Cargando…

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

Detalles Bibliográficos
Autores principales:	Pardeo, M, Insalaco, A, Bracaglia, C, Nicolai, R, Tozzi, AE, Prencipe, G, De Benedetti, F
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2013
Materias:	Meeting Abstract
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3952957/ http://dx.doi.org/10.1186/1546-0096-11-S1-A53

Ejemplares similares

PW01-039 – Long-term efficacy of anakinra in SoJIA patients
por: Naselli, A, et al.
Publicado: (2013)

P03-012 - A P268S NOD2 mutation in one Blau patient
por: Pardeo, M, et al.
Publicado: (2013)

PReS-FINAL-2096: Herpes virus infections in patients with juvenile idiopathic arthritis (JIA) treated with etanercept
por: Nicolai, R, et al.
Publicado: (2013)

P02-016 - A novel PSMB8 mutation causing candle syndrome
por: Messia, V, et al.
Publicado: (2013)

P02-031 - Phenotype of V198M and Q703K NLRP3 variants
por: Messia, V, et al.
Publicado: (2013)

P02-032 - CAPS: a novel mutation and an unusual phenotype
por: Insalaco, A, et al.
Publicado: (2013)

Cronic non-bacterial osteomyelitis (CNO) in a cohort of pediatric patients: clinical, biological and radiological response to treatment with Anakinra
por: Pardeo, M, et al.
Publicado: (2015)

P01-031 – Anakinra for colchicine resistant FMF
por: Ben-Zvi, I, et al.
Publicado: (2013)

P01-049 – Assessment of vascular function in systemic JIA
por: Sozeri, B, et al.
Publicado: (2013)

P01-048 – Systemic onset JIA with coronary artery dilation
por: Ayaz, N Aktay, et al.
Publicado: (2013)

PReS-FINAL-2142: Predictors of persistent remission following etanercept (ETN) withdrawal in patients with juvenile idiopathic arthritis (JIA)
por: Perfetti, F, et al.
Publicado: (2013)

PReS-FINAL-2199: A novel mutation in the CIAS1/NLRP3 gene associated with an unusual phenotype of CAPS
por: Insalaco, A, et al.
Publicado: (2013)

PW03-018 – Efficacy of Anakinra in recurrent pericarditis
por: Finetti, M, et al.
Publicado: (2013)

PW01-040 – Definition of polymorphism C3435T MDR1 gene in JIA
por: Rokhlina, F, et al.
Publicado: (2013)

PReS-FINAL-2201: A P268S NOD mutation in one Blau patient
por: Pardeo, M, et al.
Publicado: (2013)

Low levels of the nerve growth factor receptor TrkA in JIA: a possible defect in a novel anti-inflammatory mechanism
por: Minnone, G, et al.
Publicado: (2011)

Low levels of the nerve growth factor receptor TrkA in JIA: a possible defect in a novel anti-inflammatory mechanism
por: Minnone, G, et al.
Publicado: (2011)

PReS-FINAL-2202: A novel PSMB8 mutation associated with CANDLE syndrome
por: Insalaco, A, et al.
Publicado: (2013)

PReS-FINAL-2200: Phenotype of V198M and Q703K NLRP3 variants
por: Messia, V, et al.
Publicado: (2013)

Involvement of the IFN-gamma pathway in a patient with candle syndrome carrying a novel variant of PSMB8 gene
por: Insalaco, Antonella, et al.
Publicado: (2014)

P03-019 - Anakinra for sweet syndrome treatment
por: Passaro, G, et al.
Publicado: (2013)

Infliximab to treat chronic uveitis in juvenile idiopathic arthritis (JIA)
por: Bracaglia, C, et al.
Publicado: (2008)

P02-011 - TRAPS syndrome debuted as systemic JIA
por: Sleptsova, T, et al.
Publicado: (2013)

PReS-FINAL-2359: Renal involvement in hypocomplementemic urticarial vasculitis syndrome (huvs): report of 3 paediatric cases
por: Bracaglia, C, et al.
Publicado: (2013)

Single center experience in Next Generation Sequencing for genetic diagnosis of Autoinflammatory Disorders (AIDs)
por: Lepri, FR, et al.
Publicado: (2015)

PW02-003 - Efficacy of anakinra in etanercept-resistant TRAPS
por: Ombrello, AK, et al.
Publicado: (2013)

PW02-011 - Favorable response to anakinra in aisle patients
por: Ozdogan, H, et al.
Publicado: (2013)

An unusual presentation of purine nucleoside phosphorylase deficiency mimicking systemic juvenile idiopathic arthritis complicated by macrophage activation syndrome
por: Arduini, Alessia, et al.
Publicado: (2019)

PW02-039 - Long-term anakinra treatment in CAPS: a metaanalys
por: Leinonen, M, et al.
Publicado: (2013)

PW01-026 – Validation of pediatric diagnostic criteria in FMF
por: Demirkaya, E, et al.
Publicado: (2013)

Clinical presentation and cytokine production abnormalities in a cohort of patients carrying NLRP12 gene variants
por: Insalaco, Antonella, et al.
Publicado: (2014)

Anakinra in systemic juvenile idiopathic arthritis (soJIA) non responsive to antiTNF
por: Pontikaki, I, et al.
Publicado: (2008)

An Economic Comparison of Treatment Strategies with Anakinra in Systemic Juvenile Idiopathic Arthritis (sJIA)
por: Bullement, Ash, et al.
Publicado: (2021)

P01-013 – Cochlear involvement in FMF
por: Ayaz, N Aktay, et al.
Publicado: (2013)

P01-004 – MEFV genes and FMF
por: Salehzadeh, F, et al.
Publicado: (2013)

P01-003 – Bleeding disorder in FMF
por: Karadag, O, et al.
Publicado: (2013)

P01-011 – Colchicine compliance and amyloidosis
por: Ozdogan, H, et al.
Publicado: (2013)

P01-005 – Idiopathic uveitis and FMF
por: Salehzadeh, F, et al.
Publicado: (2013)

P01-029 – Microscopic hematuria in FMF
por: Grabowitz, L, et al.
Publicado: (2013)

P01-014 – Subclinical atherosclerosis in FMF
por: Ugurlu, S, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_00q32ojij8k32c56e7b61oo5v5