Murer L - Search Results

1

Broadening the spectrum of diseases related to podocin mutations.

Caridi G, Bertelli R, Di Duca M, Dagnino M, Emma F, Onetti Muda A, Scolari F, Miglietti N, Mazzucco G, Murer L, Carrea A, Massella L, Rizzoni G, Perfumo F, Ghiggeri GM. Caridi G, et al. Among authors: murer l. J Am Soc Nephrol. 2003 May;14(5):1278-86. doi: 10.1097/01.asn.0000060578.79050.e0. J Am Soc Nephrol. 2003. PMID: 12707396

2

Immunohistochemical distribution of endothelin in biopsies of pediatric nephrotic syndrome.

Murer L, Zacchello G, Basso G, Scarpa A, Montini G, Chiozza ML, Zacchello F. Murer L, et al. Am J Nephrol. 1994;14(3):157-61. doi: 10.1159/000168707. Am J Nephrol. 1994. PMID: 7977473

3

Renal-retinal syndromes: association of retinal anomalies and recessive nephronophthisis in patients with homozygous deletion of the NPH1 locus.

Caridi G, Murer L, Bellantuono R, Sorino P, Caringella DA, Gusmano R, Ghiggeri GM. Caridi G, et al. Among authors: murer l. Am J Kidney Dis. 1998 Dec;32(6):1059-62. doi: 10.1016/s0272-6386(98)70083-6. Am J Kidney Dis. 1998. PMID: 9856524 Review.

4

Clinical and molecular heterogeneity of juvenile nephronophthisis in Italy: insights from molecular screening.

Caridi G, Dagnino M, Gusmano R, Ginevri F, Murer L, Ghio L, Piaggio G, Ciardi MR, Perfumo F, Ghiggeri GM. Caridi G, et al. Among authors: murer l. Am J Kidney Dis. 2000 Jan;35(1):44-51. doi: 10.1016/S0272-6386(00)70300-3. Am J Kidney Dis. 2000. PMID: 10620543

5

Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin.

Bertelli R, Ginevri F, Caridi G, Dagnino M, Sandrini S, Di Duca M, Emma F, Sanna-Cherchi S, Scolari F, Neri TM, Murer L, Massella L, Basile G, Rizzoni G, Perfumo F, Ghiggeri GM. Bertelli R, et al. Among authors: murer l. Am J Kidney Dis. 2003 Jun;41(6):1314-21. doi: 10.1016/s0272-6386(03)00364-0. Am J Kidney Dis. 2003. PMID: 12776285

6

Mutational spectrum of the CTNS gene in Italy.

Mason S, Pepe G, Dall'Amico R, Tartaglia S, Casciani S, Greco M, Bencivenga P, Murer L, Rizzoni G, Tenconi R, Clementi M. Mason S, et al. Among authors: murer l. Eur J Hum Genet. 2003 Jul;11(7):503-8. doi: 10.1038/sj.ejhg.5200993. Eur J Hum Genet. 2003. PMID: 12825071

7

Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindreds.

Sanna-Cherchi S, Reese A, Hensle T, Caridi G, Izzi C, Kim YY, Konka A, Murer L, Scolari F, Ravazzolo R, Ghiggeri GM, Gharavi AG. Sanna-Cherchi S, et al. Among authors: murer l. J Am Soc Nephrol. 2005 Jun;16(6):1781-7. doi: 10.1681/ASN.2004121034. Epub 2005 Apr 13. J Am Soc Nephrol. 2005. PMID: 15829711 Free article.

8

Rare functional variants of podocin (NPHS2) promoter in patients with nephrotic syndrome.

Oleggini R, Bertelli R, Di Donato A, Di Duca M, Caridi G, Sanna-Cherchi S, Scolari F, Murer L, Allegri L, Coppo R, Emma F, Camussi G, Perfumo F, Ghiggeri GM. Oleggini R, et al. Among authors: murer l. Gene Expr. 2006;13(1):59-66. doi: 10.3727/000000006783991926. Gene Expr. 2006. PMID: 16572591 Free PMC article.

9

Phenotypic and genetic heterogeneity in Dent's disease--the results of an Italian collaborative study.

Tosetto E, Ghiggeri GM, Emma F, Barbano G, Carrea A, Vezzoli G, Torregrossa R, Cara M, Ripanti G, Ammenti A, Peruzzi L, Murer L, Ratsch IM, Citron L, Gambaro G, D'angelo A, Anglani F. Tosetto E, et al. Among authors: murer l. Nephrol Dial Transplant. 2006 Sep;21(9):2452-63. doi: 10.1093/ndt/gfl274. Epub 2006 Jul 5. Nephrol Dial Transplant. 2006. PMID: 16822791

10

Nephronophthisis type 1 deletion syndrome with neurological symptoms: prevalence and significance of the association.

Caridi G, Dagnino M, Rossi A, Valente EM, Bertini E, Fazzi E, Emma F, Murer L, Verrina E, Ghiggeri GM. Caridi G, et al. Among authors: murer l. Kidney Int. 2006 Oct;70(7):1342-7. doi: 10.1038/sj.ki.5001768. Epub 2006 Aug 9. Kidney Int. 2006. PMID: 16900087 Free article.

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