266 related articles for article (PubMed ID: 15610225)
1. A novel missense mutation in SLC5A2 encoding SGLT2 underlies autosomal-recessive renal glucosuria and aminoaciduria.
Magen D; Sprecher E; Zelikovic I; Skorecki K
Kidney Int; 2005 Jan; 67(1):34-41. PubMed ID: 15610225
[TBL] [Abstract][Full Text] [Related]
2. Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2).
van den Heuvel LP; Assink K; Willemsen M; Monnens L
Hum Genet; 2002 Dec; 111(6):544-7. PubMed ID: 12436245
[TBL] [Abstract][Full Text] [Related]
3. Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletion.
Calado J; Sznajer Y; Metzger D; Rita A; Hogan MC; Kattamis A; Scharf M; Tasic V; Greil J; Brinkert F; Kemper MJ; Santer R
Nephrol Dial Transplant; 2008 Dec; 23(12):3874-9. PubMed ID: 18622023
[TBL] [Abstract][Full Text] [Related]
4. Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria.
Calado J; Soto K; Clemente C; Correia P; Rueff J
Hum Genet; 2004 Feb; 114(3):314-6. PubMed ID: 14614622
[TBL] [Abstract][Full Text] [Related]
5. Genetic analysis and literature review of Chinese patients with familial renal glucosuria: Identification of a novel SLC5A2 mutation.
Wang X; Yu M; Wang T; Zhang H; Ping F; Zhang Q; Xu J; Feng K; Xiao X
Clin Chim Acta; 2017 Jun; 469():105-110. PubMed ID: 28365451
[TBL] [Abstract][Full Text] [Related]
6. SLC5A2 mutations, including two novel mutations, responsible for renal glucosuria in Chinese families.
Yu L; Wu M; Hou P; Zhang H
BMC Nephrol; 2020 Feb; 21(1):69. PubMed ID: 32111189
[TBL] [Abstract][Full Text] [Related]
7. Familial renal glucosuria: SLC5A2 mutation analysis and evidence of salt-wasting.
Calado J; Loeffler J; Sakallioglu O; Gok F; Lhotta K; Barata J; Rueff J
Kidney Int; 2006 Mar; 69(5):852-5. PubMed ID: 16518345
[TBL] [Abstract][Full Text] [Related]
8. Decreased expression and function of sodium-glucose co-transporter 2 from a novel C-terminal mutation: a case report.
Yu L; Xu Q; Hou P; Zhang H
BMC Nephrol; 2016 Mar; 17():31. PubMed ID: 27000029
[TBL] [Abstract][Full Text] [Related]
9. Novel SLC5A2 variants contribute to renal glucosuria in Chinese families: abnormal expression and dysfunction of variant SLC5A2.
Yu L; Hou P; Lv JC; Liu GP; Zhang H
Hum Mutat; 2015 Jan; 36(1):79-86. PubMed ID: 25339128
[TBL] [Abstract][Full Text] [Related]
10. A novel compound heterozygous mutation in SLC5A2 contributes to familial renal glucosuria in a Chinese family, and a review of the relevant literature.
Li S; Yang Y; Huang L; Kong M; Yang Z
Mol Med Rep; 2019 May; 19(5):4364-4376. PubMed ID: 30942416
[TBL] [Abstract][Full Text] [Related]
11. Determination of the renal threshold for glucose excretion in Familial Renal Glucosuria.
Aires I; Fila M; Polidori D; Santos AR; Costa AB; Calado J
Nephron; 2015; 129(4):300-4. PubMed ID: 25896487
[TBL] [Abstract][Full Text] [Related]
12. Abnormal expression and dysfunction of novel SGLT2 mutations identified in familial renal glucosuria patients.
Yu L; Lv JC; Zhou XJ; Zhu L; Hou P; Zhang H
Hum Genet; 2011 Mar; 129(3):335-44. PubMed ID: 21165652
[TBL] [Abstract][Full Text] [Related]
13. Genetic and clinical characterization of familial renal glucosuria.
Xu L; Zhao R; Zhao Y; Tang X; Si N; Guo X; Yue C; Nie M; Chen L
Clin Kidney J; 2024 Feb; 17(2):sfad265. PubMed ID: 38344682
[TBL] [Abstract][Full Text] [Related]
14. Familial renal glucosuria: a clinicogenetic study of 23 additional cases.
Lee H; Han KH; Park HW; Shin JI; Kim CJ; Namgung MK; Kim KH; Koo JW; Chung WY; Lee DY; Kim SY; Cheong HI
Pediatr Nephrol; 2012 Jul; 27(7):1091-5. PubMed ID: 22314875
[TBL] [Abstract][Full Text] [Related]
15. Renal glucosuria due to SGLT2 mutations.
Kleta R; Stuart C; Gill FA; Gahl WA
Mol Genet Metab; 2004 May; 82(1):56-8. PubMed ID: 15110322
[TBL] [Abstract][Full Text] [Related]
16. Identification of ten novel SLC5A2 mutations and determination of the renal threshold for glucose excretion in Chinese patients with familial renal glucosuria.
Wang S; Zhao X; Zhang R; Wang C; Han Y; Shao L
Clin Chim Acta; 2019 Mar; 490():102-106. PubMed ID: 30593819
[TBL] [Abstract][Full Text] [Related]
17. Molecular analysis of the SGLT2 gene in patients with renal glucosuria.
Santer R; Kinner M; Lassen CL; Schneppenheim R; Eggert P; Bald M; Brodehl J; Daschner M; Ehrich JH; Kemper M; Li Volti S; Neuhaus T; Skovby F; Swift PG; Schaub J; Klaerke D
J Am Soc Nephrol; 2003 Nov; 14(11):2873-82. PubMed ID: 14569097
[TBL] [Abstract][Full Text] [Related]
18. Influence of Familial Renal Glycosuria Due to Mutations in the SLC5A2 Gene on Changes in Glucose Tolerance over Time.
Ottosson-Laakso E; Tuomi T; Forsén B; Gullström M; Groop PH; Groop L; Vikman P
PLoS One; 2016; 11(1):e0146114. PubMed ID: 26735923
[TBL] [Abstract][Full Text] [Related]
19. Familial Renal Glucosuria Presenting as Paroxysmal Glucosuria and Hypercalciuria Due to a Novel
Van Lerberghe R; Mahieu E; Vanuytsel J; Vanhaute K; Vanfraechem C; Claeys L
Eur J Case Rep Intern Med; 2023; 10(12):004157. PubMed ID: 38077699
[TBL] [Abstract][Full Text] [Related]
20. Effect of kidney disease on glucose handling (including genetic defects).
Calado J; Santer R; Rueff J
Kidney Int Suppl; 2011 Mar; (120):S7-13. PubMed ID: 21358700
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
