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Hyperglycaemia and β-cell antibodies: is it always pre-type 1 diabetes?
d'Annunzio G, Marchi M, Aloi C, Salina A, Lugani F, Lorini R. d'Annunzio G, et al. Among authors: lugani f. Diabetes Res Clin Pract. 2013 Apr;100(1):e20-2. doi: 10.1016/j.diabres.2013.01.003. Epub 2013 Jan 24. Diabetes Res Clin Pract. 2013. PMID: 23352578
Wolfram syndrome: new mutations, different phenotype.
Aloi C, Salina A, Pasquali L, Lugani F, Perri K, Russo C, Tallone R, Ghiggeri GM, Lorini R, d'Annunzio G. Aloi C, et al. Among authors: lugani f. PLoS One. 2012;7(1):e29150. doi: 10.1371/journal.pone.0029150. Epub 2012 Jan 4. PLoS One. 2012. PMID: 22238590 Free PMC article.
Glucokinase mutations in pediatric patients with impaired fasting glucose.
Aloi C, Salina A, Minuto N, Tallone R, Lugani F, Mascagni A, Mazza O, Cassanello M, Maghnie M, d'Annunzio G. Aloi C, et al. Among authors: lugani f. Acta Diabetol. 2017 Oct;54(10):913-923. doi: 10.1007/s00592-017-1021-y. Epub 2017 Jul 19. Acta Diabetol. 2017. PMID: 28726111
Renal involvement and Strømme syndrome.
Caridi G, Lugani F, Lerone M, Divizia MT, Ghiggeri GM, Verrina E. Caridi G, et al. Among authors: lugani f. Clin Kidney J. 2020 Jan 25;14(1):439-441. doi: 10.1093/ckj/sfz189. eCollection 2021 Jan. Clin Kidney J. 2020. PMID: 33564452 Free PMC article.
Mutations in DSTYK and dominant urinary tract malformations.
Sanna-Cherchi S, Sampogna RV, Papeta N, Burgess KE, Nees SN, Perry BJ, Choi M, Bodria M, Liu Y, Weng PL, Lozanovski VJ, Verbitsky M, Lugani F, Sterken R, Paragas N, Caridi G, Carrea A, Dagnino M, Materna-Kiryluk A, Santamaria G, Murtas C, Ristoska-Bojkovska N, Izzi C, Kacak N, Bianco B, Giberti S, Gigante M, Piaggio G, Gesualdo L, Vukic DK, Vukojevic K, Saraga-Babic M, Saraga M, Gucev Z, Allegri L, Latos-Bielenska A, Casu D, State M, Scolari F, Ravazzolo R, Kiryluk K, Al-Awqati Q, D'Agati VD, Drummond IA, Tasic V, Lifton RP, Ghiggeri GM, Gharavi AG. Sanna-Cherchi S, et al. Among authors: lugani f. N Engl J Med. 2013 Aug 15;369(7):621-9. doi: 10.1056/NEJMoa1214479. Epub 2013 Jul 17. N Engl J Med. 2013. PMID: 23862974 Free PMC article.
Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy.
Caridi G, Lugani F, Dagnino M, Gigante M, Iolascon A, Falco M, Graziano C, Benetti E, Dugo M, Del Prete D, Granata A, Borracelli D, Moggia E, Quaglia M, Rinaldi R, Gesualdo L, Ghiggeri GM. Caridi G, et al. Among authors: lugani f. Nephrol Dial Transplant. 2014 Sep;29 Suppl 4:iv80-6. doi: 10.1093/ndt/gfu071. Nephrol Dial Transplant. 2014. PMID: 25165188
89 results