Pirulli D - Search Results

1

Role of interferon-gamma gene polymorphisms in susceptibility to IgA nephropathy: a family-based association study.

Schena FP, Cerullo G, Torres DD, Scolari F, Foramitti M, Amoroso A, Pirulli D, Floege J, Mertens PR, Zerres K, Alexopoulos E, Kirmizis D, Zelante L, Bisceglia L. Schena FP, et al. Among authors: pirulli d. Eur J Hum Genet. 2006 Apr;14(4):488-96. doi: 10.1038/sj.ejhg.5201591. Eur J Hum Genet. 2006. PMID: 16493441

2

The IgA nephropathy Biobank. An important starting point for the genetic dissection of a complex trait.

Schena FP, Cerullo G, Torres DD, Scolari F, Foramitti M, Amoroso A, Pirulli D, Floege J, Mertens PR, Zerres K, Alexopoulos E, Kirmizis D, Zelante L, Bisceglia L, Ghiggeri GM, Frascà GM; European IgA nephropathy Consortium. Schena FP, et al. Among authors: pirulli d. BMC Nephrol. 2005 Dec 5;6:14. doi: 10.1186/1471-2369-6-14. BMC Nephrol. 2005. PMID: 16329758 Free PMC article.

3

Genetic variant of C1GalT1 contributes to the susceptibility to IgA nephropathy.

Pirulli D, Crovella S, Ulivi S, Zadro C, Bertok S, Rendine S, Scolari F, Foramitti M, Ravani P, Roccatello D, Savoldi S, Cerullo G, Lanzilotta SG, Bisceglia L, Zelante L, Floege J, Alexopoulos E, Kirmizis D, Ghiggeri GM, Frascà G, Schena FP, Amoroso A; European IgAN Consortium. Pirulli D, et al. J Nephrol. 2009 Jan-Feb;22(1):152-9. J Nephrol. 2009. PMID: 19229831

4

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. Nephrol Dial Transplant. 2001 Apr;16(4):759-64. doi: 10.1093/ndt/16.4.759. Nephrol Dial Transplant. 2001. PMID: 11274270

5

Primary hyperoxaluria: genotype-phenotype correlation.

Pirulli D, Marangella M, Amoroso A. Pirulli D, et al. J Nephrol. 2003 Mar-Apr;16(2):297-309. J Nephrol. 2003. PMID: 12768081 Review.

6

Secreted protein acidic and rich in cysteine (SPARC) gene polymorphism association with hepatocellular carcinoma in Italian patients.

Segat L, Milanese M, Pirulli D, Trevisiol C, Lupo F, Salizzoni M, Amoroso A, Crovella S. Segat L, et al. Among authors: pirulli d. J Gastroenterol Hepatol. 2009 Dec;24(12):1840-6. doi: 10.1111/j.1440-1746.2009.06009.x. J Gastroenterol Hepatol. 2009. PMID: 19817957

7

Association of interferon-gamma +874A polymorphism with reduced long-term inflammatory response in haemodialysis patients.

Biolo G, Amoroso A, Savoldi S, Bosutti A, Martone M, Pirulli D, Bianco F, Ulivi S, Bertok S, Artero M, Barazzoni R, Zanetti M, Grassi G, Guarnieri G, Panzetta G. Biolo G, et al. Among authors: pirulli d. Nephrol Dial Transplant. 2006 May;21(5):1317-22. doi: 10.1093/ndt/gfk033. Epub 2006 Jan 12. Nephrol Dial Transplant. 2006. PMID: 16410273

8

Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine: glyoxylate aminotransferase gene.

Pirulli D, Puzzer D, Ferri L, Crovella S, Amoroso A, Ferrettini C, Marangella M, Mazzola G, Florian F. Pirulli D, et al. Hum Genet. 1999 Jun;104(6):523-5. doi: 10.1007/s004390050998. Hum Genet. 1999. PMID: 10453743

9

MBL2 polymorphisms are involved in HIV-1 infection in Brazilian perinatally infected children.

Boniotto M, Braida L, Pirulli D, Arraes L, Amoroso A, Crovella S. Boniotto M, et al. Among authors: pirulli d. AIDS. 2003 Mar 28;17(5):779-80. doi: 10.1097/00002030-200303280-00025. AIDS. 2003. PMID: 12646810 No abstract available.

10

Uromodulin storage diseases: clinical aspects and mechanisms.

Scolari F, Caridi G, Rampoldi L, Tardanico R, Izzi C, Pirulli D, Amoroso A, Casari G, Ghiggeri GM. Scolari F, et al. Among authors: pirulli d. Am J Kidney Dis. 2004 Dec;44(6):987-99. doi: 10.1053/j.ajkd.2004.08.021. Am J Kidney Dis. 2004. PMID: 15558519 Review.

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