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An international consensus approach to the management of atypical hemolytic uremic syndrome in children.
Loirat C, Fakhouri F, Ariceta G, Besbas N, Bitzan M, Bjerre A, Coppo R, Emma F, Johnson S, Karpman D, Landau D, Langman CB, Lapeyraque AL, Licht C, Nester C, Pecoraro C, Riedl M, van de Kar NC, Van de Walle J, Vivarelli M, Frémeaux-Bacchi V; HUS International. Loirat C, et al. Among authors: emma f. Pediatr Nephrol. 2016 Jan;31(1):15-39. doi: 10.1007/s00467-015-3076-8. Epub 2015 Apr 11. Pediatr Nephrol. 2016. PMID: 25859752 Review.
Type IV Bartter syndrome: report of two new cases.
Zaffanello M, Taranta A, Palma A, Bettinelli A, Marseglia GL, Emma F. Zaffanello M, et al. Among authors: emma f. Pediatr Nephrol. 2006 Jun;21(6):766-70. doi: 10.1007/s00467-006-0090-x. Epub 2006 Apr 1. Pediatr Nephrol. 2006. PMID: 16583241 Free article.
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: emma f. Nephrol Dial Transplant. 2009 Jun;24(6):1851-7. doi: 10.1093/ndt/gfn720. Epub 2008 Dec 25. Nephrol Dial Transplant. 2009. PMID: 19110485
279 results