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Munchausen by proxy syndrome mimicking systemic autoinflammatory disease: case report and review of the literature.Development of positive antinuclear antibodies and rheumatoid factor in systemic juvenile idiopathic arthritis points toward an autoimmune phenotype later in the disease course.Effectiveness of dexamethasone iontophoresis for temporomandibular joint involvement in juvenile idiopathic arthritis.B-cell depletion in Wegener's granulomatosis.Treatment with high-dose recombinant human hyaluronidase-facilitated subcutaneous immune globulins in patients with juvenile dermatomyositis who are intolerant to intravenous immune globulins: a report of 5 cases.Gene expression signatures in polyarticular juvenile idiopathic arthritis demonstrate disease heterogeneity and offer a molecular classification of disease subsets.Subtype-specific peripheral blood gene expression profiles in recent-onset juvenile idiopathic arthritis.Rituximab therapy for severe refractory chronic Henoch-Schönlein purpura.Management of juvenile idiopathic arthritis: hitting the target.Challenges of Diagnosing Cognitive Dysfunction With Neuropsychiatric Systemic Lupus Erythematosus in Childhood.Correlation of Secretory Activity of Neutrophils With Genotype in Patients With Familial Mediterranean Fever.Kawasaki disease without fever.Single amino acid charge switch defines clinically distinct proline-serine-threonine phosphatase-interacting protein 1 (PSTPIP1)-associated inflammatory diseases.4.4 Different phenotype of anaemia in systemic juvenile idiopathic arthritis (s-JIA) compared to anaemia in other subtypes of JIA.PW02-018 - Impact of PSTPIP1 mutaions on clinical phenotype.Evaluation of sedimentation rate methodology reveals an unusual pediatric subpopulation with lupus or lupus-like syndrome and hemolytic anemia.Reply to du Moulin et al.: Cerebral vasculopathy is a common hallmark in individuals with SAMHD1 mutations.Understanding the biology and use of TNF therapy in jia-clinical outcomes.Proinflammatory Cytokine Environments Can Drive Interleukin-17 Overexpression by γ/δ T Cells in Systemic Juvenile Idiopathic Arthritis.Practice and consensus-based strategies in diagnosing and managing systemic juvenile idiopathic arthritis in Germany.Combination of ofatumumab and fresh frozen plasma in hypocomplementemic systemic lupus erythematosus: a case report.Varicella-zoster-virus vaccination in immunosuppressed children with rheumatic diseases using a pre-vaccination check list.Autoinflammatory diseases: New diagnostic criteria for CAPS - turning horses into zebras?Current management of juvenile dermatomyositis in Germany and Austria: an online survey of pediatric rheumatologists and pediatric neurologists.Development of practice and consensus-based strategies including a treat-to-target approach for the management of moderate and severe juvenile dermatomyositis in Germany and Austria.Inherited p40phox deficiency differs from classic chronic granulomatous diseaseB cell depletion: on the risePediatric rheumatology--its own specialtyLeukocyte adhesion deficiency type 1 presenting with recurrent pyoderma gangrenosum and flaccid scarringCombination of rituximab and abatacept as an exit strategy for repetitive B-cell depletion in children with severe autoimmune diseases: a report of three casesCalcium and zinc tune autoinflammatory Toll-like receptor 4 signaling by S100A12Impact of IL1RN Variants on Response to Interleukin-1 Blocking Therapy in Systemic Juvenile Idiopathic Arthritis[Back to school physical education despite rheumatism : Development and testing of a sport scientific-based physical education certification]Synergistic Signaling of TLR and IFNα/β Facilitates Escape of IL-18 Expression from Endotoxin ToleranceSerum S100A8/A9 and S100A12 Levels in Children With Polyarticular Forms of Juvenile Idiopathic Arthritis: Relationship to Maintenance of Clinically Inactive Disease During Anti-Tumor Necrosis Factor Therapy and Occurrence of Disease Flare After DiscReply
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