238 results on '"Caorsi R"'
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2. Characterization of tonsil infiltration and gene expression profile of innate sensors in PFAPA patients
3. Canakinumab in the routinary clinical practice in cryopyrin-associated periodic syndromes (CAPS): one year of follow-up
4. Do parent's global rating of well-being and disease activity of children with juvenile idiopathic arthritis yield different information?
5. Prospective validation of the diagnostic score for molecular analysis of hereditary autoinflammatory syndromes in Italian children with periodic fever
6. Breaking down the fences among registries on autoinflammatory diseases: the E-Merge project
7. POS0784 CHRONIC RECURRENT MULTIFOCAL OSTEOMYELITIS ASSOCIATED TO INFLAMMATORY BOWEL DISEASES: EVIDENCES FOR A POSSIBLE ASSOCIATION. A SINGLE CENTER STUDY
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. POS0277 SYSTEMIC JUVENILE IDIOPATHIC ARTHRITIS ASSOCIATED LUNG DISEASE IN EUROPE
11. AB1437 NAILFOLD CAPILLAROSCOPY IN DEFICIENCY OF ADENOSINE DEAMINASE 2 (DADA2): A CASE-CONTROL STUDY
12. Interleukin-1 blockade for recurrent pericarditis: Insights from the real-world experience
13. Curation and expansion of the Human Phenotype Ontology for systemic autoinflammatory diseases improves phenotype-driven disease-matching.
14. Whole exome sequencing approach to childhood onset familial erythrodermic psoriasis unravels a novel mutation of CARD14 requiring unusual high doses of ustekinumab
15. Expanding the clinical and neuroimaging features of post-varicella arteriopathy of childhood
16. Defining Kawasaki disease and pediatric inflammatory multisystem syndrome-temporally associated to SARS-CoV-2 infection during SARS-CoV-2 epidemic in Italy: results from a national, multicenter survey
17. Curation and expansion of Human Phenotype Ontology for defined groups of inborn errors of immunity
18. POS1305 PEDIATRIC SAPHO SYNDROME: SINGLE ENTITY OR COMBINATION OF DIFFERENT DISEASES?
19. Defining Kawasaki disease and pediatric inflammatory multisystem syndrome-temporally associated to SARS-CoV-2 infection during SARS-CoV-2 epidemic in Italy: results from a national, multicenter survey
20. 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)
21. Widening the Neuroimaging Features of Adenosine Deaminase 2 Deficiency
22. Long-term clinical profile of children with the low-penetrance R92Q mutation of the TNFRSF1A gene
23. Clinical presentation and pathogenesis of cold-induced autoinflammatory disease in a family with recurrence of an NLRP12 mutation
24. OP0293 USE OF WHOLE-BODY MAGNETIC RESONANCE TO IDENTIFY POTENTIAL DIAGNOSTIC CLUES IN CHILDREN WITH FEVER OF UNKNOWN ORIGIN (FUO)
25. THU0501 EARLY DIAGNOSIS OF THE AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME (ALPS) IN PATIENTS WITH UNDEFINED AUTOINFLAMMATORY OR AUTOIMMUNE DISORDERS: THE PRACTICAL ROLE OF A FLOW CYTOMETRY PANEL
26. DESENSITIZATION TO ANAKINRA IN REFRACTORY RECURRENT PERICARDITIS
27. Successful treatment of co‐existent SAPHO syndrome and hidradenitis suppurativa with adalimumab and methotrexate
28. A web-based collection of genotype-phenotype associations in hereditary recurrent fevers from the Eurofever registry
29. NAILFOLD CAPILLAROSCOPY IN DEFICIENCY OF ADENOSINE DEAMINASE 2 (DADA2): A CASECONTROL STUDY.
30. A web-based collection of genotype-phenotype associations in hereditary recurrent fevers from the Eurofever registry
31. Type I interferonopathies in pediatric rheumatology
32. Inflammatory myopathy in a patient with collagen VI mutations
33. Use of Canakinumab in the Routinary Clinical Practice in Severe Cryopyrin-Associated Periodic Syndrome: One Year of Follow-up
34. The phenotypic variability of PAPA syndrome : Evidence from the Eurofever Registry
35. The phenotypic variability of PAPA syndrome: Evidence from the Eurofever Registry
36. SYSTEMIC JUVENILE IDIOPATHIC ARTHRITIS ASSOCIATED LUNG DISEASE IN EUROPE.
37. The Incidence of Multisystem Inflammatory syndrome in a Pediatric Emergency Department.
38. Rapid and sustained effect of anti-TNF treatment in patients with ADA2 deficiency
39. Distinct cerebrovascular features in patients with ADA2 deficiency
40. B cells characterization in ADA2 Deficiency patients
41. Identification of type I interferonopathies using blood interferon signature: the experience of a pediatric rheumatology center
42. Juvenile eosinophilic fasciitis: report of three cases with a review of the literature
43. Prevalence of CECR1 mutations in pediatric patients with polyarteritis nodosa, livedo reticularis and/or stroke
44. Enlarging the clinical spectrum of SAVI syndrome
45. Recruitment of abundant NK cells to the PFAPA tonsils support the crucial role of innate immunity in pathogenesis of PFAPA syndrome
46. Long-term efficacy of IL-1 blockers in PAPA patients
47. A Next Generation Sequencing approach to the mutational screening of patients affected with systemic autoinflammatory disorders: diagnosis improvement and interpretation of complex clinical phenotypes
48. The phenotypic variability of PAPA syndrome: evidence from the Eurofever Registry
49. FRI0526 Long-Term Efficacy of IL-1 Blockers in Papa Patients: Table 1
50. AB0644 B Cell Characterization in ADA2 Deficiency Patients
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