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1. Murine Models of Familial Cytokine Storm Syndromes

2. Cardiac assessment and inflammatory markers in children with paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV2 (PIMS-TS) treated with methylprednisolone versus intravenous immunoglobulins: 6-month follow-up outcomes of the randomised controlled Swissped RECOVERY trial

4. Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity

6. Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations

7. Thrombotic Microangiopathy Associated with Macrophage Activation Syndrome: A Multinational Study of 23 Patients

8. A degranulation assay using Vγ9Vδ2 T cells for the rapid diagnosis of familial hemophagocytic syndromes.

9. Targeted busulfan-based reduced-intensity conditioning and HLA-matched HSCT cure hemophagocytic lymphohistiocytosis

10. Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity

11. Sequence-Specific Features of Short Double-Strand, Blunt-End RNAs Have RIG-I- and Type 1 Interferon-Dependent or -Independent Anti-Viral Effects

12. Therapeutic options for CTLA-4 insufficiency

13. The hyperinflammatory spectrum: from defects in cytotoxicity to cytokine control.

15. Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)

16. 2016 Classification Criteria for Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis: A European League Against Rheumatism/American College of Rheumatology/Paediatric Rheumatology International Trials Organisation Collaborative Initiative

17. Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations

18. Case report: ETS1 gene deletion associated with a low number of recent thymic emigrants in three patients with Jacobsen syndrome.

19. Thrombotic Microangiopathy Associated with Macrophage Activation Syndrome: A Multinational Study of 23 Patients

20. Multisystem Inflammation and Susceptibility to Viral infections in Human ZNFX1 Deficiency

23. Immunological Assessment of Pediatric Multisystem Inflammatory Syndrome Related to Coronavirus Disease 2019

24. Obesity-Induced Increase in Cystatin C Alleviates Tissue Inflammation

25. Swiss newborn screening for severe T and B cell deficiency with a combined TREC/KREC assay – management recommendations

26. 1698-P: Obesity-Induced Increase in Cystatin C Alleviates Tissue Inflammation and Hepatic Insulin Resistance

27. Maturation of the Human B-Cell Receptor Repertoire with Age

28. Immunological Assessment of Pediatric Multisystem Inflammatory Syndrome Related to Coronavirus Disease 2019.

29. Additional file 1: of Persistent mammalian orthoreovirus, coxsackievirus and adenovirus co-infection in a child with a primary immunodeficiency detected by metagenomic sequencing: a case report

30. Maturation of the human B-cell receptor repertoire with age

31. Disease evolution and response to rapamycin in activated phosphoinositide 3-kinase δ syndrome : The European society for immunodeficiencies-activated phosphoinositide 3-kinase δ syndrome registry

32. Obesity-Induced Increase in Cystatin C Alleviates Tissue Inflammation.

33. Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry

35. Proceedings of the 23rd Paediatric Rheumatology European Society Congress: part two: Genoa, Italy. 28 September – 01 October 2016

36. Hematopoietic stem cell transplantation in 29 patients hemizygous for hypomorphic IKBKG/NEMO mutations.

37. Distinct severity of HLH in both human and murine mutants with complete loss of cytotoxic effector PRF1, RAB27A, and STX11.

38. Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry

39. Germline mutations in a G protein identify signaling cross-talk in T cells.

40. Variants in IGLL1 cause a broad phenotype from agammaglobulinemia to transient hypogammaglobulinemia.

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