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24 results on '"Worth, Austen"'

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

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

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

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

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

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

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

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

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

11. One hundred percent survival after transplantation of 34 patients with Wiskott-Aldrich syndrome over 20 years

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

14. Non-posttransplant lymphoproliferative disorder malignancy after hematopoietic stem cell transplantation in patients with primary immunodeficiency: UK experience

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

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

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

18. Thymus transplantation for complete DiGeorge syndrome: European experience

19. A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis

20. Effect of stem cell source on long-term chimerism and event-free survival in children with primary immunodeficiency disorders after fludarabine and melphalan conditioning regimen

21. The extended phenotype of LPS-responsive beige-like anchor protein (LRBA) deficiency

22. Host natural killer immunity is a key indicator of permissiveness for donor cell engraftment in patients with severe combined immunodeficiency

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

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

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