629 related articles for article (PubMed ID: 18667063)
1. Gitelman syndrome.
Knoers NV; Levtchenko EN
Orphanet J Rare Dis; 2008 Jul; 3():22. PubMed ID: 18667063
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. 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]
4. Gitelman's syndrome: report of one case.
Chan CF; Mu SC; Lau BH; Chang CJ; Lin SH
Acta Paediatr Taiwan; 2008; 49(1):31-4. PubMed ID: 18581727
[TBL] [Abstract][Full Text] [Related]
5. Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference.
Blanchard A; Bockenhauer D; Bolignano D; Calò LA; Cosyns E; Devuyst O; Ellison DH; Karet Frankl FE; Knoers NV; Konrad M; Lin SH; Vargas-Poussou R
Kidney Int; 2017 Jan; 91(1):24-33. PubMed ID: 28003083
[TBL] [Abstract][Full Text] [Related]
6. Mutations in SLC12A3 and CLCNKB and Their Correlation with Clinical Phenotype in Patients with Gitelman and Gitelman-like Syndrome.
Lee JW; Lee J; Heo NJ; Cheong HI; Han JS
J Korean Med Sci; 2016 Jan; 31(1):47-54. PubMed ID: 26770037
[TBL] [Abstract][Full Text] [Related]
7. Gitelman's syndrome: a pathophysiological and clinical update.
Nakhoul F; Nakhoul N; Dorman E; Berger L; Skorecki K; Magen D
Endocrine; 2012 Feb; 41(1):53-7. PubMed ID: 22169961
[TBL] [Abstract][Full Text] [Related]
8. Intrafamilial phenotype variability in patients with Gitelman syndrome having the same mutations in their thiazide-sensitive sodium/chloride cotransporter.
Lin SH; Cheng NL; Hsu YJ; Halperin ML
Am J Kidney Dis; 2004 Feb; 43(2):304-12. PubMed ID: 14750096
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Novel NCC mutants and functional analysis in a new cohort of patients with Gitelman syndrome.
Glaudemans B; Yntema HG; San-Cristobal P; Schoots J; Pfundt R; Kamsteeg EJ; Bindels RJ; Knoers NV; Hoenderop JG; Hoefsloot LH
Eur J Hum Genet; 2012 Mar; 20(3):263-70. PubMed ID: 22009145
[TBL] [Abstract][Full Text] [Related]
12. Two novel mutations of thiazide-sensitive Na-Cl cotrans porter (TSC) gene in two sporadic Japanese patients with Gitelman syndrome.
Tajima T; Kobayashi Y; Abe S; Takahashi M; Konno M; Nakae J; Okuhara K; Satoh K; Ishikawa T; Imai T; Fujieda K
Endocr J; 2002 Feb; 49(1):91-6. PubMed ID: 12008755
[TBL] [Abstract][Full Text] [Related]
13. Gitelman syndrome with normocalciuria - a case report.
Flisiński M; Skalska E; Mączyńska B; Butt-Hussaim N; Sobczyńska-Tomaszewska A; Haus O; Manitius J
BMC Nephrol; 2022 May; 23(1):170. PubMed ID: 35509038
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Generation and analysis of the thiazide-sensitive Na+ -Cl- cotransporter (Ncc/Slc12a3) Ser707X knockin mouse as a model of Gitelman syndrome.
Yang SS; Lo YF; Yu IS; Lin SW; Chang TH; Hsu YJ; Chao TK; Sytwu HK; Uchida S; Sasaki S; Lin SH
Hum Mutat; 2010 Dec; 31(12):1304-15. PubMed ID: 20848653
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Gitelman's syndrome: towards genotype-phenotype correlations?
Riveira-Munoz E; Chang Q; Bindels RJ; Devuyst O
Pediatr Nephrol; 2007 Mar; 22(3):326-32. PubMed ID: 17061123
[TBL] [Abstract][Full Text] [Related]
19. A novel initial codon mutation of the thiazide-sensitive Na-Cl cotransporter gene in a Japanese patient with Gitelman's syndrome.
Aoki K; Tajima T; Yabushita Y; Nakamura A; Nezu U; Takahashi M; Kimura M; Terauchi Y
Endocr J; 2008 Jul; 55(3):557-60. PubMed ID: 18520105
[TBL] [Abstract][Full Text] [Related]
20. [Gitelman´s syndrome as common cause of hypokalemia and hypomagnesemia].
Ryšavá R; Reiterová J; Urbanová M; Štekrová J; Lněnička P; Tesař V
Vnitr Lek; 2016; 62 Suppl 6():78-83. PubMed ID: 28124936
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]