yuan K; Zhu J; Gu W; Liang L; Wang C
BMC Pediatr; 2019 Apr; 19(1):114. PubMed ID: 30999883
[TBL] [Abstract][Full Text] [Related]
9. Identification of compound mutations of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome exhibiting Bartter syndrome-liked phenotypes.
Dong B; Chen Y; Liu X; Wang Y; Wang F; Zhao Y; Sun X; Zhao W
BMC Nephrol; 2020 Aug; 21(1):328. PubMed ID: 32758178
[TBL] [Abstract][Full Text] [Related]
10. A case of hypokalemia and proteinuria with a new mutation in the SLC12A3 Gene.
Chen Q; Wu Y; Zhao J; Jia Y; Wang W
BMC Nephrol; 2018 Oct; 19(1):275. PubMed ID: 30340552
[TBL] [Abstract][Full Text] [Related]
11. A novel compound heterozygous mutation of SLC12A3 gene in a pedigree with Gitelman syndrome and literature review.
Yang M; Dong Y; Tian J; Yan L; Chen Y; Qiu H; Liu W; Hu Y
Genes Genomics; 2020 Sep; 42(9):1035-1040. PubMed ID: 32712837
[TBL] [Abstract][Full Text] [Related]
12. Novel SLC12A3 gene mutations and clinical characteristics in two pedigrees with Gitelman syndrome.
Ying Q; Ye Z; Zhang W; Pan Y; Dai L; Lin K; Feng X; Dong X; He F
Clin Endocrinol (Oxf); 2023 Nov; 99(5):474-480. PubMed ID: 36562655
[TBL] [Abstract][Full Text] [Related]
13. Whole-exome sequencing in diagnosing 2 cases of Gitelman syndrome.
Xie R; Jin P; Yang Y; Zhang Q; Xiong J
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2022 Mar; 47(3):401-406. PubMed ID: 35545335
[TBL] [Abstract][Full Text] [Related]
14. Multi-centre study of the clinical features and gene variant spectrum of Gitelman syndrome in Chinese children.
Shen Q; Chen J; Yu M; Lin Z; Nan X; Dong B; Fang X; Chen J; Ding G; Zhang A; Gao C; Miao L; Xu Y; Jiang X; Bai H; Zhuang J; Gao X; Xu H;
Clin Genet; 2021 Apr; 99(4):558-564. PubMed ID: 33382082
[TBL] [Abstract][Full Text] [Related]
15. [Genetic analysis of a Chinese pedigree with Cohen syndrome due to compound heterozygous variants of VPS13B gene].
Zhang W; Qi N; Guo L; Wang H; Gao Y; Hou Q; Lou G
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Aug; 40(8):966-972. PubMed ID: 37532496
[TBL] [Abstract][Full Text] [Related]
16. Type 2 diabetes mellitus caused by Gitelman syndrome-related hypokalemia: A case report.
He G; Gang X; Sun Z; Wang P; Wang G; Guo W
Medicine (Baltimore); 2020 Jul; 99(29):e21123. PubMed ID: 32702863
[TBL] [Abstract][Full Text] [Related]
17. [Identification of pathological variants of SLC12A3 gene in a pedigree affected with Gitelman syndrome].
Ma Q; Wu J; Che L; Kong X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Dec; 37(12):1368-1370. PubMed ID: 33306824
[TBL] [Abstract][Full Text] [Related]
18. [Genetic analysis of a Chinese pedigree affected with Mucopolysaccharidosis type ⅢA].
Zuo H; Li Y; Cui Y; Zhang J; Shen C; Zhu W; Du C
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Apr; 40(4):452-457. PubMed ID: 36972941
[TBL] [Abstract][Full Text] [Related]
19. Gitelman syndrome with a novel frameshift variant in SLC12A3 gene accompanied by chronic kidney disease and type 2 diabetes mellitus.
Iio K; Mori T; Bessho S; Imai Y; Hatanaka M; Omori H; Kouhara H; Chiga M; Sohara E; Uchida S; Kaimori JY
CEN Case Rep; 2022 May; 11(2):191-195. PubMed ID: 34617250
[TBL] [Abstract][Full Text] [Related]
20. [Genetic analysis of a child patient with rare fibrochondrogenesis due to COL11A1 gene variant].
Li D; Zhang C; Zhou B; Chen X; Wang Y; Hui L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Apr; 40(4):468-472. PubMed ID: 36972944
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
