514 results on '"Gattorno, M"'
Search Results
2. Breaking down the fences among registries on autoinflammatory diseases: the E-Merge project
3. Recurrent migratory angioedema as cutaneous manifestation in a familiar case of TRAPS: dramatic response to Anakinra
4. Whole exome sequencing approach to childhood onset familial erythrodermic psoriasis unravels a novel mutation of CARD14 requiring unusual high doses of ustekinumab
5. Les mutations gain de fonction de TLR7 sont à l’origine d’une maladie systémique et neuro-inflammatoire
6. Phenotypic and genotypic characteristics of cryopyrin-associated periodic syndrome: a series of 136 patients from the Eurofever Registry
7. Pyrin and PSTPIP1, mutated in FMF, PAPA-, and PAMI syndrome, are involved in the hypersecretion of alarmins MRP8/14: 5.31
8. Analisi socio-economica di lungo periodo di un paziente con una malattia reumatologica rara (CINCA)
9. Two siblings presenting with novel ADA2 variants, lymphoproliferation, persistence of large granular lymphocytes, and T-cell perturbations
10. The phenotype of TNF receptor-associated autoinflammatory syndrome (TRAPS) at presentation: a series of 158 cases from the Eurofever/EUROTRAPS international registry
11. Significance of I313V mutation of NLPR3 gene in two pediatric patients
12. National CAPS (Cryopyrin-Associated Periodic Syndrome) Registry
13. Characterization of tonsil infiltration and gene expression profile of innate sensors in PFAPA patients
14. A novel mutatioin in the PSTPIP1 gene is associated with an autoinflammatory disease distinct from classical PAPA syndrome
15. International cohort study for pediatric Behçet’s Disease: update 2011
16. Dosing patterns of canakinumab in patients with Cryopyrin-Associated Periodic Syndromes (CAPS): A comparative analysis of a study in Western versus Japanese patients
17. The Eurofever Registry for autoinflammatory diseases: results of the first 15 months of enrolment
18. Canakinumab in the routinary clinical practice in cryopyrin-associated periodic syndromes (CAPS): one year of follow-up
19. Unexplained recurrent fever: when is autoinflammation the explanation?
20. Different pattern of synthesis and secretion of IL-1beta in patients with CIAS-1 and TNFRSF1A mutations responding to IL-1 blockade
21. Characterization of B cells in synovial fluid and tissue from patients with JIA
22. IL-1 beta receptor antagonist efficacy in the treatment of idiopathic recurrent pericarditis
23. International PFAPA syndrome registry: cohort of 214 patients
24. Efficacy of tonsillectomy in a family with a PFAPA-like phenotype
25. 12.3 Long-term follow up of patients with CINCA syndrome: efficacy and tolerability of Anakinra treatment
26. Prospective validation of the diagnostic score for molecular analysis of hereditary autoinflammatory syndromes in Italian children with periodic fever
27. Prevalence of monogenic autoinflammatory diseases among Pediatric Rheumatology centers: the Eurofever PReS/PRINTO survey
28. How not to miss autoinflammatory diseases masquerading as urticaria
29. Guidelines for the genetic diagnosis of hereditary recurrent fevers
30. Two-year results from an open-label, multicentre, phase III study evaluating the safety and efficacy of canakinumab in patients with cryopyrin-associated periodic syndrome across different severity phenotypes
31. Long-term clinical profile of children with the low-penetrance R92Q mutation of the TNFRSF1A gene
32. Clinical presentation and pathogenesis of cold-induced autoinflammatory disease in a family with recurrence of an NLRP12 mutation
33. Efficacy and Safety of Canakinumab in a Large Cohort of Cryopyrin-Associated Periodic Syndrome (CAPS) Patients across All Severity Phenotypes: 874
34. A Diagnostic Score for Molecular Analysis of Hereditary Autoinflammatory Syndromes With Periodic Fever in Children
35. Persistent efficacy of anakinra in patients with tumor necrosis factor receptor–associated periodic syndrome
36. Distinct expression pattern of IFN-α and TNF-α in juvenile idiopathic arthritis synovial tissue
37. Clinical and genetic characterization of Italian patients affected by CINCA syndrome
38. Lymphoid neogenesis in juvenile idiopathic arthritis correlates with ANA positivity and plasma cells infiltration
39. A polymorphic variant inside the osteopontin gene shows association with disease course in oligoarticular juvenile idiopathic arthritis
40. Synovial expression of osteopontin correlates with angiogenesis in juvenile idiopathic arthritis
41. Serum and synovial fluid concentration of vascular endothelial growth factor in juvenile idiopathic arthritides
42. Non-steroidal anti-inflammatory drugs in the treatment of hyper-IgD syndrome
43. Brother and sister with different vasculitides
44. Interactions between Prolactin and the Proinflammatory Cytokine Network in Juvenile Chronic Arthritis
45. Serum interleukin 12 concentration in juvenile chronic arthritis
46. Synovial fluid T cell clones from oligoarticular juvenile arthritis patients display a prevalent Th1/Th0-type pattern of cytokine secretion irrespective of immunophenotype
47. Widening the Neuroimaging Features of Adenosine Deaminase 2 Deficiency.
48. Neonatal lupus and a seronegative mother
49. NAILFOLD CAPILLAROSCOPY IN DEFICIENCY OF ADENOSINE DEAMINASE 2 (DADA2): A CASECONTROL STUDY.
50. REAL LIFE DATA ON TAPERING AND DISCONTINUATION OF ANAKINRA TREATMENT IN RECURRENT PERICARDITIS: AN INTERNATIONAL REGISTRY.
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