942 results on '"Gattorno, M"'
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2. Breaking down the fences among registries on autoinflammatory diseases: the E-Merge project
3. POS0767 CLINICAL AND SEROLOGICAL FEATURES OF PAEDIATRIC SJOGREN’S DISEASE AND COMPARISON WITH ADULT PATIENTS: A MULTICENTRE ITALIAN STUDY
4. POS0784 CHRONIC RECURRENT MULTIFOCAL OSTEOMYELITIS ASSOCIATED TO INFLAMMATORY BOWEL DISEASES: EVIDENCES FOR A POSSIBLE ASSOCIATION. A SINGLE CENTER STUDY
5. POS0156 CD4+HLADR+ T CELLS WITH AUTOIMMUNE REACTIVITY THAT RESIST REGULATORY CONTROL AND PERPETUATE DISEASE INFLAMMATION IN JUVENILE IDIOPATHIC ARTHRITIS
6. Les mutations gain de fonction de TLR7 sont à l’origine d’une maladie systémique et neuro-inflammatoire
7. AB0845 INVESTIGATING PERIPHERAL MICROCIRCULATION IN JUVENILE SJÖGREN’S SYNDROME: A PILOT STUDY USING NAILFOLD VIDEOCAPILLAROSCOPY
8. POS0773 STRATIFICATION OF PEDIATRIC SAPHO SYNDROME BASED ON SKIN MANIFESTATIONS: RESULTS FROM AN ITALIAN MULTICENTRIC STUDY (SAPHOPED)
9. Unravelling the clinical heterogeneity of undefined recurrent fever over time in the European registries on Autoinflammation
10. Thrombotic manifestations in pediatric Behçet syndrome: a multicenter comparative study from the EUROFEVER registry
11. Recurrent migratory angioedema as cutaneous manifestation in a familiar case of TRAPS: dramatic response to Anakinra
12. AB0007 DYNAMIC INTERPLAY OF FUNCTIONALLY DISCORDANT CD4+HLA-DR+ SUBSETS WITH A COMMON PATHOLOGICAL ONTOGENIC ORIGIN IN HUMAN ARTHRITIS
13. POS0740 VALIDATION OF THE PEDIATRIC BEHÇET DISEASE CRITERIA (PEDBD): A REAL LIFE CONSENSUS-BASED APPROACH
14. OP0254 INSIGHTS FROM A NOVEL MONOGENIC AUTOIMMUNE DISEASE: OVERVIEW OF A MULTICENTRIC EUROPEAN COHORT OF 27 PATIENTS WITH COPA SYNDROME
15. AB1437 NAILFOLD CAPILLAROSCOPY IN DEFICIENCY OF ADENOSINE DEAMINASE 2 (DADA2): A CASE-CONTROL STUDY
16. Curation and expansion of the Human Phenotype Ontology for systemic autoinflammatory diseases improves phenotype-driven disease-matching.
17. 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]>
18. Whole exome sequencing approach to childhood onset familial erythrodermic psoriasis unravels a novel mutation of CARD14 requiring unusual high doses of ustekinumab
19. Interleukin-1 blockade for recurrent pericarditis: Insights from the real-world experience
20. Expanding the clinical and neuroimaging features of post-varicella arteriopathy of childhood
21. The Italian Registry for Primary Immunodeficiencies (Italian Primary Immunodeficiency Network; IPINet): Twenty Years of Experience (1999–2019)
22. Two siblings presenting with novel ADA2 variants, lymphoproliferation, persistence of large granular lymphocytes, and T-cell perturbations
23. Curation and expansion of Human Phenotype Ontology for defined groups of inborn errors of immunity
24. Erste Analysen zu einer durch Patienten mit autoinflammatorischen Erkrankungen organisierten internationalen Befragung - FMF&AID
25. The 2021 EULAR/American College of Rheumatology Points to Consider for Diagnosis, Management and Monitoring of the Interleukin-1 Mediated Autoinflammatory Diseases: Cryopyrin-Associated Periodic Syndromes, Tumour Necrosis Factor Receptor-Associated Periodic Syndrome, Mevalonate Kinase Deficiency, and Deficiency of the Interleukin-1 Receptor Antagonist
26. Long-term efficacy and safety of canakinumab in patients with mevalonate kinase deficiency: results from the randomised Phase 3 CLUSTER trial
27. Deficiency in coatomer complex I causes aberrant activation of STING signalling
28. The impact of the Eurofever criteria and the new Infevers MEFV classification in real life: results from a large international FMF cohort
29. POS1365 THE FMF&AID SURVEY - A PATIENT ORGANIZATION DRIVEN SURVEY FOR AUTOINFLAMMATORY DISEASES
30. POS1372 THE 2021 EULAR AND ACR POINTS TO CONSIDER FOR DIAGNOSIS, MANAGEMENT AND MONITORING OF THE IL 1 MEDIATED AUTOINFLAMMATORY DISEASES: CAPS, TRAPS, MKD, AND DIRA
31. POS1305 PEDIATRIC SAPHO SYNDROME: SINGLE ENTITY OR COMBINATION OF DIFFERENT DISEASES?
32. Phenotypic and genotypic characteristics of cryopyrin-associated periodic syndrome: a series of 136 patients from the Eurofever Registry
33. Pyrin and PSTPIP1, mutated in FMF, PAPA-, and PAMI syndrome, are involved in the hypersecretion of alarmins MRP8/14: 5.31
34. Defining colchicine resistance/intolerance in patients with familial Mediterranean fever: a modified-Delphi consensus approach
35. 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
36. INSAID Variant Classification and Eurofever Criteria Guide Optimal Treatment Strategy in Patients with TRAPS: Data from the Eurofever Registry
37. Effect of anakinra on mortality in patients with COVID-19: a systematic review and patient-level meta-analysis
38. 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)
39. INSAID Variant Classification and Eurofever Criteria Guide Optimal Treatment Strategy in Patients with TRAPS: Data from the Eurofever Registry
40. Effect of anakinra on mortality in patients with COVID-19: a systematic review and patient-level meta-analysis
41. Persistence of disease flares is associated to an inadequate colchicine dose in familial Mediterranean fever: a national multicentre longitudinal study
42. Analisi socio-economica di lungo periodo di un paziente con una malattia reumatologica rara (CINCA)
43. Two siblings presenting with novel ADA2 variants, lymphoproliferation, persistence of large granular lymphocytes, and T-cell perturbations
44. The phenotype of TNF receptor-associated autoinflammatory syndrome (TRAPS) at presentation: a series of 158 cases from the Eurofever/EUROTRAPS international registry
45. POS1330 SAFETY OF ANAKINRA IN PATIENTS WITH CRYOPYRIN ASSOCIATED PERIODIC SYNDROMES (CAPS) USING A GRADUATED PRE-FILLED SYRINGE
46. A Systematic Review for the Management of the Genetically Defined Il-1-Mediated Autoinflammatory Diseases, Caps, Traps, Mkd and Dira
47. 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)
48. Health-Related Quality of Life and Emotional Difficulties in Chronic Granulomatous Disease: Data on Adult and Pediatric Patients from Italian Network for Primary Immunodeficiency (IPINet)
49. Significance of I313V mutation of NLPR3 gene in two pediatric patients
50. National CAPS (Cryopyrin-Associated Periodic Syndrome) Registry
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