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1. Insufficient type I IFN immunity underlies life-threatening COVID-19 pneumonia

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

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

5. Vaccine breakthrough hypoxemic COVID-19 pneumonia in patients with auto-Abs neutralizing type I IFNs

6. Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency.

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

8. Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia.

9. Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency

10. Neutralizing IFN-[gamma] autoantibodies are rare and pathogenic in HLA-DRB1*15:02 or 16:02 individuals

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

13. Autoantibodies Neutralizing Type I IFNs in the Bronchoalveolar Lavage of at Least 10% of Patients During Life-Threatening COVID-19 Pneumonia

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

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

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

19. Anti-GM-CSF Neutralizing Autoantibodies in Colombian Patients with Disseminated Cryptococcosis

21. Mendelian Susceptibility to Mycobacterial Disease: Retrospective Clinical and Genetic Study in Mexico

22. List Of Contributors

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

27. Recalcitrant Cutaneous Warts in a Family with Inherited ICOS Deficiency

29. Correction: The oldest unvaccinated Covid-19 survivors in South America

30. The oldest unvaccinated Covid-19 survivors in South America

32. Human inherited complete STAT2 deficiency underlies inflammatory viral diseases

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

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

37. Monogenic etiologies of persistent human papillomavirus infections: a comprehensive systematic review

38. Homozygous NLRP1 gain-of-function mutation in siblings with a syndromic form of recurrent respiratory papillomatosis

40. RINT1 deficiency disrupts lipid metabolism and underlies a complex hereditary spastic paraplegia

43. Autoantibodies neutralizing type I IFNs underlie West Nile virus encephalitis in ∼40% of patients

44. Atypical Cutaneous Viral Infections Reveal an Inborn Error of Immunity in 8 Patients

47. List of Contributors

49. Impairment of Mycobacterial Immunity in Human Interleukin-12 Receptor Deficiency

50. Whole transcriptome–based skin virome profiling in typical epidermodysplasia verruciformis reveals α-, β-, and γ-HPV infections

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