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Identification of fifteen novel mutations in the SLC12A3 gene encoding the Na-Cl Co-transporter in Italian patients with Gitelman syndrome.
Syrén ML, Tedeschi S, Cesareo L, Bellantuono R, Colussi G, Procaccio M, Alì A, Domenici R, Malberti F, Sprocati M, Sacco M, Miglietti N, Edefonti A, Sereni F, Casari G, Coviello DA, Bettinelli A. Syrén ML, et al. Among authors: edefonti a. Hum Mutat. 2002 Jul;20(1):78. doi: 10.1002/humu.9045. Hum Mutat. 2002. PMID: 12112667
Electrocardiogram with prolonged QT interval in Gitelman disease.
Bettinelli A, Tosetto C, Colussi G, Tommasini G, Edefonti A, Bianchetti MG. Bettinelli A, et al. Among authors: edefonti a. Kidney Int. 2002 Aug;62(2):580-4. doi: 10.1046/j.1523-1755.2002.00467.x. Kidney Int. 2002. PMID: 12110021 Free article.
Risk factors for poor renal prognosis in children with hemolytic uremic syndrome.
Gianviti A, Tozzi AE, De Petris L, Caprioli A, Ravà L, Edefonti A, Ardissino G, Montini G, Zacchello G, Ferretti A, Pecoraro C, De Palo T, Caringella A, Gaido M, Coppo R, Perfumo F, Miglietti N, Ratsche I, Penza R, Capasso G, Maringhini S, Li Volti S, Setzu C, Pennesi M, Bettinelli A, Peratoner L, Pela I, Salvaggio E, Lama G, Maffei S, Rizzoni G. Gianviti A, et al. Among authors: edefonti a. Pediatr Nephrol. 2003 Dec;18(12):1229-35. doi: 10.1007/s00467-003-1262-6. Epub 2003 Oct 31. Pediatr Nephrol. 2003. PMID: 14593522
Reduced coronary flow reserve in young adults with renal transplant.
Viganò SM, Turiel M, Martina V, Meregalli E, Tomasoni L, De Blasio G, Delfino L, Edefonti A, Grillo P, Procaccio M, Cusi D, Ghio L. Viganò SM, et al. Among authors: edefonti a. Nephrol Dial Transplant. 2007 Aug;22(8):2328-33. doi: 10.1093/ndt/gfm110. Epub 2007 Apr 23. Nephrol Dial Transplant. 2007. PMID: 17452415
249 results