Caridi G - Search Results

1

Analbuminemia produced by a novel splicing mutation.

Dolcini L, Caridi G, Dagnino M, Sala A, Gökçe S, Sökücü S, Campagnoli M, Galliano M, Minchiotti L. Dolcini L, et al. Among authors: caridi g. Clin Chem. 2007 Aug;53(8):1549-52. doi: 10.1373/clinchem.2007.089748. Clin Chem. 2007. PMID: 17644793

2

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. 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

3

Juvenile nephronophthisis and related variants: clinical features and molecular approach.

Caridi G, Dagnino M, Miglietti N, Carrea A, Perfumo F, Gusmano R, Ghiggeri GM. Caridi G, et al. Contrib Nephrol. 2001;(136):57-67. doi: 10.1159/000060179. Contrib Nephrol. 2001. PMID: 11688404 Review. No abstract available.

4

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. 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

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: caridi g. 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

Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics.

Rampoldi L, Caridi G, Santon D, Boaretto F, Bernascone I, Lamorte G, Tardanico R, Dagnino M, Colussi G, Scolari F, Ghiggeri GM, Amoroso A, Casari G. Rampoldi L, et al. Among authors: caridi g. Hum Mol Genet. 2003 Dec 15;12(24):3369-84. doi: 10.1093/hmg/ddg353. Epub 2003 Oct 21. Hum Mol Genet. 2003. PMID: 14570709

7

Infantile steroid-resistant nephrotic syndrome associated with double homozygous mutations of podocin.

Caridi G, Berdeli A, Dagnino M, Di Duca M, Mir S, Cura A, Ravazzolo R, Ghiggeri GM. Caridi G, et al. Am J Kidney Dis. 2004 Apr;43(4):727-32. doi: 10.1053/j.ajkd.2003.12.034. Am J Kidney Dis. 2004. PMID: 15042551

8

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. 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.

9

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. 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.

10

crv4, a mouse model for human ataxia associated with kyphoscoliosis caused by an mRNA splicing mutation of the metabotropic glutamate receptor 1 (Grm1).

Conti V, Aghaie A, Cilli M, Martin N, Caridi G, Musante L, Candiano G, Castagna M, Fairen A, Ravazzolo R, Guenet JL, Puliti A. Conti V, et al. Among authors: caridi g. Int J Mol Med. 2006 Oct;18(4):593-600. Int J Mol Med. 2006. PMID: 16964410

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