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Page 1
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: carrea a. 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.
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: carrea a. 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
Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis.
Caridi G, Bertelli R, Carrea A, Di Duca M, Catarsi P, Artero M, Carraro M, Zennaro C, Candiano G, Musante L, Seri M, Ginevri F, Perfumo F, Ghiggeri GM. Caridi G, et al. Among authors: carrea a. J Am Soc Nephrol. 2001 Dec;12(12):2742-2746. doi: 10.1681/ASN.V12122742. J Am Soc Nephrol. 2001. PMID: 11729243
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: carrea a. Nephrol Dial Transplant. 2006 Sep;21(9):2452-63. doi: 10.1093/ndt/gfl274. Epub 2006 Jul 5. Nephrol Dial Transplant. 2006. PMID: 16822791
Apolipoprotein E in idiopathic nephrotic syndrome and focal segmental glomerulosclerosis.
Bruschi M, Catarsi P, Candiano G, Rastaldi MP, Musante L, Scolari F, Artero M, Carraro M, Carrea A, Caridi G, Zennaro C, Sanna-Cherchi S, Viola FB, Ferrario F, Perfumo F, Ghiggeri GM. Bruschi M, et al. Among authors: carrea a. Kidney Int. 2003 Feb;63(2):686-95. doi: 10.1046/j.1523-1755.2003.00777.x. Kidney Int. 2003. PMID: 12631135 Free article.
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: carrea a. 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.
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