185 related articles for article (PubMed ID: 37058043)
1. 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]
2. 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]
3. 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]
4. 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]
5. Gitelman syndrome.
Knoers NV; Levtchenko EN
Orphanet J Rare Dis; 2008 Jul; 3():22. PubMed ID: 18667063
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Persistent hypokalemia due to a rare mutation in gitelman's syndrome.
Mamalis D; Stratigou T; Vallianou NG; Ioannidis GG; Apostolou T
Saudi J Kidney Dis Transpl; 2020; 31(1):259-262. PubMed ID: 32129221
[TBL] [Abstract][Full Text] [Related]
8. [Expert consensus for the diagnosis and treatment of patients with Gitelman syndrome].
Gitelman Syndrome Collaborative Study Group
Zhonghua Nei Ke Za Zhi; 2017 Sep; 56(9):712-716. PubMed ID: 28870047
[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. Gitelman syndrome combined with diabetes mellitus: A case report and literature review.
Huang X; Wu M; Mou L; Zhang Y; Jiang J
Medicine (Baltimore); 2023 Dec; 102(50):e36663. PubMed ID: 38115360
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Quadriparesis in an adult--Gitelman syndrome.
Ahmed S; Qayyum M; Farooq F
J Pak Med Assoc; 2011 Feb; 61(2):182-4. PubMed ID: 21375174
[TBL] [Abstract][Full Text] [Related]
14. Gitelman syndrome: A case report.
Chen SY; Jie N
World J Clin Cases; 2022 Jun; 10(17):5893-5898. PubMed ID: 35979117
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. A novel SLC12A3 homozygous c2039delG mutation in Gitelman syndrome with hypocalcemia.
Yang W; Zhao S; Xie Y; Mo Z
BMC Nephrol; 2018 Dec; 19(1):362. PubMed ID: 30558554
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Early onset children's Gitelman syndrome with severe hypokalaemia: a case report.
Chen H; Ma R; Du H; Liu J; Jin L
BMC Pediatr; 2020 Aug; 20(1):366. PubMed ID: 32758191
[TBL] [Abstract][Full Text] [Related]
19. Long-Term Indomethacin Treatment in a Chinese Child with Gitelman Syndrome: Case Report and Literature Review on its Efficacy and Tolerance.
Peng X; Chen C; Tu J; Lin Y; Li H; Geng H
Am J Case Rep; 2023 Dec; 24():e941627. PubMed ID: 38069462
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]