Similar articles for PMID: 21536615

Year	Number of Results
1979	1
1996	2
1997	1
1999	1
2001	2
2002	2
2003	3
2004	3
2005	4
2006	8
2007	3
2008	8
2009	8
2010	5
2011	14
2012	9
2013	9
2014	10
2015	11
2016	9
2017	4
2018	12
2019	12
2020	10
2021	10
2022	9
2023	7
2024	0

1

Recurrent EIARF and PRES with severe renal hypouricemia by compound heterozygous SLC2A9 mutation.

Shima Y, Nozu K, Nozu Y, Togawa H, Kaito H, Matsuo M, Iijima K, Nakanishi K, Yoshikawa N. Shima Y, et al. Pediatrics. 2011 Jun;127(6):e1621-5. doi: 10.1542/peds.2010-2592. Epub 2011 May 2. Pediatrics. 2011. PMID: 21536615

2

A novel homozygous GLUT9 mutation cause recurrent exercise-induced acute renal failure and posterior reversible encephalopathy syndrome.

Mou LJ, Jiang LP, Hu Y. Mou LJ, et al. J Nephrol. 2015 Jun;28(3):387-92. doi: 10.1007/s40620-014-0073-0. Epub 2014 Mar 19. J Nephrol. 2015. PMID: 24643436

3

Recurrent exercise-induced acute renal failure in a young Pakistani man with severe renal hypouricemia and SLC2A9 compound heterozygosity.

Jeannin G, Chiarelli N, Gaggiotti M, Ritelli M, Maiorca P, Quinzani S, Verzeletti F, Possenti S, Colombi M, Cancarini G. Jeannin G, et al. BMC Med Genet. 2014 Jan 7;15:3. doi: 10.1186/1471-2350-15-3. BMC Med Genet. 2014. PMID: 24397858 Free PMC article.

4

Molecular background of urate transporter genes in patients with exercise-induced acute kidney injury.

Kaito H, Ishimori S, Nozu K, Shima Y, Nakanishi K, Yoshikawa N, Iijima K. Kaito H, et al. Am J Nephrol. 2013;38(4):316-20. doi: 10.1159/000355430. Epub 2013 Oct 4. Am J Nephrol. 2013. PMID: 24107611

5

Pathogenic GLUT9 mutations causing renal hypouricemia type 2 (RHUC2).

Kawamura Y, Matsuo H, Chiba T, Nagamori S, Nakayama A, Inoue H, Utsumi Y, Oda T, Nishiyama J, Kanai Y, Shinomiya N. Kawamura Y, et al. Nucleosides Nucleotides Nucleic Acids. 2011 Dec;30(12):1105-11. doi: 10.1080/15257770.2011.623685. Nucleosides Nucleotides Nucleic Acids. 2011. PMID: 22132964

6

Functional analysis of novel allelic variants in URAT1 and GLUT9 causing renal hypouricemia type 1 and 2.

Mancikova A, Krylov V, Hurba O, Sebesta I, Nakamura M, Ichida K, Stiburkova B. Mancikova A, et al. Clin Exp Nephrol. 2016 Aug;20(4):578-584. doi: 10.1007/s10157-015-1186-z. Epub 2015 Oct 24. Clin Exp Nephrol. 2016. PMID: 26500098

7

Diagnostic tests for primary renal hypouricemia.

Sebesta I, Stiburkova B, Bartl J, Ichida K, Hosoyamada M, Taylor J, Marinaki A. Sebesta I, et al. Nucleosides Nucleotides Nucleic Acids. 2011 Dec;30(12):1112-6. doi: 10.1080/15257770.2011.611483. Nucleosides Nucleotides Nucleic Acids. 2011. PMID: 22132965

8

Identification of a hypouricemia patient with SLC2A9 R380W, a pathogenic mutation for renal hypouricemia type 2.

Chiba T, Matsuo H, Nagamori S, Nakayama A, Kawamura Y, Shimizu S, Sakiyama M, Hosoyamada M, Kawai S, Okada R, Hamajima N, Kanai Y, Shinomiya N. Chiba T, et al. Nucleosides Nucleotides Nucleic Acids. 2014;33(4-6):261-5. doi: 10.1080/15257770.2013.857781. Nucleosides Nucleotides Nucleic Acids. 2014. PMID: 24940677

9

Two novel homozygous SLC2A9 mutations cause renal hypouricemia type 2.

Dinour D, Gray NK, Ganon L, Knox AJ, Shalev H, Sela BA, Campbell S, Sawyer L, Shu X, Valsamidou E, Landau D, Wright AF, Holtzman EJ. Dinour D, et al. Nephrol Dial Transplant. 2012 Mar;27(3):1035-41. doi: 10.1093/ndt/gfr419. Epub 2011 Aug 2. Nephrol Dial Transplant. 2012. PMID: 21810765

10

URAT1 mutations cause renal hypouricemia type 1 in Iraqi Jews.

Dinour D, Bahn A, Ganon L, Ron R, Geifman-Holtzman O, Knecht A, Gafter U, Rachamimov R, Sela BA, Burckhardt G, Holtzman EJ. Dinour D, et al. Nephrol Dial Transplant. 2011 Jul;26(7):2175-81. doi: 10.1093/ndt/gfq722. Epub 2010 Dec 9. Nephrol Dial Transplant. 2011. PMID: 21148271

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