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2. Severe and fatal forms of COVID-19 in children

4. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

6. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

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

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

9. Autoantibodies against type I IFNs in patients with life-threatening COVID-19

10. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

12. Spectrométrie de fluorescence des rayons X portable quantification, imagerie, où en est-on ? Instrumentation portable : Quels enjeux pour l'archéométrie ?

13. Haploidentical Hematopoietic Stem Cell Transplantation with Post-Transplant Cyclophosphamide for Primary Immunodeficiencies and Inherited Disorders in Children

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

23. Dupilumab in atopic-dermatitis-like eczema associated with inborn errors of immunity: a nationwide study.

25. Somatic RAP1B gain-of-function variant underlies isolated thrombocytopenia and immunodeficiency.

26. Efficacy of eculizumab in transplantation-associated thrombotic microangiopathy: results of the French nationwide study on behalf of the SFGM-TC and the CNR-MAT.

27. Pediatric refractory chronic immune thrombocytopenia: Identification, patients' characteristics, and outcome.

28. Ovarian tissue cryopreservation for fertility preservation before hematopoietic stem cell transplantation in patients with sickle cell disease: safety, ovarian function follow-up, and results of ovarian tissue transplantation.

29. Pediatric intracranial empyema complicating otogenic and sinogenic infection.

30. On behalf of the SFGM-TC: Real-life use of third-party virus-specific T-cell transfer in immunocompromised transplanted patients.

31. JAK inhibitor treatment for inborn errors of JAK/STAT signaling: An ESID/EBMT-IEWP retrospective study.

32. Letermovir for CMV Prophylaxis in Very High-Risk Pediatric Hematopoietic Stem Cell Transplantation Recipients for Inborn Errors of Immunity.

33. Recent results of hematopoietic stem cell transplantation for thalassemia with busulfan-based conditioning regimen in France: improved thalassemia free survival despite frequent mixed chimerism. A retrospective study from the Francophone Society of Stem Cell Transplantation and Cellular Therapy (SFGM-TC).

34. Impact of Graft Function on Health Status and Quality of Life in Very Long-Term Survivors Who Received an HSCT for Inborn Errors of Immunity, a Prospective Study of the CEREDIH.

35. HLA haplotype frequencies and diversity in patients with hemoglobinopathies.

36. JAK Inhibition in Aicardi-Goutières Syndrome: a Monocentric Multidisciplinary Real-World Approach Study.

37. DOCK11 deficiency in patients with X-linked actinopathy and autoimmunity.

38. Late-onset enteric virus infection associated with hepatitis (EVAH) in transplanted SCID patients.

39. Genetic Diagnosis Guides Treatment of Autoimmune Enteropathy.

40. Long term follow-up after haematopoietic stem cell transplantation for mucopolysaccharidosis type I-H: a retrospective study of 51 patients.

41. Deficiency of the minor spliceosome component U4atac snRNA secondarily results in ciliary defects in human and zebrafish.

42. Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency.

43. [Inborn error of metabolism and allogenic hematopoietic cell transplantation: Guidelines from the SFGM-TC].

45. HLA-matched related donor hematopoietic stem cell transplantation is a suitable treatment in adolescents and adults with sickle cell disease: Comparison of myeloablative and non-myeloablative approaches.

46. Inherited TNFSF9 deficiency causes broad Epstein-Barr virus infection with EBV+ smooth muscle tumors.

47. Bayesian Modeling Immune Reconstitution Apply to CD34+ Selected Stem Cell Transplantation for Severe Combined Immunodeficiency.

48. Monoclonal antibody-mediated neutralization of SARS-CoV-2 in an IRF9-deficient child.

49. Two Novel Homozygous Mutations in Phosphoglucomutase 3 Leading to Severe Combined Immunodeficiency, Skeletal Dysplasia, and Malformations.

50. Sustained remission after haploidentical bone marrow transplantation in a child with refractory systemic juvenile idiopathic arthritis.

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