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264 results

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Page 1
Clinical and genetic characteristics of Dent's disease type 1 in Europe.
Burballa C, Cantero-Recasens G, Prikhodina L, Lugani F, Schlingmann K, Ananin PV, Besouw M, Bockenhauer D, Madariaga L, Bertholet-Thomas A, Taroni F, Parolin M, Conlon P, Emma F, Del Prete D, Chauveau D, Koster-Kamphuis L, Fila M, Pasini A, Castro I, Colussi G, Gil M, Mohidin B, Wlodkowski T, Schaefer F, Ariceta G; DENT study group. Burballa C, et al. Among authors: emma f. Nephrol Dial Transplant. 2023 May 31;38(6):1497-1507. doi: 10.1093/ndt/gfac310. Nephrol Dial Transplant. 2023. PMID: 36441012
Phenotypic and genetic heterogeneity in Dent's disease--the results of an Italian collaborative study.
Tosetto E, Ghiggeri GM, Emma F, Barbano G, Carrea A, Vezzoli G, Torregrossa R, Cara M, Ripanti G, Ammenti A, Peruzzi L, Murer L, Ratsch IM, Citron L, Gambaro G, D'angelo A, Anglani F. Tosetto E, et al. Among authors: emma f. Nephrol Dial Transplant. 2006 Sep;21(9):2452-63. doi: 10.1093/ndt/gfl274. Epub 2006 Jul 5. Nephrol Dial Transplant. 2006. PMID: 16822791
COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement.
Diomedi-Camassei F, Di Giandomenico S, Santorelli FM, Caridi G, Piemonte F, Montini G, Ghiggeri GM, Murer L, Barisoni L, Pastore A, Muda AO, Valente ML, Bertini E, Emma F. Diomedi-Camassei F, et al. Among authors: emma f. J Am Soc Nephrol. 2007 Oct;18(10):2773-80. doi: 10.1681/ASN.2006080833. Epub 2007 Sep 12. J Am Soc Nephrol. 2007. PMID: 17855635
Genetic risk factors in typical haemolytic uraemic syndrome.
Taranta A, Gianviti A, Palma A, De Luca V, Mannucci L, Procaccino MA, Ghiggeri GM, Caridi G, Fruci D, Ferracuti S, Ferretti A, Pecoraro C, Gaido M, Penza R, Edefonti A, Murer L, Tozzi AE, Emma F. Taranta A, et al. Among authors: emma f. Nephrol Dial Transplant. 2009 Jun;24(6):1851-7. doi: 10.1093/ndt/gfn720. Epub 2008 Dec 25. Nephrol Dial Transplant. 2009. PMID: 19110485
Improvement in the renal prognosis in nephropathic cystinosis.
Van Stralen KJ, Emma F, Jager KJ, Verrina E, Schaefer F, Laube GF, Lewis MA, Levtchenko EN. Van Stralen KJ, et al. Among authors: emma f. Clin J Am Soc Nephrol. 2011 Oct;6(10):2485-91. doi: 10.2215/CJN.02000311. Epub 2011 Aug 25. Clin J Am Soc Nephrol. 2011. PMID: 21868618 Free PMC 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. Among authors: emma f. 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.
Eculizumab for the treatment of dense-deposit disease.
Vivarelli M, Pasini A, Emma F. Vivarelli M, et al. Among authors: emma f. N Engl J Med. 2012 Mar 22;366(12):1163-5. doi: 10.1056/NEJMc1111953. N Engl J Med. 2012. PMID: 22435383 No abstract available.
Lupus nephritis in children and adolescents: results of the Italian Collaborative Study.
Ruggiero B, Vivarelli M, Gianviti A, Benetti E, Peruzzi L, Barbano G, Corona F, Ventura G, Pecoraro C, Murer L, Ghiggeri GM, Pennesi M, Edefonti A, Coppo R, Emma F. Ruggiero B, et al. Among authors: emma f. Nephrol Dial Transplant. 2013 Jun;28(6):1487-96. doi: 10.1093/ndt/gfs589. Epub 2013 Jan 22. Nephrol Dial Transplant. 2013. PMID: 23345627
Genotype-phenotype associations in WT1 glomerulopathy.
Lipska BS, Ranchin B, Iatropoulos P, Gellermann J, Melk A, Ozaltin F, Caridi G, Seeman T, Tory K, Jankauskiene A, Zurowska A, Szczepanska M, Wasilewska A, Harambat J, Trautmann A, Peco-Antic A, Borzecka H, Moczulska A, Saeed B, Bogdanovic R, Kalyoncu M, Simkova E, Erdogan O, Vrljicak K, Teixeira A, Azocar M, Schaefer F; PodoNet Consortium. Lipska BS, et al. Kidney Int. 2014 May;85(5):1169-78. doi: 10.1038/ki.2013.519. Epub 2014 Jan 8. Kidney Int. 2014. PMID: 24402088 Free article.
264 results