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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
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
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: murer l. 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
Genetic risk factors in typical haemolytic uraemic syndrome.
Taranta A, Gianviti A, Palma A, De Luca V, Mannucci L, Procaccino MA, Ghiggeri GM, Caridi G, Fruci D, Ferracuti S, Ferretti A, Pecoraro C, Gaido M, Penza R, Edefonti A, Murer L, Tozzi AE, Emma F. Taranta A, et al. Among authors: murer l. Nephrol Dial Transplant. 2009 Jun;24(6):1851-7. doi: 10.1093/ndt/gfn720. Epub 2008 Dec 25. Nephrol Dial Transplant. 2009. PMID: 19110485
158 results