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

4. Autoinflammatory patients with Golgi-trapped CDC42 exhibit intracellular trafficking defects leading to STING hyperactivation and ER stress

5. 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. Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease

10. Long-term and real-world safety and efficacy of retroviral gene therapy for adenosine deaminase deficiency

11. A Novel Heterozygous Variant in AICDA Impairs Ig Class Switching and Somatic Hypermutation in Human B Cells and is Associated with Autosomal Dominant HIGM2 Syndrome

12. Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee.

14. An International Survey of Allogeneic Hematopoietic Cell Transplantation for X-Linked Agammaglobulinemia

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

17. The HyperPed-COVID international registry: Impact of age of onset, disease presentation and geographical distribution on the final outcome of MIS-C

18. Wiskott-Aldrich syndrome: a study of 577 patients defines the genotype as a biomarker for disease severity and survival

20. Human Autosomal Recessive DNA Polymerase Delta 3 Deficiency Presenting as Omenn Syndrome

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

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

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

24. PLCG2-associated immune dysregulation (PLAID) comprises broad and distinct clinical presentations related to functional classes of genetic variants

27. The Ever-Increasing Array of Novel Inborn Errors of Immunity: an Interim Update by the IUIS Committee

28. Heterozygous mutations in the C-terminal domain of COPA underlie a complex autoinflammatory syndrome

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

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

31. Disrupted Ca2+ homeostasis and immunodeficiency in patients with functional IP3 receptor subtype 3 defects

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

33. Dominant-negative heterozygous mutations in AIRE confer diverse autoimmune phenotypes

34. Hematopoietic Cell Transplantation in Patients With Primary Immune Regulatory Disorders (PIRD): A Primary Immune Deficiency Treatment Consortium (PIDTC) Survey.

35. The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity

37. Hematopoietic stem cell transplantation for adolescents and adults with inborn errors of immunity: an EBMT IEWP study

39. Human inherited complete STAT2 deficiency underlies inflammatory viral diseases

40. Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons

41. From Your Nose to Your Toes: A Review of Severe Acute Respiratory Syndrome Coronavirus 2 Pandemic‒Associated Pernio

43. 94 Dominant negative IKKα and immunodeficiency with immune dysregulation

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

46. Cytopenia in autosomal dominant polycystic kidney disease (ADPKD): merely an association or a disease-related feature with prognostic implications?

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

49. Hematologically important mutations: X-linked chronic granulomatous disease (fourth update)

50. Simple Measurement of IgA Predicts Immunity and Mortality in Ataxia-Telangiectasia

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