Infliximab to treat chronic uveitis in juvenile idiopathic arthritis (JIA)

por Bracaglia, C, Buonuomo, PS, Caminiti, S, Insalaco, A, Campana, A, Cortis, E
Publicado 2008

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

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

High membrane expression of CD163 by bone marrow cells is not a specific marker of macrophage activation syndrome (MAS)

por Bracaglia, C, Devito, R, Insalaco, A, Buonuomo, PS, Campana, A, Cortis, E, Ugazio, AG
Publicado 2008

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-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

Chronic recurrent multifocal osteomyelitis: 17 case reports and literature review

por Insalaco, A, Bozzola, E, Campana, A, Pagnotta, G, Toniolo, RM, Ciofetta, GC, Barbuti, D, Cortis, E
Publicado 2008

Identification of three ADA2 deficiency families with novel CECR1 mutations

por Sarrabay, G, Insalaco, A, Uettwiller, F, Tieulié, N, Quartier-dit-maire, P, Melki, J, Touitou, I
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

The phenotypic variability of PAPA syndrome: evidence from the Eurofever Registry

por Caorsi, R, Marotto, D, Insalaco, A, Marzano, A, Frenkel, J, Martini, A, De Benedetti, F, Gattorno, M
Publicado 2015

Inflammatory Cytokine response in a cohort of patients carrying novel NLRP12 variants

por Raganelli, L, Prencipe, G, Messia, V, Caiello, I, Lepri, FR, Pisaneschi, E, De Benedetti, F, Insalaco, A
Publicado 2015