141 results on '"Gaspar, H B"'
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2. Author Correction: Long-term safety and efficacy of lentiviral hematopoietic stem/progenitor cell gene therapy for Wiskott–Aldrich syndrome
3. ADA Activity and dATP Levels in Erythrocytes after Bone Marrow Transplantation
4. Non-Myeloablative Stem Cell Transplantation for Congenital Immunodeficiencies
5. The Case for Mandatory Newborn Screening for Severe Combined Immunodeficiency (SCID)
6. Supplement to: A modified γ-retrovirus vector for X-linked severe combined immunodeficiency.
7. Current progress on gene therapy for primary immunodeficiencies
8. Impact of viral reactivations in the era of pre-emptive antiviral drug therapy following allogeneic haematopoietic SCT in paediatric recipients
9. Non-infectious Lung Disease in Patients with Adenosine Deaminase Deficient Severe Combined Immunodeficiency
10. Social outcome in children treated by haematopoietic cell transplant for congenital immunodeficiency
11. Allogeneic and autologous transplantation for haematological diseases, solid tumours and immune disorders: current practice in Europe 2009
12. Hematopoietic SCT in Europe: data and trends in 2012 with special consideration of pediatric transplantation
13. Progress and prospects: gene therapy for inherited immunodeficiencies
14. Allogeneic stem cell transplantation in X-linked lymphoproliferative disease: two cases in one family and review of the literature
15. Gene therapy progress and prospects: gene therapy for severe combined immunodeficiency
16. Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients
17. Familial haemophagocytic lymphohistiocytosis: advances in the genetic basis, diagnosis and management
18. Translational Mini-Review Series on Immunodeficiency: Molecular defects in common variable immunodeficiency
19. Non-Myeloablative Stem Cell Transplantation for Congenital Immunodeficiencies
20. Cutaneous Graft Versus Host Disease-Like Histopathological Features Following Gene Therapy
21. Prevalence of SAP gene defects in male patients diagnosed with common variable immunodeficiency
22. Pathology of astrovirus associated diarrhoea in a paediatric bone marrow transplant recipient
23. X-Linked lymphoproliferative disease: three atypical cases
24. Severe combined immunodeficiency—molecular pathogenesis and diagnosis
25. Kinase mutant Btk results in atypical X-linked agammaglobulinaemia phenotype
26. Early B cell defects
27. Bruton's tyrosine kinase expression and activity in X-linked agammaglobulinaemia (XLA): the use of protein analysis as a diagnostic indicator of XLA
28. Combined immunodeficiency due to JAK3 mutation in a child presenting with skin granuloma
29. Dock8 deficiency and a diagnostic score to differentiate it from other Hyper-IGE syndromes
30. Translational Mini-Review Series on Immunodeficiency: Molecular defects in common variable immunodeficiency
31. ADA Activity and dATP Levels in Erythrocytes after Bone Marrow Transplantation
32. Nonmyeloablative stem cell transplantation for congenital immunodeficiencies
33. Impact of viral reactivations in the era of pre-emptive antiviral drug therapy following allogeneic haematopoietic SCT in paediatric recipients
34. Biochemical and immunological status following gene therapy and PEG-ADA therapy for adenosine deaminase (ADA) deficiency
35. Current topic: Severe combined immunodeficiency---molecular pathogenesis and diagnosis
36. Short limbed skeletal dysplasia associated with combined immunodeficiency and congenital subglottic stenosis: a new constellation of features
37. IMMUNODEFICIENCY REVIEWEarly B cell defects
38. Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gammaretroviral vector
39. Pegademase bovine (PEG-ADA) for the treatment of infants and children with severe combined immunodeficiency (SCID)
40. Novel gene therapy strategies for ADA deficiency using AAV vectors or gene editing
41. A Modified γ-Retrovirus Vector for X-Linked Severe Combined Immunodeficiency.
42. Lentiviral vector mediated gene therapy for X-linked lymphoproliferative disease
43. Clinical and immunological features in a cohort of patients with partial DiGeorge syndrome followed at a single center
44. Combined immunodeficiency due to JAK3 mutation in a child presenting with skin granuloma
45. X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease
46. Progress and prospects: gene therapy clinical trials (part 1).
47. T cell suicide gene therapy to aid haematopoietic stem cell transplantation.
48. T cell transduction and suicide with an enhanced mutant thymidine kinase.
49. Defective expression of the interleukin-2/interleukin-15 receptor beta subunit leads to a natural killer cell-deficient form of severe combined immunodeficiency.
50. Cognitive and behavioral abnormalities in adenosine deaminase deficient severe combined immunodeficiency.
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