Scolari F - Search Results

1

Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci.

Bisceglia L, Cerullo G, Forabosco P, Torres DD, Scolari F, Di Perna M, Foramitti M, Amoroso A, Bertok S, Floege J, Mertens PR, Zerres K, Alexopoulos E, Kirmizis D, Ermelinda M, Zelante L, Schena FP; European IgAN Consortium. Bisceglia L, et al. Among authors: scolari f. Am J Hum Genet. 2006 Dec;79(6):1130-4. doi: 10.1086/510135. Epub 2006 Nov 3. Am J Hum Genet. 2006. PMID: 17186473 Free PMC article.

2

Familial occurrence of primary glomerulonephritis: evidence for a role of genetic factors.

Scolari F, Amoroso A, Savoldi S, Prati E, Scaini P, Manganoni A, Borelli I, Mazzola G, Canale L, Sacchi G, et al. Scolari F, et al. Nephrol Dial Transplant. 1992;7(7):587-96. doi: 10.1093/ndt/7.7.587. Nephrol Dial Transplant. 1992. PMID: 1323067

3

Familial IgM mesangial nephropathy: a morphologic and immunogenetic study of three pedigrees.

Scolari F, Scaini P, Savoldi S, Prati E, Sacchi G, Amoroso A, Mazzola G, Canale L, Borelli I, Cristinelli L, et al. Scolari F, et al. Am J Nephrol. 1990;10(4):261-8. doi: 10.1159/000168118. Am J Nephrol. 1990. PMID: 2240052

4

Familial clustering of IgA nephropathy: further evidence in an Italian population.

Scolari F, Amoroso A, Savoldi S, Mazzola G, Prati E, Valzorio B, Viola BF, Nicola B, Movilli E, Sandrini M, Campanini M, Maiorca R. Scolari F, et al. Am J Kidney Dis. 1999 May;33(5):857-65. doi: 10.1016/s0272-6386(99)70417-8. Am J Kidney Dis. 1999. PMID: 10213640

5

Identification of a new locus for medullary cystic disease, on chromosome 16p12.

Scolari F, Puzzer D, Amoroso A, Caridi G, Ghiggeri GM, Maiorca R, Aridon P, De Fusco M, Ballabio A, Casari G. Scolari F, et al. Am J Hum Genet. 1999 Jun;64(6):1655-60. doi: 10.1086/302414. Am J Hum Genet. 1999. PMID: 10330352 Free PMC article.

6

Familial IgA nephropathy.

Scolari F. Scolari F. J Nephrol. 1999 Jul-Aug;12(4):213-9. J Nephrol. 1999. PMID: 10493564 Review.

7

IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22-23.

Gharavi AG, Yan Y, Scolari F, Schena FP, Frasca GM, Ghiggeri GM, Cooper K, Amoroso A, Viola BF, Battini G, Caridi G, Canova C, Farhi A, Subramanian V, Nelson-Williams C, Woodford S, Julian BA, Wyatt RJ, Lifton RP. Gharavi AG, et al. Among authors: scolari f. Nat Genet. 2000 Nov;26(3):354-7. doi: 10.1038/81677. Nat Genet. 2000. PMID: 11062479

8

Polymorphisms in the promoter region and at codon 54 of the MBL2 gene are not associated with IgA nephropathy.

Pirulli D, Boniotto M, Vatta L, Crovella S, Spano A, Morgutti M, Zezlina S, Bertola L, Roccatello D, Scolari F, Peruzzi L, Savoldi S, Amoroso A. Pirulli D, et al. Among authors: scolari f. Nephrol Dial Transplant. 2001 Apr;16(4):759-64. doi: 10.1093/ndt/16.4.759. Nephrol Dial Transplant. 2001. PMID: 11274270

9

Towards the identification of (a) gene(s) for autosomal dominant medullary cystic kidney disease.

Scolari F, Viola BF, Ghiggeri GM, Caridi G, Amoroso A, Rampoldi L, Casari G. Scolari F, et al. J Nephrol. 2003 May-Jun;16(3):321-8. J Nephrol. 2003. PMID: 12832729 Review.

10

Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics.

Rampoldi L, Caridi G, Santon D, Boaretto F, Bernascone I, Lamorte G, Tardanico R, Dagnino M, Colussi G, Scolari F, Ghiggeri GM, Amoroso A, Casari G. Rampoldi L, et al. Among authors: scolari f. Hum Mol Genet. 2003 Dec 15;12(24):3369-84. doi: 10.1093/hmg/ddg353. Epub 2003 Oct 21. Hum Mol Genet. 2003. PMID: 14570709

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