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2. New Dominant-Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130-Dependent Hyper-IgE Syndrome

5. Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection

7. JAK Inhibition in Aicardi-Goutières Syndrome: a Monocentric Multidisciplinary Real-World Approach Study

8. FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice

10. Preexisting autoantibodies to type I IFNs underlie critical COVID-19 pneumonia in patients with APS-1

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

12. Pregnancy in primary immunodeficiency diseases: The PREPI study

13. Correction to: New Dominant‑Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130‑Dependent Hyper‑IgE Syndrome

14. Monoclonal antibody-mediated neutralization of SARS-CoV-2 in an IRF9-deficient child

15. Inherited human RelB deficiency impairs innate and adaptive immunity to infection.

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

17. Differential Expression of Interferon-Alpha Protein Provides Clues to Tissue Specificity Across Type I Interferonopathies

18. Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency

20. Letermovir for CMV Prophylaxis in Very High-Risk Pediatric Hematopoietic Stem Cell Transplantation Recipients for Inborn Errors of Immunity

21. Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1

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

23. Déchiffrer les cahiers de doléances: Source, contextes et propositions d'économie politique (département de la Somme, 2018-2019).

25. Diffuse Endocapillary Glomerulonephritis in a Child With IL-17RA Deficiency Emphasizes the Pivotal Role of the Complement Cascade and Anaphylatoxins

27. Late-onset enteric virus infection associated with hepatitis (EVAH) in transplanted SCID patients

29. Human IL-23 is essential for IFN-γ–dependent immunity to mycobacteria

30. Human IRF1 governs macrophagic IFN-γ immunity to mycobacteria

31. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

33. A New Patient with p40phox Deficiency and Chronic Immune Thrombocytopenia.

34. Inherited CARD9 deficiency in otherwise healthy children and adults with Candida species–induced meningoencephalitis, colitis, or both

35. Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency

36. Inherited TNFSF9 deficiency causes broad Epstein–Barr virus infection with EBV+ smooth muscle tumors

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

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

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

41. Inherited human c-Rel deficiency disrupts myeloid and lymphoid immunity to multiple infectious agents

42. Impaired respiratory burst contributes to infections in PKCδ-deficient patients

43. Donor-targeted serotherapy as a rescue therapy for steroid-resistant acute GVHD after HLA-mismatched kidney transplantation

44. Herpes simplex encephalitis in a patient with a distinctive form of inherited IFNAR1 deficiency

47. Chronic mucocutaneous candidiasis and connective tissue disorder in humans with impaired JNK1-dependent responses to IL-17A/F and TGF-β

48. Bases génétiques de la candidose cutanéomuqueuse chronique chez l’homme

49. Genetic basis of chronic mucocutaneous candidiasis disease in humans

50. Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children

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