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Page 1
Glomerulocystic kidney disease in a family.
Gusmano R, Caridi G, Marini M, Perfumo F, Ghiggeri GM, Piaggio G, Ceccherini I, Seri M. Gusmano R, et al. Among authors: perfumo f. Nephrol Dial Transplant. 2002 May;17(5):813-8. doi: 10.1093/ndt/17.5.813. Nephrol Dial Transplant. 2002. PMID: 11981068
Broadening the spectrum of diseases related to podocin mutations.
Caridi G, Bertelli R, Di Duca M, Dagnino M, Emma F, Onetti Muda A, Scolari F, Miglietti N, Mazzucco G, Murer L, Carrea A, Massella L, Rizzoni G, Perfumo F, Ghiggeri GM. Caridi G, et al. Among authors: perfumo f. J Am Soc Nephrol. 2003 May;14(5):1278-86. doi: 10.1097/01.asn.0000060578.79050.e0. J Am Soc Nephrol. 2003. PMID: 12707396
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: perfumo f. 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.
Familial forms of nephrotic syndrome.
Caridi G, Trivelli A, Sanna-Cherchi S, Perfumo F, Ghiggeri GM. Caridi G, et al. Among authors: perfumo f. Pediatr Nephrol. 2010 Feb;25(2):241-52. doi: 10.1007/s00467-008-1051-3. Epub 2008 Dec 9. Pediatr Nephrol. 2010. PMID: 19066979 Free PMC article. Review.
197 results