579 results on '"Gattorno, M"'
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2. Breaking down the fences among registries on autoinflammatory diseases: the E-Merge project
3. Whole exome sequencing approach to childhood onset familial erythrodermic psoriasis unravels a novel mutation of CARD14 requiring unusual high doses of ustekinumab
4. Corrigendum to The impact of the Eurofever criteria and the new InFevers MEFV classification in real life: Results from a large international FMF cohort (Seminars in Arthritis and Rheumatism (2022) 52, (S0049017222000087), (10.1016/j.semarthrit.2022.151957)): <[ Seminars in Arthritis and Rheumatism Volume 52, 151957]>
5. Phenotypic and genotypic characteristics of cryopyrin-associated periodic syndrome: a series of 136 patients from the Eurofever Registry
6. Pyrin and PSTPIP1, mutated in FMF, PAPA-, and PAMI syndrome, are involved in the hypersecretion of alarmins MRP8/14: 5.31
7. Defining colchicine resistance/intolerance in patients with familial Mediterranean fever: a modified-Delphi consensus approach
8. Contact tracing, use of surgical masks, hand hygiene and social distancing represent a bundle of effective measures to control SARS-CoV-2 spreading among healthcare workers in a paediatric hospital
9. Effect of anakinra on mortality in patients with COVID-19: a systematic review and patient-level meta-analysis
10. Erratum: Haploidentical α/β T-cell and B-cell depleted stem cell transplantation in severe mevalonate kinase deficiency (Rheumatology (2021) DOI: 10.1093/rheumatology/keaa912)
11. Two siblings presenting with novel ADA2 variants, lymphoproliferation, persistence of large granular lymphocytes, and T-cell perturbations
12. The phenotype of TNF receptor-associated autoinflammatory syndrome (TRAPS) at presentation: a series of 158 cases from the Eurofever/EUROTRAPS international registry
13. Erratum: Next generation sequencing panel in undifferentiated autoinflammatory diseases identifies patients with colchicine-responder recurrent fevers (Rheumatology (2020) 59 (344-60) DOI: 10.1093/rheumatology/kez270)
14. Significance of I313V mutation of NLPR3 gene in two pediatric patients
15. National CAPS (Cryopyrin-Associated Periodic Syndrome) Registry
16. Characterization of tonsil infiltration and gene expression profile of innate sensors in PFAPA patients
17. A novel mutatioin in the PSTPIP1 gene is associated with an autoinflammatory disease distinct from classical PAPA syndrome
18. International cohort study for pediatric Behçet’s Disease: update 2011
19. Dosing patterns of canakinumab in patients with Cryopyrin-Associated Periodic Syndromes (CAPS): A comparative analysis of a study in Western versus Japanese patients
20. The Eurofever Registry for autoinflammatory diseases: results of the first 15 months of enrolment
21. Canakinumab in the routinary clinical practice in cryopyrin-associated periodic syndromes (CAPS): one year of follow-up
22. Unexplained recurrent fever: when is autoinflammation the explanation?
23. Different pattern of synthesis and secretion of IL-1beta in patients with CIAS-1 and TNFRSF1A mutations responding to IL-1 blockade
24. Characterization of B cells in synovial fluid and tissue from patients with JIA
25. IL-1 beta receptor antagonist efficacy in the treatment of idiopathic recurrent pericarditis
26. International PFAPA syndrome registry: cohort of 214 patients
27. Efficacy of tonsillectomy in a family with a PFAPA-like phenotype
28. 12.3 Long-term follow up of patients with CINCA syndrome: efficacy and tolerability of Anakinra treatment
29. Prospective validation of the diagnostic score for molecular analysis of hereditary autoinflammatory syndromes in Italian children with periodic fever
30. Prevalence of monogenic autoinflammatory diseases among Pediatric Rheumatology centers: the Eurofever PReS/PRINTO survey
31. How not to miss autoinflammatory diseases masquerading as urticaria
32. Guidelines for the genetic diagnosis of hereditary recurrent fevers
33. 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
34. Long-term clinical profile of children with the low-penetrance R92Q mutation of the TNFRSF1A gene
35. Clinical presentation and pathogenesis of cold-induced autoinflammatory disease in a family with recurrence of an NLRP12 mutation
36. Efficacy and Safety of Canakinumab in a Large Cohort of Cryopyrin-Associated Periodic Syndrome (CAPS) Patients across All Severity Phenotypes: 874
37. Erratum: The multifaceted presentation of chronic recurrent multifocal osteomyelitis: a series of 486 cases from the Eurofever international registry (Rheumatology (Oxford, England) (2018))
38. A Diagnostic Score for Molecular Analysis of Hereditary Autoinflammatory Syndromes With Periodic Fever in Children
39. Persistent efficacy of anakinra in patients with tumor necrosis factor receptor–associated periodic syndrome
40. The longitudinal Eurofever project: an update on enrollment
41. DESENSITIZATION TO ANAKINRA IN REFRACTORY RECURRENT PERICARDITIS
42. Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies. Front Immunol. 2019 Apr 11;10:316. doi: 10.3389/fimmu.2019.00316. eCollection 2019. Erratum in: Front Immunol. 2019 May 31;10:1184
43. Corrigendum : Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies (Frontiers in Immunology (2019) 10 (316) DOI: 10.3389/fimmu.2019.00316)
44. Distinct expression pattern of IFN-α and TNF-α in juvenile idiopathic arthritis synovial tissue
45. Clinical and genetic characterization of Italian patients affected by CINCA syndrome
46. Lymphoid neogenesis in juvenile idiopathic arthritis correlates with ANA positivity and plasma cells infiltration
47. A polymorphic variant inside the osteopontin gene shows association with disease course in oligoarticular juvenile idiopathic arthritis
48. Synovial expression of osteopontin correlates with angiogenesis in juvenile idiopathic arthritis
49. Serum and synovial fluid concentration of vascular endothelial growth factor in juvenile idiopathic arthritides
50. Non-steroidal anti-inflammatory drugs in the treatment of hyper-IgD syndrome
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