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143 results on '"Aiuti Alessandro"'

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

2. Gene therapy for Wiskott-Aldrich syndrome: History, new vectors, future directions

3. Consensus approach for the management of severe combined immune deficiency caused by adenosine deaminase deficiency.

4. Autonomous role of Wiskott-Aldrich syndrome platelet deficiency in inducing autoimmunity and inflammation

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

6. Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders

7. B-cell development and functions and therapeutic options in adenosine deaminase–deficient patients

8. The Wiskott-Aldrich syndrome protein is required for iNKT cell maturation and function

9. WASP regulates suppressor activity of human and murine CD4+CD25+FOXP3+ natural regulatory T cells

10. Activated Phosphoinositide 3-Kinase δ Syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity

11. Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia

12. 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. Decoding the Human Genetic and Immunological Basis of COVID-19 mRNA Vaccine-Induced Myocarditis

14. Autoantibodies against type I IFNs in patients with critical influenza pneumonia

15. Vaccine breakthrough hypoxemic COVID-19 pneumonia in patients with auto-Abs neutralizing type I IFNs

16. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

17. X-linked recessive TLR7 deficiency in similar to 1% of men under 60 years old with life-threatening COVID-19

18. SARS-CoV-2-related MIS-C:A key to the viral and genetic causes of Kawasaki disease?

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

21. In vivo tracking of T cells in humans unveils decade-long survival and activity of genetically modified T memory stem cells

22. Altered B cell development and fuctions in Adenosine Deaminase deficient patients

23. Auto-antibodies against type I IFNs in patients with life-threatening COVID-19

24. A Case of Two Adult Brothers with Wiskott-Aldrich Syndrome, One Treated with Gene Therapy and One with HLA-Identical Hematopoietic Stem Cell Transplantation

25. Natural history of type 1 diabetes on an immunodysregulatory background with genetic alteration in B-cell activating factor receptor: A case report

26. Radiosensitivity in patients affected by ARPC1B deficiency: a new disease trait?

27. Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency

28. The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet)

29. Consensus approach for the management of severe combined immune deficiency caused by adenosine deaminase deficiency

30. Reduced Follicular Regulatory T Cells in Spleen and Pancreatic Lymph Nodes of Patients With Type 1 Diabetes

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

32. A Prevalent CXCR3+ Phenotype of Circulating Follicular Helper T Cells Indicates Humoral Dysregulation in Children with Down Syndrome

33. Consensus of the Italian Primary Immunodeficiency Network on transition management from pediatric to adult care in patients affected with childhood-onset inborn errors of immunity

34. New perspectives in gene therapy for inherited disorders

35. Severe Toxoplasma gondii infection in a member of a NFKB2-deficient family with T and B cell dysfunction

36. Neonatal umbilical cord blood transplantation halts skeletal disease progression in the murine model of MPS-I

37. The case of an APDS patient: Defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment

38. Gene therapy for ADA‐SCID, the first marketing approval of an ex vivo gene therapy in Europe: paving the road for the next generation of advanced therapy medicinal products

39. Bone marrow–derived CD34 − fraction: A rich source of mesenchymal stromal cells for clinical application

40. Corrigendum: Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies

41. Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies

42. Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network

43. ALPS-Like Phenotype Caused by ADA2 Deficiency Rescued by Allogeneic Hematopoietic Stem Cell Transplantation

44. The Role of Conditioning in Hematopoietic Stem-Cell Gene Therapy

45. Lentiviral Vector Gene Therapy Protects XCGD Mice From Acute Staphylococcus aureus Pneumonia and Inflammatory Response

46. Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry

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

48. Autonomous role of Wiskott-Aldrich Syndrome platelet deficiency in inducing autoimmunity and inflammation

49. Circulating follicular helper and follicular regulatory T cells are severely compromised in human CD40 deficiency: A case report

50. Use of Defibrotide to help prevent post-transplant endothelial injury in a genetically predisposed infant with metachromatic leukodystrophy undergoing hematopoietic stem cell gene therapy

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