960 results on '"Warnatz, Klaus"'
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2. Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency.
3. Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome.
4. Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency
5. An International Survey of Allogeneic Hematopoietic Cell Transplantation for X-Linked Agammaglobulinemia
6. Combined Immunodeficiency Caused by a Novel Nonsense Mutation in LCK
7. Evaluation of Laboratory and Sonographic Parameters for Detection of Portal Hypertension in Patients with Common Variable Immunodeficiency.
8. The GAIN Registry — a New Prospective Study for Patients with Multi-organ Autoimmunity and Autoinflammation
9. A Toolkit for Monitoring Immunoglobulin G Levels from Dried Blood Spots of Patients with Primary Immunodeficiencies
10. Age-associated B cells predict impaired humoral immunity after COVID-19 vaccination in patients receiving immune checkpoint blockade
11. Total escape of SARS-CoV-2 from dual monoclonal antibody therapy in an immunocompromised patient
12. International retrospective study of allogeneic hematopoietic cell transplantation for activated PI3K-delta syndrome.
13. Human memory B cells show plasticity and adopt multiple fates upon recall response to SARS-CoV-2
14. Grundlagen der Diagnostik primärer Immunstörungen („inborn errors of immunity“)
15. Abnormal biomarkers predict complex FAS or FADD defects missed by exome sequencing
16. Sequencing the B Cell Receptor Repertoires of Antibody-Deficient Individuals With and Without Infection Susceptibility
17. CVID-Associated B Cell Activating Factor Receptor Variants Change Receptor Oligomerization, Ligand Binding, and Signaling Responses
18. Interferon-Driven Immune Dysregulation in Common Variable Immunodeficiency–Associated Villous Atrophy and Norovirus Infection
19. Current Transition Practice for Primary Immunodeficiencies and Autoinflammatory Diseases in Europe: a RITA-ERN Survey
20. Telomere biology disorders may manifest as common variable immunodeficiency (CVID)
21. Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity
22. A distinct CD38+CD45RA+ population of CD4+, CD8+, and double-negative T cells is controlled by FAS.
23. Coronavirus disease 2019 in patients with inborn errors of immunity: An international study
24. The efficacy and safety of systemic corticosteroids as first line treatment for granulomatous lymphocytic interstitial lung disease
25. Publisher Correction: Human memory B cells show plasticity and adopt multiple fates upon recall response to SARS-CoV-2
26. Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients
27. Evaluation of Laboratory and Sonographic Parameters for Detection of Portal Hypertension in Patients with Common Variable Immunodeficiency
28. Interstitielle Lungenerkrankung bei CVID
29. Distinct CD8 T Cell Populations with Differential Exhaustion Profiles Associate with Secondary Complications in Common Variable Immunodeficiency
30. Early and Rapid Identification of COVID-19 Patients with Neutralizing Type I Interferon Auto-antibodies
31. The ABACHAI clinical trial protocol: Safety and efficacy of abatacept (s.c.) in patients with CTLA-4 insufficiency or LRBA deficiency: A non controlled phase 2 clinical trial
32. Mechanisms of CD8+ T-cell failure in chronic hepatitis E virus infection
33. Genomic characterization of lymphomas in patients with inborn errors of immunity
34. Case Series: Convalescent Plasma Therapy for Patients with COVID-19 and Primary Antibody Deficiency
35. Pembrolizumab for treatment of progressive multifocal leukoencephalopathy in primary immunodeficiency and/or hematologic malignancy: a case series of five patients
36. Single-cell Atlas of common variable immunodeficiency shows germinal center-associated epigenetic dysregulation in B-cell responses
37. Subcutaneous Gammanorm® by pump or rapid push infusion: Impact of the device on quality of life in adult patients with primary immunodeficiencies
38. Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations
39. Hypogammaglobulinemia and immune dysregulation—not just 2 sides of a coin
40. Immunoglobulin Class Switch Recombination Defects
41. IgA Deficiency With or Without IgG Subclass Deficiencies
42. IgG Subclass Deficiency and Specific Polysaccharide Antibody Deficiency (SPAD)
43. Good Syndrome
44. Common Variable Immunodeficiency (CVID)
45. CD20 Deficiency, Lessons Related to Therapeutic Biologicals and Primary Immunodeficiency
46. CD19 Deficiency Due to Genetic Defects in the CD19 and CD81 Genes
47. WHIM Syndrome
48. TACI and CVID
49. Activated PI3-Kinase Delta Syndrome (APDS)/p110d-Activating Mutations Causing Senescent T Cells, Lymphadenopathy, and Immunodeficiency (PASLI)
50. Altered Spectrum of Lymphoid Neoplasms in a Single-Center Cohort of Common Variable Immunodeficiency with Immune Dysregulation
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