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1. Séquençage de l’exome chez des patients avec un syndrome d’Evans à début adulte : une cohorte de 80 patients

2. Inborn errors of OAS-RNase L in SARS-CoV-2-related multisystem inflammatory syndrome in children

3. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

5. Auto-antibodies against type I IFNs in patients with life-threatening COVID-19

6. X-linked recessive TLR7 deficiency in similar to 1% of men under 60 years old with life-threatening COVID-19

7. Autoantibodies neutralizing type I IFNs are present in similar to 4\% of uninfected individuals over 70 years old and account for similar to 20\% of COVID-19 deaths

8. Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths

9. Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths

10. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

11. Les auteurs

12. Erratum: Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome (J. Exp. Med. (2020) 217:6 Doi:10.1084/jem.20191804)

13. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

14. Autoantibodies against type I IFNs in patients with life-threatening COVID-19

15. Autoantibodies against type I IFNs in patients with life-threatening COVID-19

16. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

17. Auto-antibodies against type I IFNs in patients with life-threatening COVID-19

18. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

19. Acrosyndrome précoce et sévère : penser au déficit en ADA2

20. Haploidentical Hematopoietic Stem Cell Transplantation with Post-Transplant Cyclophosphamide for Primary Immunodeficiencies and Inherited Disorders in Children

21. Avarietyofalu-mediated copy number variations can underlie il-12rβ1 deficiency

22. Infections pulmonaires à mycobactéries non tuberculeuses sans facteur favorisant

24. Diagnosis of primary antibody and complement deficiencies in young adults after a first invasive bacterial infection

28. Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy

29. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

30. Human genetic and immunological determinants of critical COVID-19 pneumonia

31. The risk of COVID-19 death is much greater and age-dependent with type I IFN autoantibodies

32. Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths

33. T cell defects in patients with ARPC1B germline mutations account for their combined immunodeficiency

34. The Monogenic Landscape of Human Infectious Diseases.

35. 2q33 Deletions Underlying Syndromic and Non-syndromic CTLA4 Deficiency.

36. Incontinentia pigmenti underlies thymic dysplasia, autoantibodies to type I IFNs, and viral diseases.

37. Autoinflammation in patients with leukocytic CBL loss of heterozygosity is caused by constitutive ERK-mediated monocyte activation.

38. A sensitive assay for measuring whole-blood responses to type I IFNs.

39. Interferon Gamma in Sickness Predisposing to Mycobacterial Infectious Diseases

40. SARS-CoV-2 brainstem encephalitis in human inherited DBR1 deficiency.

41. Tuberculosis in otherwise healthy adults with inherited TNF deficiency.

42. Human inherited CCR2 deficiency underlies progressive polycystic lung disease.

43. Individuals with JAK1 variants are affected by syndromic features encompassing autoimmunity, atopy, colitis, and dermatitis.

44. Correction: Individuals with JAK1 variants are affected by syndromic features encompassing autoimmunity, atopy, colitis, and dermatitis.

45. Helper T cell immunity in humans with inherited CD4 deficiency.

46. Study of the potential role of CASPASE-10 mutations in the development of autoimmune lymphoproliferative syndrome.

47. Neutralizing IFN-γ autoantibodies are rare and pathogenic in HLA-DRB1*15:02 or 16:02 individuals.

48. The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants.

49. Human autoantibodies neutralizing type I IFNs: From 1981 to 2023.

50. Recombinant IFN-γ1b Treatment in a Patient with Inherited IFN-γ Deficiency.

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