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

3. International retrospective study of allogeneic hematopoietic cell transplantation for activated PI3K-delta syndrome.

4. Favipiravir induces HuNoV viral mutagenesis and infectivity loss with clinical improvement in immunocompromised patients

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

6. Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients

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

9. A National Survey of Hereditary Angioedema and Acquired C1 Inhibitor Deficiency in the United Kingdom

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

11. Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients

13. Incremental donor lymphocyte infusion to treat mixed chimerism after allogeneic stem cell transplantation in children with non-malignant diseases

14. Retrospective, Landmark Analysis of Long-term Adult Morbidity Following Allogeneic HSCT for Inborn Errors of Immunity in Infancy and Childhood

16. Phenotype, genotype, treatment, and survival outcomes in patients with X-linked inhibitor of apoptosis deficiency

17. Hematopoietic cell transplantation in severe combined immunodeficiency: The SCETIDE 2006-2014 European cohort

18. Outcomes of X-Linked Agammaglobulinaemia Patients.

22. Reduced-Intensity/Reduced-Toxicity Conditioning Approaches Are Tolerated in XIAP Deficiency but Patients Fare Poorly with Acute GVHD

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

24. Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study.

25. Interleukin-1 blockade in patients with Wiskott-Aldrich syndrome: a retrospective multinational case series

26. Hematopoietic Stem Cell Transplantation Resolves the Immune Deficit Associated with STAT3-Dominant-Negative Hyper-IgE Syndrome

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

28. Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations

29. Persistent Low-Level Variants in a Subset of Viral Genes Are Highly Predictive of Poor Outcome in Immunocompromised Patients With Cytomegalovirus Infection.

30. Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency

31. Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

32. New insights into risk factors for transplant-associated thrombotic microangiopathy in pediatric HSCT

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

34. Novel antivirals for severe enterovirus infection in immunocompromised hosts; a case series

37. Outcome of Non-hematological Autoimmunity After Hematopoietic Cell Transplantation in Children with Primary Immunodeficiency

40. Neuroinflammatory Disease as an Isolated Manifestation of Hemophagocytic Lymphohistiocytosis

42. New graft manipulation strategies improve the outcome of mismatched stem cell transplantation in children with primary immunodeficiencies

45. Translating metagenomics into clinical practice for complex paediatric neurological presentations

47. Corrigendum to “Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients” [Clinical Immunology 255 (2023) 109757]

48. Treatment dilemmas in asymptomatic children with primary hemophagocytic lymphohistiocytosis

49. Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

50. T-cell receptor αβ+ and CD19+ cell–depleted haploidentical and mismatched hematopoietic stem cell transplantation in primary immune deficiency

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