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126 results on '"Dion, Jérémie"'

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1. Neurological manifestations in patients with VEXAS syndrome

2. Green Central Banking

4. A role for IL-33-activated ILC2s in eosinophilic vasculitis

6. A Clinicopathological Description of Kidney Features in VEXAS Syndrome

8. Osteitis in Systemic Sclerosis: A Nationwide Case–Control Retrospective Study

11. The CARMEN-France registry of adult patients with immune thrombocytopenia and autoimmune hemolytic anemia in France

12. Sotrovimab therapy elicits antiviral activities against Omicron BQ.1.1 and XBB.1.5 in sera of immunocompromised patients

13. Sotrovimab therapy elicits antiviral activities against Omicron BQ.1.1 and XBB.1.5 in sera of immunocompromised patients

15. Induction failure in granulomatosis with polyangiitis: a nationwide case-control study of risk factors and outcomes

19. Reply

22. Autoantibodies versus Skin Fibrosis Extent in Systemic Sclerosis: A Case-Control Study of Inverted Phenotypes

23. Reply

24. Green Central Banking

25. Central Banking and Inequalities: Old Tropes and New Practices

26. Systemic inflammatory and autoimmune manifestations associated with myelodysplastic syndromes and chronic myelomonocytic leukaemia: a French multicentre retrospective study

28. Osteitis in Systemic Sclerosis: a nationwide case-control retrospective study (SCLEROS Study)

29. Serious Infections in Patients with Vexas Syndrome: A Study from the French Vexas Group

30. Autoimmune Cytopenia Associated with Indolent B-Cell Clones: A Large Multicentric Cohort Study

31. Whole Exome Sequencing of Patients with Adult-Onset Evans Syndrome: A Cohort of 80 Patients

32. Rituximab plus methotrexate combination as a salvage therapy in persistently active granulomatosis with polyangiitis.

33. Campylobacter infection in adult patients with primary antibody deficiency

34. Autorégulation épistémique des systèmes sociaux de production de connaissance: le cas de la Banque du Canada

36. Skewed peripheral B- and T-cell compartments in patients with ANCA-associated vasculitis.

38. Campylobacter infection in adult patients with primary antibody deficiency

42. Relapsing polychondritis can be characterized by three different clinical phenotypes: analysis of a recent series of 142 patients

44. Systemic inflammatory and autoimmune manifestations associated with myelodysplastic syndromes and chronic myelomonocytic leukaemia: a French multicentre retrospective study

48. Hypereosinophilia and Hypereosinophilic Syndromes: First Findings From a Nationwide Multicenter Cohort.

49. Splinter haemorrhages, splenic infarcts, and pulmonary embolism in granulomatosis with polyangiitis.

50. Presentation, Diagnosis, and Management of Subglottic and Tracheal Stenosis During Systemic Inflammatory Diseases

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