459 results on '"Caillat-Zucman S"'
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2. Topic: AS06-Prognosis/AS06a-Prognostic factors of outcome and risk assessment: APPLICABILITY OF IPSS-M IN MYELODYSPLASTIC SYNDROMES ARISING FROM APLASTIC ANEMIA AND PAROXYSMAL NOCTURNAL HEMOGLOBINURIA
3. P087 - Topic: AS06-Prognosis/AS06a-Prognostic factors of outcome and risk assessment: APPLICABILITY OF IPSS-M IN MYELODYSPLASTIC SYNDROMES ARISING FROM APLASTIC ANEMIA AND PAROXYSMAL NOCTURNAL HEMOGLOBINURIA
4. Factors associated with the presence of glutamic acid decarboxylase and islet antigen-2 autoantibodies in patients with long-standing type 1 diabetes
5. Is there any impact of HLA-DPB1 disparity in 10/10 HLA-matched unrelated hematopoietic SCT? Results of a French multicentric retrospective study
6. Acute generalized exanthematous pustulosis induced by hydroxychloroquine prescribed for COVID-19
7. Association of PTPN22+1858C/T polymorphism with Type 1 diabetes in the North Indian population
8. 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
9. Essai de phase 2 multicentrique évaluant le pembrolizumab dans la maladie de Kaposi classique ou endémique
10. Les auteurs
11. Histological features and HLA class II alleles in hepatitis C virus chronically infected patients with persistently normal alanine aminotransferase levels. (Liver Disease)
12. 1077MO PD1 blockade with pembrolizumab in classic and endemic Kaposi sarcoma: A multicenter phase II study
13. Surfaces and equipment contamination by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in the emergency department at a university hospital
14. Acute generalized exanthematous pustulosis induced by hydroxychloroquine prescribed for COVID-19
15. Molecular mechanisms of HLA association with autoimmune diseases
16. Relative predispositional effects of HLA class II DRB1-DQB1 haplotypes and genotypes on type 1 diabetes: a meta-analysis
17. Does haploidentical transplantation in children with primary immunodeficiencies have the potential to exploit donor NK cell alloreactivity?
18. The Extent and Differentiation Phenotype of HHV8-Specific CD8 T Cells are Associated with Spontaneous Control of Infection and Absence of Kaposi sarcoma
19. Transient familial haemophagocytic lymphohistiocytosis reactivation post-CD34 haematopoietic stem cell transplantation
20. Islet cell antibody heterogeneity among Type 1 (insulin-dependent) diabetic patients
21. Rationale for a T Cell Receptor Peptide Therapy in Myasthenia Gravis
22. HLA-B phenotype modifies the course of Behçetʼs disease in Moroccan patients
23. Sjögren syndrome: an unexpected disease occurring fourteen years after oligoarticular onset juvenile idiopathic arthritis
24. HLA class I polymorphism in a Moroccan population from Casablanca
25. Anticardiolipin antibodies in patients with multiple sclerosis do not represent a subgroup of patients according to clinical, familial, and biological characteristics
26. Lack of evidence of a specific role for C4A gene deficiency in determining disease susceptibility among C4-deficient patients with systemic lupus erythematosus (SLE)
27. Linkage and association study of the CTLA-4 region in coeliac disease for Italian and Tunisian populations
28. PS943 SAFETY AND EFFICACY OF TISAGENLECLEUCEL (CTL019) IN B ACUTE LYMPHOBLASTIC LEUKEMIA IN CHILDREN AND YOUNG ADULTS: ROBERT DEBRÉ AND SAINT LOUIS HOSPITALS EXPERIENCE
29. Distinctive effects of CCR5, CCR2, and SDF1 genetic polymorphisms in AIDS progression
30. CTLA-4 gene polymorphism is associated with predisposition to coeliac disease
31. HLA class II allele and haplotype distribution in a population from central Poland
32. IDENTIFICATION OF PEPTIDES FROM AUTOANTIGENS GAD65 AND IA-2 BINDING TO HLA CLASS II MOLECULES PREDISPOSING FOR AND PROTECTING FROM IDDM
33. A NEW PREDICTIVE MODEL FOR IDDM SUSCEPTIBILITY BASED ON MOLECULAR FEATURES OF HLA DRB1/DQB1. A WORLD WIDE STUDY OF 1166 PATIENTS
34. FUNCTION OF TAPASIN ANALYZED BY CO-EXPRESSION WITH TAP, HLA CLASS I MOLECULES AND CHAPERONES CALRETICULIN AND CALNEXIN IN SF9 INSECT CELLS
35. MECHANISM OF SUBSTRATE TRANSLOCATION BY ABC TRANSPORTERS: ROLE OF ATP AND CONFORMATIONAL CHANGES FOR PEPTIDE TRANSPORT BY TAP COMPLEXES ANALYZED BY SITE DIRECTED MUTAGENESIS
36. HLA class II DNA polymorphism in a Moroccan population from the Souss, Agadir area
37. Linkage disequilibrium between HLA class II (DR, DQ, DP) and antigen processing (LMP, TAP, DM) genes of the major histocompatibility complex
38. Rôle des cellules MAIT dans le contrôle de la tuberculose de l’enfant
39. New insights into the understanding of MHC associations with immune-mediated disorders
40. NCR3/NKp30 contributes to pathogenesis in primary Sj\xf6gren\u2019s syndrome
41. Expression of NKG2D and CD107 in CD8(+) effector memory lymphocytes in Churg-Stauss syndrome
42. Early post-transplant donor-derived invariant natural killer T cell recovery predicts the occurrence of acute graft-versus-host disease and overall survival
43. Prix SFP 2013 – 4 – Reconstitution des MAIT après allogreffe de cellules souches hématopoïétiques chez l'enfant
44. O-064 Development And Maturation Of Mait Cells In Human Neonates: Relations With Gestational Age And Microbial Infection
45. New insights into the understanding of MHC associations with immune-mediated disorders.
46. Structural analysis of two HLA-DR-presented autoantigenic epitopes: crucial role of peripheral but not central peptide residues for T-cell receptor recognition
47. Absence of functional relevance of human transporter associated with antigen processing polymorphism for peptide selection
48. Controversies about the histological features of chronic HCV patients with persistently normal alanine transaminase levels: What can be done about the present definition?
49. P214 Persistance à long terme des anticorps anti-GAD et anti-IA-2 au cours du diabète de type 1 (DT1)
50. Un nouveau mécanisme d’échappement du VHC à la réponse immune : l’inhibition des fonctions cytotoxiques des cellules NK par la protéine NS5A via l’induction de la sécrétion monocytaire d’interleukine 10 et de TGFβ
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