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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: scolari 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
Major COL4A5 gene rearrangements in patients with juvenile type Alport syndrome.
Renieri A, Galli L, Grillo A, Bruttini M, Neri T, Zanelli P, Rizzoni G, Massella L, Sessa A, Meroni M, Peratoner L, Riegler P, Scolari F, Mileti M, Giani M, Cossu M, Savi M, Ballabio A, De Marchi M. Renieri A, et al. Among authors: scolari f. Am J Med Genet. 1995 Nov 20;59(3):380-5. doi: 10.1002/ajmg.1320590320. Am J Med Genet. 1995. PMID: 8599366
Medullary cystic kidney disease: past and present.
Scolari F, Viola BF, Prati E, Ghiggeri GM, Caridi G, Amoroso A, Casari G, Maiorca R. Scolari F, et al. Contrib Nephrol. 2001;(136):68-78. doi: 10.1159/000060180. Contrib Nephrol. 2001. PMID: 11688405 Review. No abstract available.
Depletion of clusterin in renal diseases causing nephrotic syndrome.
Ghiggeri GM, Bruschi M, Candiano G, Rastaldi MP, Scolari F, Passerini P, Musante L, Pertica N, Caridi G, Ferrario F, Perfumo F, Ponticelli C. Ghiggeri GM, et al. Among authors: scolari f. Kidney Int. 2002 Dec;62(6):2184-94. doi: 10.1046/j.1523-1755.2002.00664.x. Kidney Int. 2002. PMID: 12427144 Free article.
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: scolari f. Kidney Int. 2003 Feb;63(2):686-95. doi: 10.1046/j.1523-1755.2003.00777.x. Kidney Int. 2003. PMID: 12631135 Free article.
371 results