556 results on '"Le Deist, F."'
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2. Acceptability Conditions for Telemonitoring Gerontechnology in the Elderly: Optimising the Development and Use of This New Technology
3. Severe Combined Immunodeficiencies in Humans
4. Leukocyte Adhesion Deficiency as a Model for the Study of the Functional Role of LFA-1
5. Reconstitution of maturating and regulatory lymphocyte subsets after cord blood and BMT in children
6. Impact of HLA matching on outcome of hematopoietic stem cell transplantation in children with inherited diseases: a single-center comparative analysis of genoidentical, haploidentical or unrelated donors
7. LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1
8. SIAH-1 inhibits cell growth by altering the mitotic process
9. Plasmacytoid dendritic cell reconstitution is faster after cord blood than after bone marrow transplantation: P747
10. Bone marrow transplantation as treatment for X-linked immunodeficiency with hyper-IgM
11. Stem cell transplantation for immunodeficiency
12. Syndrome d'Evans : étude rétrospective de la société d'hématologie et d'immunologie pédiatrique (36 cas)
13. Déficit de l’immunité antivirale : EBV, CMV, adénovirus
14. Transient familial haemophagocytic lymphohistiocytosis reactivation post-CD34 haematopoietic stem cell transplantation
15. Coombsʼ negative haemolytic anaemia as a first manifestation of autoimmune lymphoproliferative disease
16. Where do we stand 6 years after gene therapy?
17. Mutations in Fas Associated with Human Lymphoproliferative Syndrome and Autoimmunity
18. X-linked thrombocytopenia and Wiskott-Aldrich syndrome: similar regional assignment but distinct X-inactivation pattern in carriers
19. Comment explorer un déficit immunitaire?
20. Cytomegalovirus infection in infants with autoimmune lymphoproliferative syndrome (ALPS)
21. Prevention of EBV-induced B-lymphoproliferative disorder by ex vivo marrow B-cell depletion in HLA-phenoidentical or non-identical T-depleted bone marrow transplantation
22. thérapie génique des déficits immunitaires
23. RESTRICTED T-CELL Vβ REPERTOIRE DIVERSITY IN PERIPHERAL BLOOD AND TISSUE INFILTRATING LYMPHOCYTES IN OMENN'S SYNDROME (SEVERE COMBINED IMMUNODEFICIENCY WITH ERYTHRODERMA AND HYPEREOSINOPHILIA)
24. Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization
25. Treatment of Omenn syndrome by bone marrow transplantation
26. Increased Radiosensitivity of Granulocyte Macrophage Colony-forming Units and Skin Fibroblasts in Human Autosomal Recessive Severe Combined Immunodeficiency
27. Défauts génétiques du contrôle de l'activation T évoluant vers un syndrome d'activation lymphohistiocytaire
28. The Role of PGE2 in the Induction of Suppressor Cells in Humans
29. The Leukocyte Adhesion Deficiency
30. Is Xenotransplantation of Embryonic Stem Cells a Realistic Option?
31. Impaired T8 lymphocyte-mediated suppressive activity in patients with partial Di George syndrome
32. Activation of genetically major histocompatibility complex (MHC) class II-deficient B lymphocytes
33. Effects of interferon-γ (IFN-γ) and tumor necrosis factor-α (TNF-α) on the expression of LFA-1 in the moderate phenotype of leukocyte adhesion deficiency (LAD)
34. Mannan-specific and mannan-induced T-cell suppressive activity in patients with chronic mucocutaneous candidiasis
35. Munc13-4, un nouvel effecteur indispensable à la sécrétion des granules cytotoxiques
36. Donor T lymphocyte infusion following ex vivo depletion of donor anti-host reactivity by a specific anti–interleukin-2 receptor P55 chain immunotoxin
37. PROSPECTIVE STUDY OF THE OCCURRENCE OF MONOCLONAL GAMMAPATHIES FOLLOWING BONE MARROW TRANSPLANTATION IN YOUNG CHILDREN
38. Long-term outcome following hematopoietic stem cell transplantation in Wiskott-Aldrich syndrome: collaborative study of the European Society for Immunodeficiencies and the European Group for Blood and Marrow Transplantation
39. Cernunnos, a novel V(D)J recombination /non homologus end-joining factor, is mutated in human T and B cell immunodeficiency associated with microcephaly
40. Autoimmune lymphoproliferative syndrome and perforin
41. P-102: Bioavailability and tolerance of high doses vitamin D in children with newly diagnosed Crohn’s disease
42. A hypermorphic I kappa B alpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency
43. A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency
44. Low penetrance, broad resistance, and favorable outcome of interleukin 12 receptor beta 1 deficiency: Medical and immunological implications
45. Low penetrance, broad resistance, and favorable outcome of interleukin 12 receptor ß1 deficiency: Medical and immunological implications
46. Autoimmune lymphoproliferative syndromes (ALPS): models for the study of peripheral tolerance
47. Gene therapy of severe combined immunodeficiencies
48. Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome
49. Treatment of familial hemophagocytic lymphohistiocytosis with bone marrow transplantation from HLA genetically nonidentical donors
50. Mutations hypomorphiques de RAG1 et infections à CMV : un nouveau phénotype de déficit immunitaire
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