152 related articles for article (PubMed ID: 38608089)
1. 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]
2. [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]
3. A case report of Gitelman syndrome in children.
Ying J; Wu H; Zhang R; Wu P; Sui F; Li Z
Medicine (Baltimore); 2023 Apr; 102(15):e33509. PubMed ID: 37058043
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Case report: Gitelman syndrome with diabetes: Confirmed by both hydrochlorothiazide test and genetic testing.
Yang L; Fan J; Liu Y; Ren Y; Liu Z; Fu H; Qi H; Yang J
Medicine (Baltimore); 2023 Jun; 102(24):e33959. PubMed ID: 37327293
[TBL] [Abstract][Full Text] [Related]
7. Complicated Gitelman syndrome and autoimmune thyroid disease: a case report with a new homozygous mutation in the SLC12A3 gene and literature review.
Zhou H; Liang X; Qing Y; Meng B; Zhou J; Huang S; Lu S; Huang Z; Yang H; Ma Y; Luo Z
BMC Endocr Disord; 2018 Nov; 18(1):82. PubMed ID: 30409157
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Novel heterozygous mutations of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome: A care-compliant case report.
Bi Y; Kuang MY; Li ML
Medicine (Baltimore); 2023 Sep; 102(35):e34967. PubMed ID: 37657006
[TBL] [Abstract][Full Text] [Related]
10. Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous
Zhang JH; Ruan DD; Hu YN; Ruan XL; Zhu YB; Yang X; Wu JB; Lin XF; Luo JW; Tang FQ
Biomed Res Int; 2021; 2021():9973161. PubMed ID: 34046503
[TBL] [Abstract][Full Text] [Related]
11. A case of Gitelman syndrome with membranous nephropathy.
Guo X; Yu S; Sun J; Mou L
BMC Nephrol; 2022 Jul; 23(1):267. PubMed ID: 35883046
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. Gitelman syndrome as a cause of psychomotor retardation in a toddler.
Skalova S; Neuman D; Lnenicka P; Stekrova J
Arab J Nephrol Transplant; 2013 Jan; 6(1):37-9. PubMed ID: 23282232
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Gitelman syndrome.
Knoers NV; Levtchenko EN
Orphanet J Rare Dis; 2008 Jul; 3():22. PubMed ID: 18667063
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Gitelman syndrome combined with growth hormone deficiency: Three cases report.
Huang K; Dai YL; Zhang JW; Zhang L; Wu W; Dong GP; Ullah R; Fei Y; Fu JF
Medicine (Baltimore); 2019 Oct; 98(40):e17244. PubMed ID: 31577716
[TBL] [Abstract][Full Text] [Related]
20. Gitelman syndrome in a South African family presenting with hypokalaemia and unusual food cravings.
van der Merwe PD; Rensburg MA; Haylett WL; Bardien S; Davids MR
BMC Nephrol; 2017 Jan; 18(1):38. PubMed ID: 28125972
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]