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1. OP0135 MULTI-OMIC STUDY IN PATIENTS WITH SITRAME SYNDROME

2. Mutations de UNC93B1 : une nouvelle cause de lupus érythémateux systémique et de lupus-engelures monogéniques

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

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

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

8. 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

14. 489 Whole-transcriptome sequencing-based concomitant detection of viral and human genetic determinants of cutaneous lesions

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

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

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

19. Phenotypes of 126 Moroccan HIES patients according to NIH Score.

20. Correction: Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect.

21. Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect.

22. Hyperimmunoglobulinemia E and hereditary immune deficiencies.

23. Cytomegalovirus infection drives adaptive epigenetic diversification of NK cells with altered signaling and effector function.

24. Spotlight on NKG2C and the human NK-cell response to CMV infection.

25. Phenotype and function of natural killer cells in systemic lupus erythematosus: excess interferon-γ production in patients with active disease.

26. Shaping of iNKT cell repertoire after unrelated cord blood transplantation.

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