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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1992 1
1994 1
1995 1
1997 1
1999 2
2001 1
2002 1
2003 2
2004 1
2005 3
2006 2
2008 1
2009 2
2010 3
2011 1
2012 2
2013 1
2015 2
2016 3
2017 1
2018 1
2019 2
2020 2
2021 0
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33 results
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Page 1
Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype.
Noris M, Caprioli J, Bresin E, Mossali C, Pianetti G, Gamba S, Daina E, Fenili C, Castelletti F, Sorosina A, Piras R, Donadelli R, Maranta R, van der Meer I, Conway EM, Zipfel PF, Goodship TH, Remuzzi G. Noris M, et al. Among authors: daina e. Clin J Am Soc Nephrol. 2010 Oct;5(10):1844-59. doi: 10.2215/CJN.02210310. Epub 2010 Jul 1. Clin J Am Soc Nephrol. 2010. PMID: 20595690 Free PMC article.
Rare autoimmune diseases.
Schieppati A, Daina E. Schieppati A, et al. Among authors: daina e. Adv Exp Med Biol. 2010;686:365-74. doi: 10.1007/978-90-481-9485-8_21. Adv Exp Med Biol. 2010. PMID: 20824456 Review.
Improving diagnosis for rare diseases: the experience of the Italian undiagnosed Rare diseases network.
Salvatore M, Polizzi A, De Stefano MC, Floridia G, Baldovino S, Roccatello D, Sciascia S, Menegatti E, Remuzzi G, Daina E, Iatropoulos P, Bembi B, Da Riol RM, Ferlini A, Neri M, Novelli G, Sangiuolo F, Brancati F, Taruscio D. Salvatore M, et al. Among authors: daina e. Ital J Pediatr. 2020 Sep 14;46(1):130. doi: 10.1186/s13052-020-00883-8. Ital J Pediatr. 2020. PMID: 32928283 Free PMC article.
Monogenic diseases that can be cured by liver transplantation.
Fagiuoli S, Daina E, D'Antiga L, Colledan M, Remuzzi G. Fagiuoli S, et al. Among authors: daina e. J Hepatol. 2013 Sep;59(3):595-612. doi: 10.1016/j.jhep.2013.04.004. Epub 2013 Apr 8. J Hepatol. 2013. PMID: 23578885 Free article. Review.
Why rare diseases are an important medical and social issue.
Schieppati A, Henter JI, Daina E, Aperia A. Schieppati A, et al. Among authors: daina e. Lancet. 2008 Jun 14;371(9629):2039-41. doi: 10.1016/S0140-6736(08)60872-7. Lancet. 2008. PMID: 18555915 Review. No abstract available.
C5 Convertase Blockade in Membranoproliferative Glomerulonephritis: A Single-Arm Clinical Trial.
Ruggenenti P, Daina E, Gennarini A, Carrara C, Gamba S, Noris M, Rubis N, Peraro F, Gaspari F, Pasini A, Rigotti A, Lerchner RM, Santoro D, Pisani A, Pasi A, Remuzzi G; EAGLE Study Group. Ruggenenti P, et al. Among authors: daina e. Am J Kidney Dis. 2019 Aug;74(2):224-238. doi: 10.1053/j.ajkd.2018.12.046. Epub 2019 Mar 28. Am J Kidney Dis. 2019. PMID: 30929851
Urinary proteome signature of Renal Cysts and Diabetes syndrome in children.
Ricci P, Magalhães P, Krochmal M, Pejchinovski M, Daina E, Caruso MR, Goea L, Belczacka I, Remuzzi G, Umbhauer M, Drube J, Pape L, Mischak H, Decramer S, Schaefer F, Schanstra JP, Cereghini S, Zürbig P. Ricci P, et al. Among authors: daina e. Sci Rep. 2019 Feb 18;9(1):2225. doi: 10.1038/s41598-019-38713-5. Sci Rep. 2019. PMID: 30778115 Free PMC article.
Outcome of renal transplantation in patients with non-Shiga toxin-associated hemolytic uremic syndrome: prognostic significance of genetic background.
Bresin E, Daina E, Noris M, Castelletti F, Stefanov R, Hill P, Goodship TH, Remuzzi G; International Registry of Recurrent and Familial HUS/TTP. Bresin E, et al. Among authors: daina e. Clin J Am Soc Nephrol. 2006 Jan;1(1):88-99. doi: 10.2215/CJN.00050505. Epub 2005 Nov 2. Clin J Am Soc Nephrol. 2006. PMID: 17699195 Free article. Review.
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