Significance of I313V mutation of NLPR3 gene in two pediatric patients

by Omenetti, A, Antona, R, Gallizzi, R, Alessio, M, Finetti, M, Carta, S, Rubartelli, A, Martini, A, Gattorno, M
Published 2011

PReS-FINAL-2196: The clinical significance of the Q703K mutation of NLRP3 gene. A multicentric national study

by Naselli, A, Cantarini, L, Insalaco, A, Alessio, M, Tommasini, A, Gallizzi, R, Signa, S, Lucherini, OM, Caroli, F, Ceccherini, I, Martini, A, Gattorno, M
Published 2013

National CAPS (Cryopyrin-Associated Periodic Syndrome) Registry

by Bibalo, C, Paloni, G, Lepore, L, Gattorno, M, Finetti, M, Zulian, F, Martini, G, Alessio, M, Cattalin, M, Stabile, A, Rigante, D, Insalaco, A, Manna, R, Gallizzi, R, Obici, L, Cantarini, L, Martino, S, Cionsolini, R
Published 2011

PW02-022 - Recurrent fever syndromes: multiple gene mutations

by Bohm, M, Dolezalova, P, Lachmann, H, Modesto, C, Touitou, I, Woo, P, Finetti, M, Hentgen, V, Cantarini, L, De Benedetti, F, Gallizzi, R, Obici, L, Manna, R, Gallo, E, Ruperto, N, Gattorno, M
Published 2013

Differences in therapeutic approach to juvenile dermatomyositis between Europe and Latin America

by Trail, L, Ferrari, C, Cuttica, R, Katsicas, MM, Russo, R, Bandeira, M, Ferriani, V, Oliveira, S, Saad-Magalhaes, C, Silva, CA, Baca, V, Burgos-Vargas, R, Solis-Vallejo, E, Maillard, S, Pilkington, C, Barcellona, R, Beltramelli, M, Breda, L, Bruno, C, Cimaz, R, Cortis, E, Gallizzi, R, Garofalo, F, Meini, A, Podda, R, Stabile, A, Martini, A, Ravelli, A
Published 2008

PReS-FINAL-2141: Clinical features, therapeutic interventions and outcome of 362 patients with macrophage activation syndrome enrolled in a multinational survey

by Minoia, F, Davì, S, Horne, A, Consolaro, A, Rosina, S, Davidsone, Z, De Cunto, C, De Inocencio, J, Eisenstein, E, Espada, G, Fishbach, M, Frosch, M, Gallizzi, R, Gamir, ML, Griffin, T, Grom, A, Hennon, T, Horneff, G, Huasong, Z, Ruperto, N, Martini, A, Cron, RQ, Ravelli, A
Published 2013