Benetti E - Search Results

1

Immature renal structures associated with a novel UMOD sequence variant.

Benetti E, Caridi G, Vella MD, Rampoldi L, Ghiggeri GM, Artifoni L, Murer L. Benetti E, et al. Am J Kidney Dis. 2009 Feb;53(2):327-31. doi: 10.1053/j.ajkd.2008.08.020. Epub 2008 Oct 31. Am J Kidney Dis. 2009. PMID: 18950917

2

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: benetti e. 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

3

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

Murer L, Benetti E, Artifoni L. Murer L, et al. Among authors: benetti e. 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.

4

Renal hypoplasia without optic coloboma associated with PAX2 gene deletion.

Benetti E, Artifoni L, Salviati L, Pinello L, Perrotta S, Zuffardi O, Zacchello G, Murer L. Benetti E, et al. Nephrol Dial Transplant. 2007 Jul;22(7):2076-8. doi: 10.1093/ndt/gfm187. Epub 2007 Apr 1. Nephrol Dial Transplant. 2007. PMID: 17403695 No abstract available.

5

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

Benetti E, Murer L, Bordugo A, Andreetta B, Artifoni L. Benetti E, et al. 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

6

Investigation of intrarenal viral infections in kidney transplant recipients unveils an association between parvovirus B19 and chronic allograft injury.

Barzon L, Murer L, Pacenti M, Biasolo MA, Della Vella M, Benetti E, Zanon GF, Palù G. Barzon L, et al. Among authors: benetti e. J Infect Dis. 2009 Feb 1;199(3):372-80. doi: 10.1086/596053. J Infect Dis. 2009. PMID: 19099488

7

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. Among authors: benetti e. Nephrol Dial Transplant. 2009 Sep;24(9):2931-7. doi: 10.1093/ndt/gfp161. Epub 2009 Apr 6. Nephrol Dial Transplant. 2009. PMID: 19349296

8

A novel WT1 gene mutation in a three-generation family with progressive isolated focal segmental glomerulosclerosis.

Benetti E, Caridi G, Malaventura C, Dagnino M, Leonardi E, Artifoni L, Ghiggeri GM, Tosatto SC, Murer L. Benetti E, et al. Clin J Am Soc Nephrol. 2010 Apr;5(4):698-702. doi: 10.2215/CJN.05670809. Epub 2010 Feb 11. Clin J Am Soc Nephrol. 2010. PMID: 20150449 Free PMC article.

9

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: benetti e. 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

10

Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract.

Gimelli S, Caridi G, Beri S, McCracken K, Bocciardi R, Zordan P, Dagnino M, Fiorio P, Murer L, Benetti E, Zuffardi O, Giorda R, Wells JM, Gimelli G, Ghiggeri GM. Gimelli S, et al. Among authors: benetti e. Hum Mutat. 2010 Dec;31(12):1352-9. doi: 10.1002/humu.21378. Epub 2010 Nov 9. Hum Mutat. 2010. PMID: 20960469 Free PMC article.

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