788 results on '"Griscelli, C."'
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2. Close Linkage of the Locus for X Chromosome-Linked Severe Combined Immunodeficiency to Polymorphic DNA Markers in Xq11-q13
3. Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27β
4. X-linked thrombocytopenia and Wiskott-Aldrich syndrome: similar regional assignment but distinct X-inactivation pattern in carriers
5. European experience of bone-marrow transplantation for severe combined immunodeficiency
6. Skin lesions revealing neonatal acute leukemias with monocytic differentiation. A report of 3 cases
7. Treatment of Omenn syndrome by bone marrow transplantation
8. Interferon Gamma for Chronic Granulomatous Disease
9. Hl-A Antigens And Immune Deficiency States
10. The Role of PGE2 in the Induction of Suppressor Cells in Humans
11. Self Education after Mismatched HLA Haploidentical Bone Marrow Transplantation
12. A Second Case of Inosine Phosphorylase Deficiency with Severe T-Cell Abnormalities
13. Monoclonal Antibodies Specific for Human and Rat Intestinal Lymphocytes
14. Complete Adenosine Deaminase (ADA) Deficiency without Immunodeficiency, and Primary Hyperoxaluria, in a 12-Year-Old Boy
15. Intermediate-Risk Childhood Acute Lymphoblastic Leukemias: Amsacrine + Cytosine Arabinoside Versus Intermediate-Dose Methotrexate for Consolidation, and 6-Mercaptopurine + Methotrexate + Vincristine Versus Monthly Pulses for Maintenance
16. Transplantation of Lymphoid Cells in Patients with Severe Combined Immunodeficiency (SCID)
17. Transplantation of Lymphoid Cells in Patients with Severe Combined Immunodeficiency (SCID)
18. Transfer Factor Therapy in Immunodeficiencies
19. Severe combined immunodeficiency with B lymphocytes: a selective defect of precursor T cells
20. Das Hyper-IgE-Syndrom (Buckley- oder Hiob-Syndrom)
21. Das Wiskott-Aldrich Syndrom
22. Defect of Expression of MHC Genes Responsible for an Abnormal HLA Class I Phenotype and the Class II Negative Phenotype of Lymphocytes from Patients with Combined Immunodeficiency
23. Migration, Recirculation and Transformation of Large Dividing Lymph Node Cells in Syngeneic Recipient Rats Following Intravenous Injection
24. France
25. Impaired T8 lymphocyte-mediated suppressive activity in patients with partial Di George syndrome
26. Das Buckley-Syndrom: Rezidivierende, schwere Staphylokokken-infektionen, Ekzem und Hyperimmunglobulinämie E
27. Biotin-responsive immunoregulatory dysfunction in multiple carboxylase deficiency
28. Xp21 DNA microdeletion in a patient with chronic granulomatous disease, retinitis pigmentosa, and McLeod phenotype
29. Activation of genetically major histocompatibility complex (MHC) class II-deficient B lymphocytes
30. 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)
31. Hypoglycaemia induced by antibodies to insulin receptor following a bone marrow transplantation in an immunodeficient child
32. Mannan-specific and mannan-induced T-cell suppressive activity in patients with chronic mucocutaneous candidiasis
33. Monoclonal Antibodies Specific for Human and Rat Intestinal Lymphocytes
34. Transfer Factor Therapy in Immunodeficiencies
35. Self/Non Self Education and HLA-Restricted Cell Cooperation After Haploidentical Bone Marrow Transplantation
36. Transplantation of Lymphoid Cells in Patients with Severe Combined Immunodeficiency (SCID)
37. HLA Mismatched Bone Marrow Transplantation for Severe Combined Immunodeficiency and Other Non Malignant Disorders
38. EFFETS DE L'ISOPRINOSINE SUR L'ACTIVATION DE LYMPHOCYTES HUMAINS IN VITRO
39. Intermediate-Risk Childhood Acute Lymphoblastic Leukemias: Amsacrine + Cytosine Arabinoside Versus Intermediate-Dose Methotrexate for Consolidation, and 6-Mercaptopurine + Methotrexate + Vincristine Versus Monthly Pulses for Maintenance
40. New data on clonal anomalies of chromosome 14 in ataxia telangiectasia: tct (14;14) and inv(14)
41. Close linkage of random DNA fragments from Xq 21.3–22 to X-linked agammaglobulinaemia (XLA)
42. Tandem translocation t(14;14) in isolated and clonal cells in ataxia telangiectasia are different
43. Chediak-Higashi Syndrome I: Biochemical Abnormality and Prospects for Prenatal Diagnosis1
44. Detection of HIV1 DNA in infants and children by means of the polymerase chain reaction
45. Self/Non Self Education and HLA-Restricted Cell Cooperation After Haploidentical Bone Marrow Transplantation
46. Treatment of Severe Epstein-Barr Virus-Induced Polyclonal B-Lymphocyte Proliferation by Anti-B-Cell Monoclonal Antibodies: Two Cases After HLA-Mismatched Bone Marrow Transplantation
47. Functional T cell immunodeficiency characterized by defective TCR/CD3 induced tyrosylphosphorylation
48. A retrospective single-center study of clinical presentation and outcome in 117 patients with severe combined immunodeficiency
49. NF-X, a transcription factor implicated in MHC class II gene regulation
50. Polymerase chain reaction for studies of mother to child transmission of HIV1 in Africa
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