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

2. Part 5: Allogeneic HSCT in refractory SJIA with lung disease; recent cases from centers in North America & Europe

3. NBEAL2 deficiency in humans leads to low CTLA-4 expression in activated conventional T cells

4. On behalf of the SFGM‐TC: Real‐life use of third‐party virus‐specific T‐cell transfer in immunocompromised transplanted patients

5. Sustained remission after haploidentical bone marrow transplantation in a child with refractory systemic juvenile idiopathic arthritis

6. Early-onset autoimmunity associated with SOCS1 haploinsufficiency

7. Bayesian Modeling Immune Reconstitution Apply to CD34+ Selected Stem Cell Transplantation for Severe Combined Immunodeficiency

8. Physicochemical Stability Study of Oral Suspension Containing Ruxolitinib in Children with Steroid-Refractory Acute Graft-Versus-Host Disease

9. Emerging Place of JAK Inhibitors in the Treatment of Inborn Errors of Immunity

10. Long term follow-up of pediatric-onset Evans syndrome: broad immunopathological manifestations and high treatment burden

11. Different Clinical Presentations and Outcomes of Disseminated Varicella in Children With Primary and Acquired Immunodeficiencies

12. Safety and efficacy of brentuximab vedotin as a treatment for lymphoproliferative disorders in primary immunodeficiencies

13. STING Gain-of-Function Disrupts Lymph Node Organogenesis and Innate Lymphoid Cell Development in Mice

14. Type I interferon-mediated autoinflammation due to DNase II deficiency

15. A web-based collection of genotype-phenotype associations in hereditary recurrent fevers from the Eurofever registry

16. Lymphadenopathy driven by TCR-Vγ8Vδ1 T-cell expansion in FAS-related autoimmune lymphoproliferative syndrome

17. Proceedings of the 23rd Paediatric Rheumatology European Society Congress: part one

18. Chronic Intestinal Pseudo-Obstruction and Lymphoproliferative Syndrome as a Novel Phenotype Associated With Tetratricopeptide Repeat Domain 7A Deficiency

19. JAK inhibition in Aicardi-Goutières syndrome: a monocentric multidisciplinary real-world approach study

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

21. Current Understanding and Future Research Priorities in Malignancy Associated With Inborn Errors of Immunity and DNA Repair Disorders: The Perspective of an Interdisciplinary Working Group

22. Human type I IFN deficiency does not impair B cell response to SARS-CoV-2 mRNA vaccination

23. Human kidney-derived hematopoietic stem cells can support long-term multilineage hematopoiesis

24. Use of eculizumab in children with allogeneic haematopoietic stem cell transplantation associated thrombotic microangiopathy-a multicentre retrospective PDWP and IEWP EBMT study

25. Copy number variations and founder effect underlying complete IL-10Rβ deficiency in Portuguese kindreds.

26. Mutations in the adaptor-binding domain and associated linker region of p110δ cause Activated PI3K-δ Syndrome 1 (APDS1)

27. Inherited TNFSF9 deficiency causes broad Epstein–Barr virus infection with EBV+ smooth muscle tumors

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

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

30. Monoclonal antibody-mediated neutralization of SARS-CoV-2 in an IRF9-deficient child

31. Hematopoietic Stem Cell Transplantation for Hepatitis-associated Aplastic Anemia Following Liver Transplantation for Nonviral Hepatitis: A Retrospective Analysis and a Review of the Literature by the Severe Aplastic Anemia Working Party of the European Society for Blood and Marrow Transplantation

32. EBMT/ESID inborn errors working party guidelines for hematopoietic stem cell transplantation for inborn errors of immunity

33. Single-cell analysis of FOXP3 deficiencies in humans and mice unmasks intrinsic and extrinsic CD4(+) T cell perturbations

34. Overview of STING-Associated Vasculopathy with Onset in Infancy (SAVI) Among 21 Patients

35. Diagnosis of autoimmune lymphoproliferative syndrome caused by FAS deficiency in adults

36. Differential Expression of Interferon-Alpha Protein Provides Clues to Tissue Specificity Across Type I Interferonopathies

37. Genomic spectrum and phenotypic heterogeneity of human IL-21 receptor deficiency

38. Preexisting autoantibodies to type I IFNs underlie critical COVID-19 pneumonia in patients with APS-1

39. CALR mutant protein rescues the response of MPL p.R464G variant associated with CAMT to eltrombopag

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

41. Improved outcome in children compared to adolescents and young adults after allogeneic hematopoietic stem cell transplant for acute myeloid leukemia: a retrospective study from the Francophone Society of Bone Marrow Transplantation and Cell Therapy (SFGM-TC)

42. Hematopoietic cell transplantation in chronic granulomatous disease: a study of 712 children and adults

43. β-Glucan–induced reprogramming of human macrophages inhibits NLRP3 inflammasome activation in cryopyrinopathies

44. Efficacy of ruxolitinib in subcutaneous panniculitis-like T-cell lymphoma and hemophagocytic lymphohistiocytosis

45. Hematopoietic Stem Cell Transplantation for Combined Immunodeficiencies, on Behalf of IEWP-EBMT

46. Long-term event-free survival, chimerism and fertility outcomes in 234 patients with sickle-cell anemia younger than 30 years after myeloablative conditioning and matched-sibling transplantation in France

47. Concomitant PIK3CD and TNFRSF9 deficiencies cause chronic active Epstein-Barr virus infection of T cells

48. Neurological Involvement in Childhood Evans Syndrome

49. The European Society for Immunodeficiencies (ESID) registry working definitions for the clinical diagnosis of inborn errors of immunity

50. Genetic diagnosis of primary immunodeficiencies: A survey of the French national registry

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