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3. Hereditary C1q Deficiency is Associated with Type 1 Interferon-Pathway Activation and a High Risk of Central Nervous System Inflammation

4. Childhood Langerhans cell histiocytosis hematological involvement: severity associated with BRAFV600E loads

5. Interleukin (IL)-1/IL-6-Inhibitor–Associated Drug Reaction With Eosinophilia and Systemic Symptoms (DReSS) in Systemic Inflammatory Illnesses

6. French protocol for the diagnosis and management of systemic lupus erythematosus

9. Antinuclear antibody–associated autoimmune cytopenia in childhood is a risk factor for systemic lupus erythematosus

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

12. Severe adult hemophagocytic lymphohistiocytosis (HLHa) correlates with HLH-related gene variants

13. Hyper inflammatory syndrome following COVID-19 mRNA vaccine in children: A national post-authorization pharmacovigilance study

14. Early systemic inflammation induces neurodevelopmental disorders: results from ARTEMIS, a French multicenter study of juvenile rheumatisms and systemic autoimmune and auto-inflammatory disorders and meta-analysis

15. Juvenile Neuropsychiatric Systemic Lupus Erythematosus: Identification of Novel Central Neuroinflammation Biomarkers

17. Criteria Associated with Treatment Decisions in Juvenile Idiopathic Arthritis with a Focus on Ultrasonography: Results from the JIRECHO Cohort

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

19. Iron Deficiency in Familial Mediterranean Fever: A Study on 211 Adult Patients From the JIR Cohort.

20. Curation and expansion of Human Phenotype Ontology for defined groups of inborn errors of immunity

23. A monocyte/dendritic cell molecular signature of SARS-CoV-2-related multisystem inflammatory syndrome in children with severe myocarditis

24. COVID-19 outcomes in patients with inflammatory rheumatic and musculoskeletal diseases treated with rituximab: a cohort study

25. Overview of STING-Associated Vasculopathy with Onset in Infancy (SAVI) Among 21 Patients

26. Mevalonate Kinase Deficiency

28. TIF1-gamma IgG2 isotype is not associated with malignancy in juvenile dermatomyositis patients.

29. A diagnostic dilemma in a boy with lupus and dyspnea: Answers

31. Differential Expression of Interferon-Alpha Protein Provides Clues to Tissue Specificity Across Type I Interferonopathies

32. Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohorts

34. Monogenic lupus: Dissecting heterogeneity

37. Juvenile neuropsychiatric systemic lupus erythematosus: A specific clinical phenotype and proposal of a probability score

38. Antinuclear antibodies associated auto-immune cytopenia in childhood is a risk factor for systemic lupus erythematosus

39. Clinical, histological, immunological presentations and outcomes of bullous systemic lupus erythematosus: 10 New cases and a literature review of 118 cases

41. Blau Syndrome–Associated Uveitis: Preliminary Results From an International Prospective Interventional Case Series

43. IFN-β plasmatic levels are best predictors of muscle disease activity than IFN-α in a longitudinal cohort of patients with juvenile dermatomyositis

44. Targeting the chemokine receptor CXCR4 with histamine analog to reduce inflammation in juvenile arthritis

45. Functional diversity ofNLRP3gain-of-function mutants associated with CAPS autoinflammation

47. Curation and expansion of the Human Phenotype Ontology for systemic autoinflammatory diseases improves phenotype-driven disease-matching

48. Severe adult hemophagocytic lymphohistiocytosis (HLHa) correlates with HLH-related gene variants

49. Autoimmune and inflammatory manifestations occur frequently in patients with primary immunodeficiencies

50. Familial and syndromic lupus share the same phenotype as other early-onset forms of lupus

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