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Page 1
Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood.
Faguer S, Decramer S, Chassaing N, Bellanné-Chantelot C, Calvas P, Beaufils S, Bessenay L, Lengelé JP, Dahan K, Ronco P, Devuyst O, Chauveau D. Faguer S, et al. Among authors: devuyst o. Kidney Int. 2011 Oct;80(7):768-76. doi: 10.1038/ki.2011.225. Epub 2011 Jul 20. Kidney Int. 2011. PMID: 21775974 Free article.
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. Dahan K, et al. Among authors: devuyst o. J Am Soc Nephrol. 2003 Nov;14(11):2883-93. doi: 10.1097/01.asn.0000092147.83480.b5. J Am Soc Nephrol. 2003. PMID: 14569098
Periodic paralyses: when channels go wrong.
Lengelé JP, Belge H, Devuyst O. Lengelé JP, et al. Among authors: devuyst o. Nephrol Dial Transplant. 2008 Apr;23(4):1098-101. doi: 10.1093/ndt/gfn011. Epub 2008 Feb 16. Nephrol Dial Transplant. 2008. PMID: 18281721 No abstract available.
Expression of renal cystic genes in patients with HNF1B mutations.
Faguer S, Decramer S, Devuyst O, Lengelé JP, Fournié GJ, Chauveau D. Faguer S, et al. Among authors: devuyst o. Nephron Clin Pract. 2012;120(2):c71-8. doi: 10.1159/000334954. Epub 2012 Jan 21. Nephron Clin Pract. 2012. PMID: 22269832 Free article.
The ERA-EDTA Working Group on inherited kidney disorders.
Devuyst O, Antignac C, Bindels RJ, Chauveau D, Emma F, Gansevoort R, Maxwell PH, Ong AC, Remuzzi G, Ronco P, Schaefer F. Devuyst O, et al. Nephrol Dial Transplant. 2012 Jan;27(1):67-9. doi: 10.1093/ndt/gfr764. Nephrol Dial Transplant. 2012. PMID: 22287704 Free article. No abstract available.
Rare inherited kidney diseases: challenges, opportunities, and perspectives.
Devuyst O, Knoers NV, Remuzzi G, Schaefer F; Board of the Working Group for Inherited Kidney Diseases of the European Renal Association and European Dialysis and Transplant Association. Devuyst O, et al. Lancet. 2014 May 24;383(9931):1844-59. doi: 10.1016/S0140-6736(14)60659-0. Lancet. 2014. PMID: 24856029 Free PMC article. Review.
Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management--A KDIGO consensus report.
Eckardt KU, Alper SL, Antignac C, Bleyer AJ, Chauveau D, Dahan K, Deltas C, Hosking A, Kmoch S, Rampoldi L, Wiesener M, Wolf MT, Devuyst O; Kidney Disease: Improving Global Outcomes. Eckardt KU, et al. Among authors: devuyst o. Kidney Int. 2015 Oct;88(4):676-83. doi: 10.1038/ki.2015.28. Epub 2015 Mar 4. Kidney Int. 2015. PMID: 25738250 Free article.
467 results