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266 results

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Increased NO production in lysinuric protein intolerance.
Mannucci L, Emma F, Markert M, Bachmann C, Boulat O, Carrozzo R, Rizzoni G, Dionisi-Vici C. Mannucci L, et al. Among authors: emma f. J Inherit Metab Dis. 2005;28(2):123-9. doi: 10.1007/s10545-005-5954-x. J Inherit Metab Dis. 2005. PMID: 15877200
"Bartter-like" phenotype in Kearns-Sayre syndrome.
Emma F, Pizzini C, Tessa A, Di Giandomenico S, Onetti-Muda A, Santorelli FM, Bertini E, Rizzoni G. Emma F, et al. Pediatr Nephrol. 2006 Mar;21(3):355-60. doi: 10.1007/s00467-005-2092-5. Epub 2005 Dec 29. Pediatr Nephrol. 2006. PMID: 16382326
Identification and subcellular localization of a new cystinosin isoform.
Taranta A, Petrini S, Palma A, Mannucci L, Wilmer MJ, De Luca V, Diomedi-Camassei F, Corallini S, Bellomo F, van den Heuvel LP, Levtchenko EN, Emma F. Taranta A, et al. Among authors: emma f. Am J Physiol Renal Physiol. 2008 May;294(5):F1101-8. doi: 10.1152/ajprenal.00413.2007. Epub 2008 Mar 12. Am J Physiol Renal Physiol. 2008. PMID: 18337546 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
[Multidisciplinary approach].
Bartuli A, Bertini E, Callea F, Cappa M, Caviglia S, D'argenio P, De Benedetti F, Digilio MC, Dionisi Vici C, El Hachem M, Emma F, Nobili V, Pagnotta G, Vignati E. Bartuli A, et al. Among authors: emma f. Minerva Pediatr. 2009 Dec;61(6):689-91. Minerva Pediatr. 2009. PMID: 19935526 Italian. No abstract available.
266 results