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

Year Number of Results
1985 1
1997 1
1999 1
2000 1
2001 2
2003 3
2004 1
2005 1
2006 4
2007 5
2008 2
2009 3
2010 5
2011 3
2012 4
2013 2
2014 2
2015 1
2017 1
2018 1
2019 1
2021 1
2022 0
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40 results
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Page 1
Discrete Changes in Glucose Metabolism Define Aging.
Ravera S, Podestà M, Sabatini F, Dagnino M, Cilloni D, Fiorini S, Barla A, Frassoni F. Ravera S, et al. Among authors: dagnino m. Sci Rep. 2019 Jul 17;9(1):10347. doi: 10.1038/s41598-019-46749-w. Sci Rep. 2019. PMID: 31316102 Free PMC article.
Clonal haematopoiesis is not prevalent in survivors of childhood cancer.
Collord G, Park N, Podestà M, Dagnino M, Cilloni D, Jones D, Varela I, Frassoni F, Vassiliou GS. Collord G, et al. Among authors: dagnino m. Br J Haematol. 2018 May;181(4):537-539. doi: 10.1111/bjh.14630. Epub 2017 Apr 3. Br J Haematol. 2018. PMID: 28369776 Free PMC article. Clinical Trial. No abstract available.
Identification of Biochemical and Molecular Markers of Early Aging in Childhood Cancer Survivors.
Ravera S, Vigliarolo T, Bruno S, Morandi F, Marimpietri D, Sabatini F, Dagnino M, Petretto A, Bartolucci M, Muraca M, Biasin E, Haupt R, Zecca M, Fagioli F, Cilloni D, Podestà M, Frassoni F. Ravera S, et al. Among authors: dagnino m. Cancers (Basel). 2021 Oct 18;13(20):5214. doi: 10.3390/cancers13205214. Cancers (Basel). 2021. PMID: 34680366 Free PMC article.
Mutations in DSTYK and dominant urinary tract malformations.
Sanna-Cherchi S, Sampogna RV, Papeta N, Burgess KE, Nees SN, Perry BJ, Choi M, Bodria M, Liu Y, Weng PL, Lozanovski VJ, Verbitsky M, Lugani F, Sterken R, Paragas N, Caridi G, Carrea A, Dagnino M, Materna-Kiryluk A, Santamaria G, Murtas C, Ristoska-Bojkovska N, Izzi C, Kacak N, Bianco B, Giberti S, Gigante M, Piaggio G, Gesualdo L, Vukic DK, Vukojevic K, Saraga-Babic M, Saraga M, Gucev Z, Allegri L, Latos-Bielenska A, Casu D, State M, Scolari F, Ravazzolo R, Kiryluk K, Al-Awqati Q, D'Agati VD, Drummond IA, Tasic V, Lifton RP, Ghiggeri GM, Gharavi AG. Sanna-Cherchi S, et al. Among authors: dagnino m. N Engl J Med. 2013 Aug 15;369(7):621-9. doi: 10.1056/NEJMoa1214479. Epub 2013 Jul 17. N Engl J Med. 2013. PMID: 23862974 Free PMC article.
Lack of cardiac anomalies in children with NPHS2 mutations.
Caridi G, Dagnino M, Carrea A, Massella L, Amore A, Emma F, Coppo R, Perfumo F, Ghiggeri GM. Caridi G, et al. Among authors: dagnino m. Nephrol Dial Transplant. 2007 May;22(5):1477-9. doi: 10.1093/ndt/gfl833. Epub 2007 Jan 11. Nephrol Dial Transplant. 2007. PMID: 17218332 No abstract available.
Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome.
Sanna-Cherchi S, Burgess KE, Nees SN, Caridi G, Weng PL, Dagnino M, Bodria M, Carrea A, Allegretta MA, Kim HR, Perry BJ, Gigante M, Clark LN, Kisselev S, Cusi D, Gesualdo L, Allegri L, Scolari F, D'Agati V, Shapiro LS, Pecoraro C, Palomero T, Ghiggeri GM, Gharavi AG. Sanna-Cherchi S, et al. Among authors: dagnino m. Kidney Int. 2011 Aug;80(4):389-96. doi: 10.1038/ki.2011.148. Epub 2011 Jun 22. Kidney Int. 2011. PMID: 21697813 Free article.
Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33.
Sanna-Cherchi S, Caridi G, Weng PL, Dagnino M, Seri M, Konka A, Somenzi D, Carrea A, Izzi C, Casu D, Allegri L, Schmidt-Ott KM, Barasch J, Scolari F, Ravazzolo R, Ghiggeri GM, Gharavi AG. Sanna-Cherchi S, et al. Among authors: dagnino m. Am J Hum Genet. 2007 Mar;80(3):539-49. doi: 10.1086/512248. Epub 2007 Jan 26. Am J Hum Genet. 2007. PMID: 17273976 Free PMC article.
Discordant evolution of nephrotic syndrome in mono- and dizygotic twins.
Ghiggeri GM, Dagnino M, Parodi S, Zennaro C, Amoroso A, Pugliese F, Perfumo F. Ghiggeri GM, et al. Among authors: dagnino m. Pediatr Nephrol. 2006 Mar;21(3):419-22. doi: 10.1007/s00467-005-2106-3. Epub 2005 Dec 29. Pediatr Nephrol. 2006. PMID: 16382323
40 results