about
Weekly oral alendronate in mevalonate kinase deficiencyWorking the endless puzzle of hereditary autoinflammatory disorders.Biological treatments in Behçet's disease: beyond anti-TNF therapy.First report of circulating microRNAs in tumour necrosis factor receptor-associated periodic syndrome (TRAPS).The common NOD2/CARD15 variant P268S in patients with non-infectious uveitis: a cohort study.Putative Role of Serum Amyloid-A and Proinflammatory Cytokines as Biomarkers for Behcet's Disease.Biological treatments: new weapons in the management of monogenic autoinflammatory disordersMonogenic autoinflammatory syndromes: state of the art on genetic, clinical, and therapeutic issuesSpecific recycling receptors are targeted to the immune synapse by the intraflagellar transport systemRole of autoimmunity and autoinflammation in the pathogenesis of idiopathic recurrent pericarditis.Autoinflammatory diseases and cardiovascular manifestations.Clinical and biochemical landmarks in systemic autoinflammatory diseases.The diagnostic evaluation of patients with potential adult-onset autoinflammatory disorders: our experience and review of the literature.Tumour necrosis factor receptor-associated periodic syndrome (TRAPS): state of the art and future perspectives.Expanding spectrum of TNFRSF1A gene mutations among patients with idiopathic recurrent acute pericarditis.The expanding spectrum of low-penetrance TNFRSF1A gene variants in adults presenting with recurrent inflammatory attacks: clinical manifestations and long-term follow-up.Early-onset sarcoidosis caused by a rare CARD15/NOD2 de novo mutation and responsive to infliximab: a case report with long-term follow-up and review of the literature.Key facts and hot spots on tumor necrosis factor receptor-associated periodic syndrome.The labyrinth of autoinflammatory disorders: a snapshot on the activity of a third-level center in Italy.Untangling the web of systemic autoinflammatory diseases.The hereditary autoinflammatory disorders uncovered.Caveats and truths in genetic, clinical, autoimmune and autoinflammatory issues in Blau syndrome and early onset sarcoidosis.The diagnostic evaluation of patients with a suspected hereditary periodic fever syndrome: experience from a referral center in Italy.Negative regulation of chemokine receptor signaling and B-cell chemotaxis by p66Shc.Clinical Characteristics of Patients Carrying the Q703K Variant of the NLRP3 Gene: A 10-year Multicentric National Study.Caution Should be Used in the Recognition of Adult-Onset Autoinflammatory Disorders: Facts or Fiction?Differential impact of high and low penetrance TNFRSF1A gene mutations on conventional and regulatory CD4+ T cell functions in TNFR1-associated periodic syndrome.IL-6 blockade in the management of non-infectious uveitis.Clues to detect tumor necrosis factor receptor-associated periodic syndrome (TRAPS) among patients with idiopathic recurrent acute pericarditis: results of a multicentre study.Colchicine myopathy and neuromyopathy: two cases with different characteristics.Typical and severe tumor necrosis factor receptor-associated periodic syndrome in the absence of mutations in the TNFRSF1A gene: a case series.Systemic-onset juvenile idiopathic arthritis complicated by early onset amyloidosis in a patient carrying a mutation in the MEFV gene.T-cell receptor early signalling complex activation in response to interferon-alpha receptor stimulation.Possible chondroprotective effect of canakinumab: an in vitro study on human osteoarthritic chondrocytes.Cytokine Signatures in Mucocutaneous and Ocular Behçet's Disease.Negative regulation of immunoreceptor signaling by protein adapters: Shc proteins join the club.Impaired expression of p66Shc, a novel regulator of B-cell survival, in chronic lymphocytic leukemia.Involvement of X-box binding protein 1 and reactive oxygen species pathways in the pathogenesis of tumour necrosis factor receptor-associated periodic syndrome.Inhibition of interleukin-1 by canakinumab as a successful mono-drug strategy for the treatment of refractory Behçet's disease: a case series.Role of polymorphonucleates in the pathogenesis of systemic juvenile idiopathic arthritis and Still's disease: a proof of concept study.
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Orso Maria Lucherini
@ast
Orso Maria Lucherini
@en
Orso Maria Lucherini
@es
Orso Maria Lucherini
@nl
Orso Maria Lucherini
@sl
type
label
Orso Maria Lucherini
@ast
Orso Maria Lucherini
@en
Orso Maria Lucherini
@es
Orso Maria Lucherini
@nl
Orso Maria Lucherini
@sl
prefLabel
Orso Maria Lucherini
@ast
Orso Maria Lucherini
@en
Orso Maria Lucherini
@es
Orso Maria Lucherini
@nl
Orso Maria Lucherini
@sl
P106
P1153
21834494800
P21
P31
P496
0000-0002-3314-0814
P569
2000-01-01T00:00:00Z