PReS13-SPK-1590: Relevance of cytokine in pediatric inflammatory disease

por De Benedetti, F
Publicado 2013

PReS-FINAL-2183: IL-6 amplifies toll like receptor mediated cytokine and chemokine production: implications for the pathogenesis of rheumatic inflammatory diseases

por Caiello, I, Minnone, G, Holzinger, D, Vogl, T, De Benedetti, F, Strippoli, R
Publicado 2013

Neutralization of Interferon-gamma is efficacious in a mouse model of HLH secondary to chronic inflammation

por Prencipe, G, Caiello, I, Bracaglia, C, de Min, C, De Benedetti, F
Publicado 2015

P03-012 - A P268S NOD2 mutation in one Blau patient

por Pardeo, M, Cortis, E, Bracaglia, C, Nicolai, R, De Benedetti, F, Insalaco, A
Publicado 2013

OR6-005 – Cystine crystals activate inflammasomes

por Prencipe, G, Caiello, I, Petrini, S, Laudiero, L Bracci, Emma, F, De Benedetti, F
Publicado 2013

P02-016 - A novel PSMB8 mutation causing candle syndrome

por Messia, V, Pardeo, M, Nicolai, R, Bracaglia, C, De Benedetti, F, Insalaco, A
Publicado 2013

P02-031 - Phenotype of V198M and Q703K NLRP3 variants

por Messia, V, Pardeo, M, Nicolai, R, Bracaglia, C, De Benedetti, F, Insalaco, A
Publicado 2013

PReS-FINAL-2201: A P268S NOD mutation in one Blau patient

por Pardeo, M, Cortis, E, Bracaglia, C, Nicolai, R, De Benedetti, F, Insalaco, A
Publicado 2013

PReS-FINAL-2202: A novel PSMB8 mutation associated with CANDLE syndrome

por Insalaco, A, Messia, V, Pardeo, M, Nicolai, R, Bracaglia, C, De Benedetti, F
Publicado 2013

PReS-FINAL-2200: Phenotype of V198M and Q703K NLRP3 variants

por Messia, V, Pardeo, M, Nicolai, R, Bracaglia, C, De Benedetti, F, Insalaco, A
Publicado 2013

PW02-009 - PAPA syndrome: results from the Euroefever registry

por Caorsi, R, Insalaco, A, Marotto, D, Frenkel, J, Martini, A, De Benedetti, F, Gattorno, M
Publicado 2013

P02-032 - CAPS: a novel mutation and an unusual phenotype

por Insalaco, A, Buonuomo, PS, Bracaglia, C, Pardeo, M, Ceccherini, I, Nicolai, R, De Benedetti, F
Publicado 2013

P01-050 – Anakinra in systemic JIA: single center experience

por Pardeo, M, Insalaco, A, Bracaglia, C, Nicolai, R, Tozzi, AE, Prencipe, G, De Benedetti, F
Publicado 2013

PReS-FINAL-2070: Efficacy of biologic treatments in juvenile idiopathic arthritis with a polyarticular course: an indirect comparison

por Sawyer, L, Diamantopoulos, A, Brunner, HI, De Benedetti, F, Ruperto, N, Dejonckheere, F, Keane, C
Publicado 2013

PReS-FINAL-2238: PAPA (pyogenic arthritis, pyoderma gangrenosum and acne) syndrome: results from the Eurofever registry

por Caorsi, R, Insalaco, A, Marotto, D, Frenkel, J, Martini, A, De benedetti, F, Gattorno, M
Publicado 2013

Single center experience in Next Generation Sequencing for genetic diagnosis of Autoinflammatory Disorders (AIDs)

por Lepri, FR, Pisaneschi, E, Minervino, D, Messia, V, Pardeo, M, de Benedetti, F, Insalaco, A
Publicado 2015

Cronic non-bacterial osteomyelitis (CNO) in a cohort of pediatric patients: clinical, biological and radiological response to treatment with Anakinra

por Pardeo, M, Marafon, D Pires, Messia, V, Nicolai, R, Bracaglia, C, de Benedetti, F, Insalaco, A
Publicado 2015

PReS-FINAL-2199: A novel mutation in the CIAS1/NLRP3 gene associated with an unusual phenotype of CAPS

por Insalaco, A, Prencipe, G, Buonuomo, PS, Ceccherini, I, Bracaglia, C, Pardeo, M, Nicolai, R, De Benedetti, F
Publicado 2013

PReS-FINAL-2359: Renal involvement in hypocomplementemic urticarial vasculitis syndrome (huvs): report of 3 paediatric cases

por Bracaglia, C, Aceti, A, Vivarelli, M, Insalaco, A, Pardeo, M, Nicolai, R, De Benedetti, F, Pasini, A
Publicado 2013

Interferon gamma (IFNg) drives disease in the TLR9-mediated cytokine storm syndrome in mice

por de Min, C, Buatois, V, Chatel, L, Cons, L, De Benedetti, F, Kosco-Vilbois, M, Ferlin, W
Publicado 2015