Emma F - Search Results

1

COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement.

Diomedi-Camassei F, Di Giandomenico S, Santorelli FM, Caridi G, Piemonte F, Montini G, Ghiggeri GM, Murer L, Barisoni L, Pastore A, Muda AO, Valente ML, Bertini E, Emma F. Diomedi-Camassei F, et al. Among authors: emma f. J Am Soc Nephrol. 2007 Oct;18(10):2773-80. doi: 10.1681/ASN.2006080833. Epub 2007 Sep 12. J Am Soc Nephrol. 2007. PMID: 17855635

2

Acquired glomerulocystic kidney disease following hemolytic uremic syndrome.

Emma F, Muda AO, Rinaldi S, Boldrini R, Bosman C, Rizzoni G. Emma F, et al. Pediatr Nephrol. 2001 Jul;16(7):557-60. doi: 10.1007/s004670100608. Pediatr Nephrol. 2001. PMID: 11465804

3

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: emma f. 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

4

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: emma f. 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

5

Cyclosporine in patients with steroid-resistant nephrotic syndrome: an open-label, nonrandomized, retrospective study.

Ghiggeri GM, Catarsi P, Scolari F, Caridi G, Bertelli R, Carrea A, Sanna-Cherchi S, Emma F, Allegri L, Cancarini G, Rizzoni GF, Perfumo F. Ghiggeri GM, et al. Among authors: emma f. Clin Ther. 2004 Sep;26(9):1411-8. doi: 10.1016/j.clinthera.2004.09.012. Clin Ther. 2004. PMID: 15531003 Clinical Trial.

6

Angiotensin-converting enzyme (ACE) haplotypes and cyclosporine A (CsA) response: a model of the complex relationship between ACE quantitative trait locus and pathological phenotypes.

Catarsi P, Ravazzolo R, Emma F, Fruci D, Finos L, Frau A, Morreale G, Carrea A, Ghiggeri GM. Catarsi P, et al. Among authors: emma f. Hum Mol Genet. 2005 Aug 15;14(16):2357-67. doi: 10.1093/hmg/ddi238. Epub 2005 Jul 7. Hum Mol Genet. 2005. PMID: 16002416

7

"Bartter-like" phenotype in Kearns-Sayre syndrome.

Emma F, Pizzini C, Tessa A, Di Giandomenico S, Onetti-Muda A, Santorelli FM, Bertini E, Rizzoni G. Emma F, et al. Pediatr Nephrol. 2006 Mar;21(3):355-60. doi: 10.1007/s00467-005-2092-5. Epub 2005 Dec 29. Pediatr Nephrol. 2006. PMID: 16382326

8

Impaired activity of the gamma-glutamyl cycle in nephropathic cystinosis fibroblasts.

Mannucci L, Pastore A, Rizzo C, Piemonte F, Rizzoni G, Emma F. Mannucci L, et al. Among authors: emma f. Pediatr Res. 2006 Feb;59(2):332-5. doi: 10.1203/01.pdr.0000196370.57200.da. Pediatr Res. 2006. PMID: 16439602

9

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: emma f. Gene Expr. 2006;13(1):59-66. doi: 10.3727/000000006783991926. Gene Expr. 2006. PMID: 16572591 Free PMC article.

10

Stop codon at arginine 586 is the prevalent nephronopthisis type 1 mutation in Italy.

Caridi G, Dagnino M, Trivelli A, Emma F, Perfumo F, Ghiggeri GM. Caridi G, et al. Among authors: emma f. Nephrol Dial Transplant. 2006 Aug;21(8):2301-3. doi: 10.1093/ndt/gfl277. Epub 2006 Jun 8. Nephrol Dial Transplant. 2006. PMID: 16762963 No abstract available.

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