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 em 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 em 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 em 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 em 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 em 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 em 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 em 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 em 2013

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 no Pediatr Rheumatol Online J (2015)

Color of Colon Content of Normal and Intrauterine Growth-Restricted Weaned Piglets is Associated with Specific Microbial Taxa and Physiological Parameters

Por Maria Wiese, Yan Hui, Dennis S. Nielsen, Andrew R. Williams, Julie C. Lynegaard, Nicolai R. Weber, Charlotte Amdi
Publicado em 2020-06-01

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 em 2013

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 em 2013

PReS-FINAL-2096: Herpes virus infections in patients with juvenile idiopathic arthritis (JIA) treated with etanercept

Por Nicolai, R, Cortis, E, Ravà, L, Bracaglia, C, Pardeo, M, Insalaco, A, Buonuomo, PS, De Benedetti, F, Tozzi, AE
Publicado em 2013

Modulation of methylation in the FMR1 promoter region after long term treatment with L-carnitine and acetyl-L-carnitine

Por Pascale, E, Battiloro, E, Reale, G, Pietrobono, R, Pomponi, M, Chiurazzi, P, Nicolai, R, Calvani, M, Neri, G, D'Ambrosio, E
Publicado em 2003

Genetic and antibody-mediated reprogramming of natural killer cell missing-self recognition in vivo

Por Sola, Caroline, André, Pascale, Lemmers, Céline, Fuseri, Nicolas, Bonnafous, Cécile, Bléry, Mathieu, Wagtmann, Nicolai R., Romagné, François, Vivier, Eric, Ugolini, Sophie
Publicado em 2009

PReS-FINAL-2142: Predictors of persistent remission following etanercept (ETN) withdrawal in patients with juvenile idiopathic arthritis (JIA)

Por Perfetti, F, Gesualdo, F, Messia, V, Insalaco, A, Bracaglia, C, Pardeo, M, Nicolai, R, Meli, L, De Benedetti, F, Magni Manzoni, S
Publicado em 2013

Cutting Edge: Identification of Neutrophil PGLYRP1 as a Ligand for TREM-1

Por Read, Christine B., Kuijper, Joseph L., Hjorth, Siv A., Heipel, Mark D., Tang, Xiaoting, Fleetwood, Andrew J., Dantzler, Jeffrey L., Grell, Susanne N., Kastrup, Jesper, Wang, Camilla, Brandt, Cameron S., Hansen, Anker J., Wagtmann, Nicolai R., Xu, Wenfeng, Stennicke, Vibeke W.
Publicado no J Immunol (2015)