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Page 1
Glomerulocystic kidney disease in hypomelanosis of Ito.
Vergine G, Mencarelli F, Diomedi-Camassei F, Caridi G, El Hachem M, Ghiggeri GM, Emma F. Vergine G, et al. Pediatr Nephrol. 2008 Jul;23(7):1183-7. doi: 10.1007/s00467-008-0797-y. Epub 2008 Apr 5. Pediatr Nephrol. 2008. PMID: 18392644
Drowning in Children and Predictive Parameters: A 15-Year Multicenter Retrospective Analysis.
Peri F, De Nardi L, Canuto A, Gaiero A, Noli S, Ferretti M, Vergine G, Falcioni A, Copponi E, Tagliabue B, Massart F, Fabiani E, Stringhi C, Rubini M, Zamagni G, Amaddeo A, Genovese MR, Norbedo S. Peri F, et al. Among authors: vergine g. Pediatr Emerg Care. 2023 Jul 1;39(7):516-523. doi: 10.1097/PEC.0000000000002987. Epub 2023 Jun 18. Pediatr Emerg Care. 2023. PMID: 37335544
The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis.
Palazzo V, Provenzano A, Becherucci F, Sansavini G, Mazzinghi B, Orlandini V, Giunti L, Roperto RM, Pantaleo M, Artuso R, Andreucci E, Bargiacchi S, Traficante G, Stagi S, Murer L, Benetti E, Emma F, Giordano M, Rivieri F, Colussi G, Penco S, Manfredini E, Caruso MR, Garavelli L, Andrulli S, Vergine G, Miglietti N, Mancini E, Malaventura C, Percesepe A, Grosso E, Materassi M, Romagnani P, Giglio S. Palazzo V, et al. Among authors: vergine g. Kidney Int. 2017 May;91(5):1243-1255. doi: 10.1016/j.kint.2016.12.017. Epub 2017 Feb 21. Kidney Int. 2017. PMID: 28233610 Free article.
Management of the congenital solitary kidney: consensus recommendations of the Italian Society of Pediatric Nephrology.
La Scola C, Ammenti A, Bertulli C, Bodria M, Brugnara M, Camilla R, Capone V, Casadio L, Chimenz R, Conte ML, Conversano E, Corrado C, Guarino S, Luongo I, Marsciani M, Marzuillo P, Meneghesso D, Pennesi M, Pugliese F, Pusceddu S, Ravaioli E, Taroni F, Vergine G, Peruzzi L, Montini G. La Scola C, et al. Among authors: vergine g. Pediatr Nephrol. 2022 Sep;37(9):2185-2207. doi: 10.1007/s00467-022-05528-y. Epub 2022 Jun 17. Pediatr Nephrol. 2022. PMID: 35713730 Free PMC article. Review.
Novel mutations of the CLCN5 gene including a complex allele and A 5' UTR mutation in Dent disease 1.
Tosetto E, Ceol M, Mezzabotta F, Ammenti A, Peruzzi L, Caruso MR, Barbano G, Vezzoli G, Colussi G, Vergine G, Giordano M, Glorioso N, Degortes S, Soldati L, Sayer J, D'Angelo A, Anglani F. Tosetto E, et al. Among authors: vergine g. Clin Genet. 2009 Oct;76(4):413-6. doi: 10.1111/j.1399-0004.2009.01212.x. Epub 2009 Aug 10. Clin Genet. 2009. PMID: 19673950 No abstract available.
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