Artifoni L - Search Results

1

Upper urinary tract infections are associated with RANTES promoter polymorphism.

Centi S, Negrisolo S, Stefanic A, Benetti E, Cassar W, Da Dalt L, Rigamonti W, Zucchetta P, Montini G, Murer L, Artifoni L. Centi S, et al. Among authors: artifoni l. J Pediatr. 2010 Dec;157(6):1038-1040.e1. doi: 10.1016/j.jpeds.2010.08.006. Epub 2010 Sep 24. J Pediatr. 2010. PMID: 20869067

2

PAX2 gene mutations in pediatric and young adult transplant recipients: kidney and urinary tract malformations without ocular anomalies.

Negrisolo S, Benetti E, Centi S, Della Vella M, Ghirardo G, Zanon GF, Murer L, Artifoni L. Negrisolo S, et al. Among authors: artifoni l. Clin Genet. 2011 Dec;80(6):581-5. doi: 10.1111/j.1399-0004.2010.01588.x. Epub 2010 Nov 25. Clin Genet. 2011. PMID: 21108633

3

SIX1 gene: absence of mutations in children with isolated congenital anomalies of kidney and urinary tract.

Negrisolo S, Centi S, Benetti E, Ghirardo G, Della Vella M, Murer L, Artifoni L. Negrisolo S, et al. Among authors: artifoni l. J Nephrol. 2014 Dec;27(6):667-71. doi: 10.1007/s40620-014-0112-x. Epub 2014 Jun 5. J Nephrol. 2014. PMID: 24899122

4

Interleukin-8 and CXCR1 receptor functional polymorphisms and susceptibility to acute pyelonephritis.

Artifoni L, Negrisolo S, Montini G, Zucchetta P, Molinari PP, Cassar W, Destro R, Anglani F, Rigamonti W, Zacchello G, Murer L. Artifoni L, et al. J Urol. 2007 Mar;177(3):1102-6. doi: 10.1016/j.juro.2006.10.037. J Urol. 2007. PMID: 17296422

5

The impact of eNOS, MTR and MTHFR polymorphisms on renal graft survival in children and young adults.

Artifoni L, Benetti E, Centi S, Negrisolo S, Ghiggeri GM, Ginevri F, Ghio L, Edefonti A, Brambilla C, Cagni N, Murer L. Artifoni L, et al. Nephrol Dial Transplant. 2009 Sep;24(9):2931-7. doi: 10.1093/ndt/gfp161. Epub 2009 Apr 6. Nephrol Dial Transplant. 2009. PMID: 19349296

6

Embryology and genetics of primary vesico-ureteric reflux and associated renal dysplasia.

Murer L, Benetti E, Artifoni L. Murer L, et al. Among authors: artifoni l. Pediatr Nephrol. 2007 Jun;22(6):788-97. doi: 10.1007/s00467-006-0390-1. Epub 2007 Jan 10. Pediatr Nephrol. 2007. PMID: 17216254 Free PMC article.

7

Clinical and molecular markers of chronic interstitial nephropathy in congenital unilateral ureteropelvic junction obstruction.

Murer L, Benetti E, Centi S, Della Vella M, Artifoni L, Capizzi A, Zucchetta P, Del Prete D, Carasi C, Montini G, Rigamonti W, Zaccello G. Murer L, et al. Among authors: artifoni l. J Urol. 2006 Dec;176(6 Pt 1):2668-73; discussion 2673. doi: 10.1016/j.juro.2006.08.055. J Urol. 2006. PMID: 17085190

8

Molecular biology and nuclear medicine in pediatric hydronephrosis.

Zucchetta P, Artifoni L, Rigamonti W, Cecchin D, Bui F, Murer L. Zucchetta P, et al. Among authors: artifoni l. Q J Nucl Med Mol Imaging. 2010 Aug;54(4):363-71. Q J Nucl Med Mol Imaging. 2010. PMID: 20823804 Review.

9

mRNA sequencing of a novel NPHS2 intronic mutation in a child with focal and segmental glomerulosclerosis.

Benetti E, Caridi G, Centi S, Vella MD, Ghiggeri GM, Artifoni L, Murer L. Benetti E, et al. Among authors: artifoni l. Saudi J Kidney Dis Transpl. 2014 Jul;25(4):854-7. doi: 10.4103/1319-2442.135180. Saudi J Kidney Dis Transpl. 2014. PMID: 24969201

10

10p12.1 deletion: HDR phenotype without DGS2 features.

Benetti E, Murer L, Bordugo A, Andreetta B, Artifoni L. Benetti E, et al. Among authors: artifoni l. Exp Mol Pathol. 2009 Feb;86(1):74-6. doi: 10.1016/j.yexmp.2008.10.003. Epub 2008 Oct 31. Exp Mol Pathol. 2009. PMID: 19022243

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