161 related articles for article (PubMed ID: 18409531)
1. [Uromodulin mutation and hyperuricemia].
Kudo E; Itakura M
Nihon Rinsho; 2008 Apr; 66(4):778-83. PubMed ID: 18409531
[TBL] [Abstract][Full Text] [Related]
2. [Familial juvenile hyperuricemic nephropathy (FJHN)].
Kudo E; Itakura M
Nihon Rinsho; 2008 Apr; 66(4):683-6. PubMed ID: 18409515
[TBL] [Abstract][Full Text] [Related]
3. The Uromodulin C744G mutation causes MCKD2 and FJHN in children and adults and may be due to a possible founder effect.
Wolf MT; Beck BB; Zaucke F; Kunze A; Misselwitz J; Ruley J; Ronda T; Fischer A; Eifinger F; Licht C; Otto E; Hoppe B; Hildebrandt F
Kidney Int; 2007 Mar; 71(6):574-81. PubMed ID: 17245395
[TBL] [Abstract][Full Text] [Related]
4. Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics.
Rampoldi L; Caridi G; Santon D; Boaretto F; Bernascone I; Lamorte G; Tardanico R; Dagnino M; Colussi G; Scolari F; Ghiggeri GM; Amoroso A; Casari G
Hum Mol Genet; 2003 Dec; 12(24):3369-84. PubMed ID: 14570709
[TBL] [Abstract][Full Text] [Related]
5. A cluster of mutations in the UMOD gene causes familial juvenile hyperuricemic nephropathy with abnormal expression of uromodulin.
Dahan K; Devuyst O; Smaers M; Vertommen D; Loute G; Poux JM; Viron B; Jacquot C; Gagnadoux MF; Chauveau D; Büchler M; Cochat P; Cosyns JP; Mougenot B; Rider MH; Antignac C; Verellen-Dumoulin C; Pirson Y
J Am Soc Nephrol; 2003 Nov; 14(11):2883-93. PubMed ID: 14569098
[TBL] [Abstract][Full Text] [Related]
6. Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy.
Hart TC; Gorry MC; Hart PS; Woodard AS; Shihabi Z; Sandhu J; Shirts B; Xu L; Zhu H; Barmada MM; Bleyer AJ
J Med Genet; 2002 Dec; 39(12):882-92. PubMed ID: 12471200
[TBL] [Abstract][Full Text] [Related]
7. Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndrome.
Vylet'al P; Kublová M; Kalbácová M; Hodanová K; Baresová V; Stibůrková B; Sikora J; Hůlková H; Zivný J; Majewski J; Simmonds A; Fryns JP; Venkat-Raman G; Elleder M; Kmoch S
Kidney Int; 2006 Sep; 70(6):1155-69. PubMed ID: 16883323
[TBL] [Abstract][Full Text] [Related]
8. Familial nephropathy associated with hyperuricemia in Spain: our experience with 3 families harbouring a UMOD mutation.
Puig JG; Prior C; Martínez-Ara J; Torres RJ
Nucleosides Nucleotides Nucleic Acids; 2006; 25(9-11):1295-300. PubMed ID: 17065110
[TBL] [Abstract][Full Text] [Related]
9. Homozygosity for uromodulin disorders: FJHN and MCKD-type 2.
Rezende-Lima W; Parreira KS; García-González M; Riveira E; Banet JF; Lens XM
Kidney Int; 2004 Aug; 66(2):558-63. PubMed ID: 15253706
[TBL] [Abstract][Full Text] [Related]
10. Clinical characterization of a family with a mutation in the uromodulin (Tamm-Horsfall glycoprotein) gene.
Bleyer AJ; Woodard AS; Shihabi Z; Sandhu J; Zhu H; Satko SG; Weller N; Deterding E; McBride D; Gorry MC; Xu L; Ganier D; Hart TC
Kidney Int; 2003 Jul; 64(1):36-42. PubMed ID: 12787393
[TBL] [Abstract][Full Text] [Related]
11. A novel pattern of mutation in uromodulin disorders: autosomal dominant medullary cystic kidney disease type 2, familial juvenile hyperuricemic nephropathy, and autosomal dominant glomerulocystic kidney disease.
Lens XM; Banet JF; Outeda P; Barrio-Lucía V
Am J Kidney Dis; 2005 Jul; 46(1):52-7. PubMed ID: 15983957
[TBL] [Abstract][Full Text] [Related]
12. Hyperuricemia, gout and the kidney.
Gibson T
Curr Opin Rheumatol; 2012 Mar; 24(2):127-31. PubMed ID: 22157498
[TBL] [Abstract][Full Text] [Related]
13. Hereditary hyperuricemia and renal disease.
Cameron JS; Simmonds HA
Semin Nephrol; 2005 Jan; 25(1):9-18. PubMed ID: 15660329
[TBL] [Abstract][Full Text] [Related]
14. [Primary hyperuricemia due to decreased renal uric acid excretion].
Yamauchi T; Ueda T
Nihon Rinsho; 2008 Apr; 66(4):679-81. PubMed ID: 18409514
[TBL] [Abstract][Full Text] [Related]
15. Familial juvenile hyperuricemic nephropathy: detection of mutations in the uromodulin gene in five Japanese families.
Kudo E; Kamatani N; Tezuka O; Taniguchi A; Yamanaka H; Yabe S; Osabe D; Shinohara S; Nomura K; Segawa M; Miyamoto T; Moritani M; Kunika K; Itakura M
Kidney Int; 2004 May; 65(5):1589-97. PubMed ID: 15086896
[TBL] [Abstract][Full Text] [Related]
16. UROMODULIN mutations cause familial juvenile hyperuricemic nephropathy.
Turner JJ; Stacey JM; Harding B; Kotanko P; Lhotta K; Puig JG; Roberts I; Torres RJ; Thakker RV
J Clin Endocrinol Metab; 2003 Mar; 88(3):1398-401. PubMed ID: 12629136
[TBL] [Abstract][Full Text] [Related]
17. Mapping of a new candidate locus for uromodulin-associated kidney disease (UAKD) to chromosome 1q41.
Hodanová K; Majewski J; Kublová M; Vyletal P; Kalbácová M; Stibůrková B; Hůlková H; Chagnon YC; Lanouette CM; Marinaki A; Fryns JP; Venkat-Raman G; Kmoch S
Kidney Int; 2005 Oct; 68(4):1472-82. PubMed ID: 16164624
[TBL] [Abstract][Full Text] [Related]
18. Evidence for a role of uromodulin in chronic kidney disease progression.
Prajczer S; Heidenreich U; Pfaller W; Kotanko P; Lhotta K; Jennings P
Nephrol Dial Transplant; 2010 Jun; 25(6):1896-903. PubMed ID: 20075439
[TBL] [Abstract][Full Text] [Related]
19. Mutations of the Uromodulin gene in MCKD type 2 patients cluster in exon 4, which encodes three EGF-like domains.
Wolf MT; Mucha BE; Attanasio M; Zalewski I; Karle SM; Neumann HP; Rahman N; Bader B; Baldamus CA; Otto E; Witzgall R; Fuchshuber A; Hildebrandt F
Kidney Int; 2003 Nov; 64(5):1580-7. PubMed ID: 14531790
[TBL] [Abstract][Full Text] [Related]
20. Control of renal uric acid excretion and gout.
Taniguchi A; Kamatani N
Curr Opin Rheumatol; 2008 Mar; 20(2):192-7. PubMed ID: 18349750
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
