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Aktueller Newsletter

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April

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  • Partial clinical response to anakinra in severe palmoplantar pustular psoriasis.
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  • Periodic fever, aphthous stomatitis, pharyngitis and cervical adenopathy syndrome is associated with activation of GM-CSF and burst-like expression of IL-8 in peripheral blood.
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  • A pro-inflammatory signalome is constitutively activated by C33Y mutant TNF receptor 1 in TNF receptor-associated periodic syndrome (TRAPS).
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  • Tumor necrosis factor receptor-associated periodic syndrome managed with the couple canakinumab-alendronate.
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  • Interleukin 6 blockade for hyperimmunoglobulin D and periodic fever syndrome.
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  • Cryopyrin associated periodic syndrome with neurological involvement in a 50-year-old patient.
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  • Muckle wells syndrome associated with multifocal clinically isolated syndrome.
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  • Successful treatment of Schnitzler syndrome with cyclosporine.
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  • Drug survival and reasons for discontinuation of the first course of biological therapy in 301 juvenile idiopathic arthritis patients.
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  • Bone mass and quality in patients with juvenile idiopathic arthritis: longitudinal evaluation of bone mass determinants using dual energy X-ray absorptiometry, peripheral quantitative computed tomography, and quantitative ultrasonography.
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  • An Unusual Case of Adult-Onset Still's Disease with Hemophagocytic Syndrome, Necrotic Leukoencephalopathy and Disseminated Intravascular Coagulation.
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  • Adult-onset still disease: manifestations, treatment, outcome, and prognostic factors in 57 patients.
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  • Rituximab for refractory adult-onset Still's disease with thrombotic microangiopathy.
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  • Erratum to: Refractory urticaria in adult-onset Still's disease.
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  • A novel therapeutic approach in pulmonary arterial hypertension as a complication of adult-onset Still's disease: targeting IL-6.
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  • Cardiac magnetic resonance in myocarditis from adult onset Still's disease successfully treated with anakinra.
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  • Neutrophil-Lymphocyte Ratio in Patients With Familial Mediterranean Fever.
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  • Two elderly cases of familial mediterranean fever with rheumatoid arthritis.
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  • Protracted Febrile Myalgia Syndrome in a Kidney Transplant Recipient With Familial Mediterranean Fever.
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  • Assessment of sleep problems in children with familial Mediterranean fever.
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  • Amyloid A amyloidosis in a Japanese patient with familial Mediterranean fever associated with homozygosity for the pyrin variant M694I/M694I.
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Februar

  • Mevalonate kinase deficiency in two sisters with therapeutic response to anakinra: case report and review of the literature.
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  • Renal involvement in secondary amyloidosis of Muckle-Wells syndrome: marked improvement of renal function and reduction of proteinuria after therapy with human anti-interleukin-1β monoclonal antibody canakinumab.
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  • Defects in mitochondrial clearance predispose human monocytes to interleukin-1β hypersecretion.
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  • CARD8 is a negative regulator for NLRP3 inflammasome, but mutant NLRP3 in cryopyrin-associated periodic syndromes escapes the restriction.
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  • Renal involvement in secondary amyloidosis of Muckle-Wells syndrome: marked improvement of renal function and reduction of proteinuria after therapy with human anti-interleukin-1β monoclonal antibody canakinumab.
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  • Description of a new family with cryopyrin-associated periodic syndrome: risk of visual loss in patients bearing the R260W mutation.
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  • Fever of unknown origin and leukemoid reaction as initial presentation of adult-onset Still's disease.
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  • Complete atrioventricular block and aseptic meningitis in a patient with adult-onset Still's disease and concurrent hemophagocytic syndrome.
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  • Refractory urticaria in adult-onset Still's disease.
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  • Diagnosis and classification of adult Still's disease.
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  • Late onset of Crohn’s disease in familial Mediterranean fever: the necessity of anti-TNF treatment.
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  • Protracted febrile myalgia in an afebrile child with familial Mediterranean fever.
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  • Are MEFV mutations susceptibility factors in enthesitis-related arthritis patients in the eastern Mediterranean?
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  • Evaluation of platelet indices in children with familial Mediterranean fever: confounding factors should be considered.
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  • Primary headaches in pediatric patients with chronic rheumatic disease.
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  • Coexistence of two rare genetic disorders: Kartagener syndrome and familial Mediterranean fever.
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  • Urticarial vasculitis and Schnitzler syndrome.
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  • Tocilizumab in Adult-onset Still's Disease: the Israeli Experience.
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  • Reactive haemophagocytic syndrome in a patient with adult-onset Still's disease: beta-lactams as trigger?
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  • A case of adult onset Still's disease with flare of arthritis.
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  • Updates on the risk markers and outcomes of severe juvenile idiopathic arthritis-associated uveitis.
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  • High complication rate in revision total hip arthroplasty in juvenile idiopathic arthritis.
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  • Quality of life measures and psychiatric symptoms in adolescents with systemic lupus erythematosus and familial Mediterranean fever1).
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Januar

  • Anakinra for cryopyrin-associated periodic syndrome.
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  • Critical role for inflammasome-independent IL-1β production in osteomyelitis.
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  • Inflammasome-independent IL-1β mediates autoinflammatory disease in Pstpip2-deficient mice.
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  • IL-1 Blockade in Autoinflammatory Syndromes.
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  • Diagnostic criteria of familial Mediterranean fever.
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  • MEFV gene mutations and cardiac phenotype in children with familial Mediterranean fever: a cohort study.
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  • Autoinflammatory diseases.
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  • Schnitzler syndrome.
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  • IL-1 Blockade in Autoinflammatory Syndromes.
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  • Diagnosis and classification of adult Still's disease.
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  • Canakinumab in a case of Adult onset Still's disease: Efficacy only on systemic manifestations.
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  • Cardiac magnetic resonance in myocarditis from adult onset Still's disease successfully treated with anakinra.
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  • Life-threatening complications of adult-onset Still's disease.
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  • Adult onset Still's disease with persistent skin lesions complicated by secondary hemophagocytic lymphohistiocytosis.
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  • Tocilizumab for the treatment of adult-onset Still's disease: results from a case series.
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  • Biologic treatments for adult-onset Still's disease.
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  • Systemic juvenile idiopathic arthritis-like syndrome in mice following stimulation of the immune system with complete Freund's adjuvant: Regulation by IFN- γ
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  • Immunological characteristics and T cell receptor clonal diversity in children with systemic juvenile idiopathic arthritis undergoing T cell depleted autologous stem cell transplantation.
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  • Juvenile chronic arthritis and the craniovertebral junction in the paediatric patient: review of the literature and management considerations.
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  • Effect of biologic treatments on growth in children with juvenile idiopathic arthritis.
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  • Advances in the pathogenesis and treatment of systemic juvenile idiopathic arthritis.
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  • Anxiety and depression in adult patients with familial Mediterranean fever: a study comparing patients living in Germany and Turkey.
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  • MEFV gene mutations and cardiac phenotype in children with familial Mediterranean fever: a cohort study.
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  • Decreased vitamin D levels in children with familial Mediterranean fever.
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  • Colchicine-free remission in familial Mediterranean fever: featuring a unique subset of the disease-a case control study.
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  • Assessing Disease Severity and Activity in Patients with Familial Mediterranean Fever.
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  • The frequency of Familial Mediterranean fever gene mutations and genotypes at Kirikkale and comparison with the mean of regional MEFV mutation frequency of Turkey.
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  • Coexistence of familial Mediterranean fever and rheumatoid arthritis.
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  • MEFV gene variations in patients with systemic lupus erythematosus.
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Aktuelles & Studien

4th Autoinflammation Masterclass 28. - 29.04.2016 in Berlin

11.04.2016  |  Kat: News

Dear Colleagues, It is a pleasure for us to cordially welcome you to the beautiful city of Berlin...

8th International Congress of Familial Mediterranean Fever and Systemic Autoinflammatory Diseases

30.09.2015  |  Kat: News

30. September - 03. Oktober 2015 in Dresden

Novel Concepts in Innate Immunity (NCII) 2015

24.03.2015  |  Kat: News

23. - 25. September 2015 in Tübingen.