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1. A corpus of GA4GH phenopackets: Case-level phenotyping for genomic diagnostics and discovery.

3. Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome.

4. European Society for Immunodeficiencies guidelines for the management of patients with congenital athymia

5. Variants in IGLL1 cause a broad phenotype from agammaglobulinemia to transient hypogammaglobulinemia

6. A corpus of GA4GH phenopackets: Case-level phenotyping for genomic diagnostics and discovery

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

9. Impact of newborn screening for SCID on the management of congenital athymia

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

13. Interferon-Driven Immune Dysregulation in Common Variable Immunodeficiency–Associated Villous Atrophy and Norovirus Infection

15. Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome

18. Allergic manifestations of inborn errors of immunity and their impact on the diagnosis: A worldwide study

19. Early-onset pulmonary and cutaneous vasculitis driven by constitutively active SRC-family kinase HCK

23. Impact of newborn screening for SCID on the management of congenital athymia

24. Resolution of granulomatous lesions in a Nijmegen breakage syndrome patient with severe immunodeficiency after hematopoietic stem cell transplantation.

28. Impact of newborn screening for SCID on the management of congenital athymia

31. Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome

32. Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome

34. Expanded population of lowdensity neutrophils in juvenile idiopathic arthritis.

35. News in immunology

37. Inborn errors of OAS–RNase L in SARS-CoV-2–related multisystem inflammatory syndrome in children

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

39. Novorozenecký screening vrozených poruch imunity – SCID screening.

40. Postvaccination Immunogenicity of BNT162b2 SARS-CoV-2 Vaccine and Its Predictors in Pediatric Inflammatory Bowel Disease

41. Interferon-Driven Immune Dysregulation in Common Variable Immunodeficiency–Associated Villous Atrophy and Norovirus Infection

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

44. B cells, BAFF and interferons in MIS-C

46. TLR8 / TLR7 dysregulation due to a novel TLR8 mutation causes severe autoimmune hemolytic anemia and autoinflammation in identical twins

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

50. Novinky v imunologii.

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