Negrisolo S - Search Results

1

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

2

Small intestinal submucosa-derived extracellular matrix as a heterotopic scaffold for cardiovascular applications.

Palmosi T, Tolomeo AM, Cirillo C, Sandrin D, Sciro M, Negrisolo S, Todesco M, Caicci F, Santoro M, Dal Lago E, Marchesan M, Modesti M, Bagno A, Romanato F, Grumati P, Fabozzo A, Gerosa G. Palmosi T, et al. Among authors: negrisolo s. Front Bioeng Biotechnol. 2022 Dec 12;10:1042434. doi: 10.3389/fbioe.2022.1042434. eCollection 2022. Front Bioeng Biotechnol. 2022. PMID: 36578513 Free PMC article.

3

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. Among authors: negrisolo s. J Urol. 2007 Mar;177(3):1102-6. doi: 10.1016/j.juro.2006.10.037. J Urol. 2007. PMID: 17296422

4

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: negrisolo s. 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

5

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. 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

6

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. J Nephrol. 2014 Dec;27(6):667-71. doi: 10.1007/s40620-014-0112-x. Epub 2014 Jun 5. J Nephrol. 2014. PMID: 24899122

7

Updated genetic testing of Italian patients referred with a clinical diagnosis of primary hyperoxaluria.

Pelle A, Cuccurullo A, Mancini C, Sebastiano R, Stallone G, Negrisolo S, Benetti E, Peruzzi L, Petrarulo M, De Marchi M, Marangella M, Amoroso A, Giachino D, Mandrile G. Pelle A, et al. Among authors: negrisolo s. J Nephrol. 2017 Apr;30(2):219-225. doi: 10.1007/s40620-016-0287-4. Epub 2016 Mar 5. J Nephrol. 2017. PMID: 26946417 Free article.

8

Deciphering Variability of PKD1 and PKD2 in an Italian Cohort of 643 Patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD).

Carrera P, Calzavara S, Magistroni R, den Dunnen JT, Rigo F, Stenirri S, Testa F, Messa P, Cerutti R, Scolari F, Izzi C, Edefonti A, Negrisolo S, Benetti E, Alibrandi MT, Manunta P, Boletta A, Ferrari M. Carrera P, et al. Among authors: negrisolo s. Sci Rep. 2016 Aug 8;6:30850. doi: 10.1038/srep30850. Sci Rep. 2016. PMID: 27499327 Free PMC article.

9

Could the interaction between LMX1B and PAX2 influence the severity of renal symptoms?

Negrisolo S, Carraro A, Fregonese G, Benetti E, Schaefer F, Alberti M, Melchionda S, Fischetto R, Giordano M, Murer L. Negrisolo S, et al. Eur J Hum Genet. 2018 Nov;26(11):1708-1712. doi: 10.1038/s41431-018-0213-4. Epub 2018 Jul 4. Eur J Hum Genet. 2018. PMID: 29973660 Free PMC article.

10

PAX2 and CAKUT Phenotypes: Report on Two New Variants and a Review of Mutations from the Leiden Open Variation Database.

Negrisolo S, Benetti E. Negrisolo S, et al. Int J Mol Sci. 2023 Feb 19;24(4):4165. doi: 10.3390/ijms24044165. Int J Mol Sci. 2023. PMID: 36835576 Free PMC article.

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