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Newsletter 2012

Dezember

Innate immune processes in lupus erythematosus.
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Phagocyte-derived S100 proteins in autoinflammation: Putative role in pathogenesis and usefulness as biomarkers.
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How not to miss autoinflammatory diseases masquerading as urticaria.
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The association of TNFRSF1A gene and MEFV gene mutations with adult onset Still's disease.
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Adult onset Still's disease: experience from a tertiary care rheumatology unit.
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Anakinra in adult onset still's disease: Long term treatment in patients resistant to conventional therapy.
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Efficacy and Safety of Biologic Treatments in Familial Mediterranean Fever.
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Regulation of interleukin 1α secretion by inflammasomes.
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Microarray-based gene expression profiling in patients with cryopyrin-associated periodic syndromes defines a disease-related signature and IL-1-responsive transcripts.
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The calcium-sensing receptor regulates the NLRP3 inflammasome through Ca2+ and cAMP.
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Strong induction of AIM2 expression in human epidermis in acute and chronic inflammatory skin conditions.
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Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiency.
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Schnitzler syndrome complicated by membranous nephropathy.
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Ocular manifestations of the autoinflammatory syndromes.
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Muckle-wells syndrome and male hypofertility: a case series.
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Inflammation: Rilonacept for familial Mediterranean fever?
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Factors Associated with Achievement of Inactive Disease in Children with Juvenile Idiopathic Arthritis Treated with Etanercept.
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November

Autoinflammation and autoimmunity: bridging the divide.
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An overview of interleukin-1 receptor antagonist, anakinra, in the treatment of cutaneous diseases.
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The calcium-sensing receptor regulates the NLRP3 inflammasome through Ca(2+) and cAMP.
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Biologic drugs in autoinflammatory syndromes.
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Targeting interleukin-1β in CAPS (cryopyrin-associated periodic) syndromes: what did we learn?
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Tumour necrosis factor receptor-associated periodic syndrome (TRAPS): state of the art and future perspectives.
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Reduced expression of NLRP3 and MEFV in human ischemic heart tissue.
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Familial Mediterranean Fever - An increasingly important childhood disease in Sweden.
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Association of Inflammatory Bowel Disease With Familial Mediterranean Fever In Turkish Children.
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The scintigraphic evaluation and genetic correlation of joint involvements in pediatric patients with familial Mediterranean fever.
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Exertional muscle pain in familial Mediterranean fever patients evaluated by MRI and (31)P magnetic resonance spectroscopy.
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Familial Mediterranean fever in Germany: clinical presentation and amyloidosis risk.
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Pregnancy outcome in women with familial Mediterranean fever.
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The diagnostic evaluation of patients with potential adult-onset autoinflammatory disorders: our experience and review of the literature.
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Two-year outcome of juvenile idiopathic arthritis in current daily practice: what can we tell our patients?
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Application of the Yamaguchi criteria for classification of "suspected" systemic juvenile idiopathic arthritis (sJIA).
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Consensus statement on blocking the effects of interleukin-6 and in particular by interleukin-6 receptor inhibition in rheumatoid arthritis and other inflammatory conditions.
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Efficacy of biological agents in juvenile idiopathic arthritis: a systematic review using indirect comparisons.
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Seeking insights into the EPidemiology, treatment and Outcome of Childhood Arthritis through a multinational collaborative effort: Introduction of the EPOCA study.
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CLARITY -- ChiLdhood Arthritis Risk factor Identification sTudY.
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Genome-scale case-control analysis of CD4+ T-cell DNA methylation in juvenile idiopathic arthritis reveals potential targets involved in disease.
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Blocking the effects of interleukin-6 in rheumatoid arthritis and other inflammatory rheumatic diseases: systematic literature review and meta-analysis informing a consensus statement.
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Towards a role of ultrasound in children with juvenile idiopathic arthritis.
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Foot function is well preserved in children and adolescents with juvenile idiopathic arthritis who are optimally managed.
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Pulmonary hypertension and other potentially fatal pulmonary complications in systemic juvenile idiopathic arthritis.
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Oktober

A novel mutation in the interleukin-1 receptor antagonist associated with intrauterine disease onset.
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Mean platelet volume and β-thromboglobulin levels in familial mediterranean fever: Effect of colchicine use?
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Juvenile spondyloarthropathies.
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The role of interleukin-1 in allergy-related disorders.
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Guidance on the use of canakinumab in patients with cryopyrin-associated periodic syndrome in Japan.
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Long-term efficacy and safety profile of rilonacept in the treatment of cryopryin-associated periodic syndromes: results of a 72-week open-label extension study.
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Autophagy contributes to inflammation in patients with TNFR-associated periodic syndrome (TRAPS).
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Efficacy of an Interleukin-1β Receptor Antagonist (Anakinra) in Idiopathic Recurrent Pericarditis.
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Activated phenotype of circulating neutrophils in familial Mediterranean fever.
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Rilonacept for colchicine-resistant or -intolerant familial mediterranean Fever: a randomized trial.
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Plasminogen activator inhibitor-1 gene polymorphism in Iranian Azeri Turkish patients with FMF disease and its association with amyloidosis.
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The M694V mutation in Armenian-Americans: a 10-year retrospective study of MEFV mutation testing for familial Mediterranean fever at UCLA.
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Familial mediterranean Fever in siblings.
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September

How not to miss autoinflammatory diseases masquerading as urticaria.
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Pattern recognition receptors in infectious skin diseases.
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Clinical spectrum of the pseudotumor cerebri in children: Etiological, clinical features, treatment and prognosis.
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Exertional leg pain as a manifestation of occult spondyloarthropathy in familial Mediterranean fever: an MRI evaluation.
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High Frequency of Inherited Variants in the MEFV Gene in Acute Lymphocytic Leukemia.
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Elevated interleukin-18 secretion from monoclonal IgM+ B cells in a patient with Schnitzler syndrome.
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Cutting edge: IL-6 is a marker of inflammation with no direct role in inflammasome-mediated mouse models.
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Inflammasomes and Their Roles in Health and Disease.
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Optical projection tomography reveals dynamics of HEV growth after immunization with protein plus CFA and features shared with HEVs in acute autoinflammatory lymphadenopathy.
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The dual roles of inflammatory cytokines and chemokines in the regulation of autoimmune diseases and their clinical implications.
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August

Adult Onset Still's Disease and Autoinflammation.
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Autoinflammation and autoimmunity: Bridging the divide.
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The impact of MEFV gene identification on familial Mediterranean fever: an appraisal after 15 years.
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A case of Takayasu's arteritis associated with familial Mediterranean fever.
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Apoptosis-associated speck-like protein containing a CARD (ASC) expression profiles in familial Mediterranean fever (FMF) patients with different MEFV mutation patterns.
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Ocular manifestations of the autoinflammatory syndromes.
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Analysis of Cytotoxic T Lymphocyte Antigen-4 (CTLA-4) Promoter -318C/T and +49A/G Gene Polymorphisms in Turkish Patients with Familial Mediterranean Fever.
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Late presentation of familial Mediterranean fever associated with P369S/R408Q variant in the MEFV gene.
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Misdiagnosis of familial Mediterranean fever in patients with Anderson-Fabry disease.
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Familial Mediterranean fever in Germany: epidemiological, clinical, and genetic characteristics of a pediatric population.
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An Atypical Familial Mediterranean Fever Patient Who Developed Ulcers in the Terminal Ileum and Recurrent Abscess-like Lesions in Multiple Organs.
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Recurrent pericarditis: Autoimmune or autoinflammatory?
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Incomplete response to colchicine in M694V homozygote FMF patients.
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Familial Mediterranean fever: New phenotypes.
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The diagnostic evaluation of patients with potential adult-onset autoinflammatory disorders: Our experience and review of the literature.
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Canakinumab in Schnitzler Syndrome.
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Serum leptin, resistin, visfatin and adiponectin levels in tumor necrosis factor receptor-associated periodic syndrome (TRAPS).
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Recurrent abdominal pain as the presentation of tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in an Asian girl: A case report and review of the literature.
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Tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in Japan: a review of the literature.
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The diagnostic evaluation of patients with potential adult-onset autoinflammatory disorders: Our experience and review of the literature.
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Pericardial syndromes: an update after the ESC guidelines 2004.
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Long-term clinical course of patients carrying the Q703K mutation in the NLRP3 gene: a case series.
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Ocular manifestations of the autoinflammatory syndromes.
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Cryopyrin-Associated Periodic Syndrome.
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Biologic drugs in autoinflammatory syndromes.
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Ocular manifestations of the autoinflammatory syndromes.
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Early-onset chronic inflammatory disease associated with maternal microchimerism.
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PSTPIP2 deficiency in mice causes osteopenia and increased differentiation of multipotent myeloid precursors into osteoclasts.
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Immunoregulation by naturally occurring and disease-associated autoantibodies : binding to cytokines and their role in regulation of T-cell responses.
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Blau syndrome, clinical and genetic aspects.
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Gout as autoinflammatory disease: New mechanisms for more appropriated treatment targets.
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Tumour necrosis factor receptor-associated periodic syndrome (TRAPS): State of the art and future perspectives.
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Biologic drugs in autoinflammatory syndromes.
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Systemic juvenile idiopathic arthritis.
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Autoinflammatory diseases: How to put the fire inside the body out?
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Autophagy in immunity: Implications in etiology of autoimmune/autoinflammatory diseases.
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Familial Mediterranean fever: New phenotypes.
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Periodic fevers with aphthous stomatitis, pharyngitis, and adenitis (PFAPA).
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New genetic interpretation of old diseases.
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Amyloidosis in autoinflammatory syndromes.
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Redox control of NLRP3 inflammasome activation in health and disease.
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Pericarditis: sometimes an autoinflammatory disease?
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Autoinflammatory syndromes: Fever is not always a sign of infection.
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Therapy refractory polyarthritis and fever
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Successful treatment of a patient with tumor necrosis factor receptor-associated periodic syndrome using a half-dose of etanercept.
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Infliximab therapy for familial Mediterranean fever-related amyloidosis: case series with long term follow-up.
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Chronic urticaria with monoclonal IgG gammopathy: a clinical variant of Schnitzler syndrome?
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Treating inflammation by blocking interleukin-1 in a broad spectrum of diseases.
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Juli

Naturally occurring genetic variants of human caspase-1 differ considerably in structure and the ability to activate interleukin-1β (IL-1β).
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Lighting the fires within: the cell biology of autoinflammatory diseases.
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Autoinflammation: translating mechanism to therapy.
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The factors considered as trigger for the attacks in patients with familial Mediterranean fever.
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Magnetic resonance imaging can detect thoracic inflammation due to familial Mediterranean fever.
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Progressive familial hearing loss in Muckle-Wells syndrome.
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Efficacy and safety of the interleukin-1 antagonist rilonacept in Schnitzler syndrome: an open-label study.
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Naturally occurring genetic variants of human caspase-1 differ considerably in structure and the ability to activate interleukin-1β (IL-1β).
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Critical role for mast cells in interleukin-1β-driven skin inflammation associated with an activating mutation in the nlrp3 protein.
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Juni

Adult-onset Still's disease and chronic recurrent multifocal osteomyelitis: a hitherto undescribed manifestation of autoinflammation.
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A rare cause of massive ascites: Familial Mediterranean fever.
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Is familial Mediterranean fever (FMF) common in patients with negative appendectomy?
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Colchicine is a Safe Drug in Children with Familial Mediterranean Fever.
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Does mean platelet volume influence the attack or attack-free period in the patients with Familial Mediterranean fever?
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The autoinflammatory diseases.
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Diffuse amyloid deposition in thyroid gland: a cause for concern in familial Mediterranean fever.
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Increased angiogenesis and enhanced bone formation in patients withIGM monoclonal gammopathy and urticarial skin rash: new insight intothe biology of the Schnitzler syndrome.
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Treatment of autoinflammatory diseases: results from the Eurofever Registry and a literature review.
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Deficient production of IL-1 receptor antagonist and IL-6 coupled to oxidative stress in cryopyrin-associated periodic syndrome monocytes.
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Autoinflammatory grey matter lesions in humans: cortical encephalitis, clinical disorders, experimental models.
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Mai

Interleukin-1, inflammasomes, autoinflammation and the skin.
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Gain-of-function Pyrin mutations induce NLRP3 protein-independent interleukin-1β activation and severe autoinflammation in mice.
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Diffuse pulmonary amyloidosis due to Familial Mediterranean Fever, a rare presentation.
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Frequency of alterations in the MEFV gene and clinical signs in familial Mediterranean fever in Central Anatolia, Turkey.
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Tumor Necrosis Factor-α Gene Polymorphisms in FMF and Their Association With Amyloidosis.
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Clinical impact of MEFV mutations in children with periodic fever in a prevalent western European Caucasian population.
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Familial Mediterranean fever: risk factors, causes of death, and prognosis in the colchicine era.
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Neonatal autoimmune diseases: a critical review.
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Clinical and histopathologic review of Schnitzler syndrome: The Mayo Clinic experience (1972-2011).
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Different clinical presentation of the hyperimmunoglobulin D syndrome (HIDS) (four cases from Turkey).
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April

Cryopyrin-associated periodic syndromes: diagnosis and management.
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März

Immunology in clinic review series; focus on autoinflammatory diseases: update on monogenic autoinflammatory diseases: the role of interleukin (IL)-1 and an emerging role for cytokines beyond IL-1.
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Februar

Diagnosis of PFAPA syndrome applied to a cohort of 17 adults with unexplained recurrent fevers.
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Dermal Interleukin-1 Expression and Effective and Long-lasting Therapy with Interleukin-1 Receptor Antagonist Anakinra in Schnitzler Syndrome.
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Familial Mediterranean fever-associated mutation pyrin E148Q as a potential risk factor for multiple sclerosis.
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Januar

Rare hereditary autoinflammatory disorders: Towards an understanding of critical in vivo inflammatory pathways.
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Different clinical presentation of the hyperimmunoglobulin D syndrome (HIDS) (four cases from Turkey).
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Aberrant expression of costimulatory molecules in splenocytes of the mevalonate kinase-deficient mouse model of human hyper-IgD syndrome (HIDS).
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Etanercept and anakinra can prolong febrile episodes in patients with hyperimmunoglobulin D and periodic fever syndrome.
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Familial Mediterranean fever and related periodic fever syndromes/autoinflammatory diseases.
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Nucleotide-binding oligomerization domain-like receptors and inflammasomes in the pathogenesis of non-microbial inflammation and diseases.
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Familial Mediterranean fever and related periodic fever syndromes/autoinflammatory diseases.
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The relative contribution of environmental and genetic factors to phenotypic variation in familial Mediterranean fever (FMF).
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