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Your search keyword '"Meyts, Isabelle"' showing total 36 results

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36 results on '"Meyts, Isabelle"'

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1. Coronavirus disease 2019 in patients with inborn errors of immunity: An international study

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

3. Inherited and acquired errors of type I interferon immunity govern susceptibility to COVID-19 and multisystem inflammatory syndrome in children

4. Homozygous DBF4 mutation as a cause for severe congenital neutropenia

6. Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations

7. Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia

8. Cutaneous barrier leakage and gut inflammation drive skin disease in Omenn syndrome

9. Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score

10. Activating mutations in PIK3CD disrupt the differentiation and function of human and murine CD4+ T cells

11. Hematopoietic stem cell transplantation for CD40 ligand deficiency: Results from an EBMT/ESID-IEWP-SCETIDE-PIDTC study

12. Combined liver and hematopoietic stem cell transplantation in patients with X-linked hyper-IgM syndrome

14. Activating PIK3CD mutations impair human cytotoxic lymphocyte differentiation and function and EBV immunity

15. Abnormal differentiation of B cells and megakaryocytes in patients with Roifman syndrome

16. A kindred with mutant IKAROS and autoimmunity

17. Treatment of severe forms of LPS-responsive beige-like anchor protein deficiency with allogeneic hematopoietic stem cell transplantation

18. Clinical characteristics of patients with low functional IL-6 production upon TLR/IL-1R stimulation

19. Disease-associated mutations identify a novel region in human STING necessary for the control of type I interferon signaling

20. A novel kindred with inherited STAT2 deficiency and severe viral illness

21. Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation

23. Successful hematopoietic stem cell transplantation for myelofibrosis in an adult with warts-hypogammaglobulinemia-immunodeficiency-myelokathexis syndrome

24. Exome and genome sequencing for inborn errors of immunity

25. A novel hypomorphic mutation in STIM1 results in a late-onset immunodeficiency

26. Multicenter experience in hematopoietic stem cell transplantation for serious complications of common variable immunodeficiency

27. Hematopoietic stem cell transplantation rescues the immunologic phenotype and prevents vasculopathy in patients with adenosine deaminase 2 deficiency

28. Gain-of-function mutations in signal transducer and activator of transcription 1 (STAT1): Chronic mucocutaneous candidiasis accompanied by enamel defects and delayed dental shedding

29. Clinical picture and treatment of 2212 patients with common variable immunodeficiency

32. Granulomatous inflammation in cartilage-hair hypoplasia: Risks and benefits of anti–TNF-α mAbs

35. Homozygous DBF4 mutation as a cause of severe congenital neutropenia.

36. Activating mutations in PIK3CD disrupt the differentiation and function of human and murine CD4 + T cells.

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