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48 results on '"Jansen, Machiel H."'

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1. A multi-platform approach to identify a blood-based host protein signature for distinguishing between bacterial and viral infections in febrile children (PERFORM): a multi-cohort machine learning study

2. Transient anti-cytokine autoantibodies superimpose the hyperinflammatory response in Kawasaki disease and multisystem inflammatory syndrome in children: a comparative cohort study on correlates of disease

6. A multi-platform approach to identify a blood-based host protein signature for distinguishing between bacterial and viral infections in febrile children (PERFORM): a multi-cohort machine learning study

7. Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

8. Transient anti-cytokine autoantibodies superimpose the hyperinflammatory response in Kawasaki disease and multisystem inflammatory syndrome in children: a comparative cohort study on correlates of disease

9. Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia Syndrome

11. Transient anti-cytokine autoantibodies superimpose the hyperinflammatory response in Kawasaki disease and multisystem inflammatory syndrome in children: a comparative cohort study on correlates of disease

12. A multi-platform approach to identify a blood-based host protein signature for distinguishing between bacterial and viral infections in febrile children (PERFORM):a multi-cohort machine learning study

17. Immunodeficiency, autoimmunity, and increased risk of B cell malignancy in humans with TRAF3 mutations

21. A combined immunodeficiency with severe infections, inflammation, and allergy caused by ARPC1B deficiency

25. Loss of function NFKB1 variants are the most common monogenic cause of CVID in Europeans

27. A combined immunodeficiency with severe infections, inflammation, and allergy caused by ARPC1B deficiency

28. Activated neutrophils exert myeloid-derived suppressor cell activity damaging T cells beyond repair

29. Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

31. Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

32. High‐throughput compound screen reveals mTOR inhibitors as potential therapeutics to reduce (auto)antibody production by human plasma cells.

35. Phenotypic variation in Aicardi-Goutières syndrome explained by cell-specific IFN-stimulated gene response and cytokine release

36. Aicardi-Goutières syndrome harbours abundant systemic and brain-reactive autoantibodies

37. Phenotypic variation in Aicardi-Goutières syndrome explained by cell-specific IFN-stimulated gene response and cytokine release

38. ADAR1 Facilitates HIV-1 Replication in Primary CD4+ T Cells

39. Phenotypic Variation in Aicardi–Goutières Syndrome Explained by Cell-Specific IFN-Stimulated Gene Response and Cytokine Release

42. Aicardi–Goutières syndrome harbours abundant systemic and brain-reactive autoantibodies

45. ADAR1 Facilitates HIV-1 Replication in Primary CD4+ T Cells.

46. Identification of B Cell Defects Using Age-Defined Reference Ranges for In Vivo and In Vitro B Cell Differentiation.

47. Idiopathic CD4+T lymphopenia without autoimmunity or granulomatous disease in the slipstream of RAG mutations

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