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Hautarzt, ISSN 0017-8470, 2019
Schnitzler syndrome is a very rare acquired systemic disease with many similarities to hereditary autoinflammatory syndromes. The main characteristics are... 
Urticarial rash | Hereditary autoinflammatory syndrome | Interleukin-1 | Anakinra | Systemic disease
Journal Article
Zeitschrift fur Rheumatologie, ISSN 0340-1855, 02/2019, Volume 78, Issue 1, pp. 43 - 54
Journal Article
ZEITSCHRIFT FUR RHEUMATOLOGIE, ISSN 0340-1855, 02/2019, Volume 78, Issue 1, pp. 43 - 54
Schnitzler syndrome is avery rare acquired systemic disease with many similarities to hereditary autoinflammatory syndromes. The main characteristics are... 
Urticarial rash | CELLS | Interleukin-1 | DIFFERENTIAL-DIAGNOSIS | EFFICACY | SAFETY | INTERLEUKIN-1-BETA | CANAKINUMAB | Hereditary autoinflammatory syndrome | RHEUMATOLOGY | PATHOPHYSIOLOGY | NEUTROPHILIC URTICARIAL DERMATOSIS | Systemic disease | Anakinra | REMISSION
Journal Article
Hautarzt, ISSN 0017-8470, 09/2018, Volume 69, Issue 9, pp. 761 - 772
Journal Article
Nature Genetics, ISSN 1061-4036, 11/2001, Volume 29, Issue 3, pp. 301 - 305
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 08/2014, Volume 371, Issue 6, pp. 507 - 518
The stimulator of interferon genes (STING) protein bridges sensors of cytosolic DNA and the inflammatory pathway mediated by interferon-β. Activating mutations... 
MEDICINE, GENERAL & INTERNAL | FAMILIAL CHILBLAIN LUPUS | CYCLIC GMP-AMP | DNA | PROTEASOME SUBUNIT | LIPODYSTROPHY | SENSOR | MONOGENIC AUTOINFLAMMATORY DISEASES | EXPRESSION | I INTERFERON | INBORN-ERRORS | Up-Regulation | Phosphorylation | Humans | Infant | Male | Interferon-gamma - metabolism | Inflammation - metabolism | STAT1 Transcription Factor - metabolism | Skin Diseases, Vascular - genetics | Genes, Dominant | Female | Transcription, Genetic | Interferon-gamma - genetics | Cytokines - genetics | Infant, Newborn | Fibroblasts - metabolism | Skin Diseases, Vascular - metabolism | Cytokines - metabolism | Membrane Proteins - genetics | Sequence Analysis, DNA | Syndrome | Janus Kinases - antagonists & inhibitors | Lung Diseases - genetics | Pedigree | Age of Onset | Inflammation - genetics | Mutation | Pulmonary manifestations of general diseases | Blood circulation disorders | Genetic aspects | Research | Gene mutations | Risk factors | Transcription | Genes | Guanosine | Leukocytes (mononuclear) | Arthritis | Interleukin 6 | Cell activation | Vascular diseases | Lymphocytes | Cyclic GMP | Interleukin 1 | Peripheral blood | Fingers & toes | Fibroblasts | Janus kinase | Skin diseases | Children | Stat1 protein | Age | Deoxyribonucleic acid--DNA | Phenotypes | AMP | Patients | Endothelial cells | Studies | Biopsy | Ligands | Interferon | Autoimmune diseases | Apoptosis
Journal Article
HAUTARZT, ISSN 0017-8470, 09/2018, Volume 69, Issue 9, pp. 761 - 772
Journal Article
JOURNAL OF INFLAMMATION RESEARCH, ISSN 1178-7031, 2019, Volume 12, pp. 259 - 265
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2010, Volume 5, Issue 1, pp. 38 - 38
Journal Article
Arthritis Care & Research, ISSN 2151-464X, 04/2017, Volume 69, Issue 4, pp. 578 - 586
Objective Periodic fever syndrome (PFS) conditions are characterized by recurrent attacks of fever and localized inflammation. This study examined the... 
AUTOINFLAMMATORY DISEASES | MANAGEMENT | RHEUMATOLOGY | COLCHICINE-RESISTANT | RECOMMENDATIONS | FREQUENCY | Predictive Value of Tests | United States - epidemiology | Mevalonate Kinase Deficiency - epidemiology | Humans | Middle Aged | Child, Preschool | Infant | Male | Fever - epidemiology | Mevalonate Kinase Deficiency - genetics | Young Adult | Time Factors | Delayed Diagnosis - trends | Adult | Female | Familial Mediterranean Fever - epidemiology | Retrospective Studies | Child | Antirheumatic Agents - therapeutic use | Biological Products - therapeutic use | Severity of Illness Index | Familial Mediterranean Fever - genetics | Europe - epidemiology | Fever - diagnosis | Treatment Outcome | Familial Mediterranean Fever - drug therapy | Hereditary Autoinflammatory Diseases - diagnosis | Mevalonate Kinase Deficiency - drug therapy | Hereditary Autoinflammatory Diseases - drug therapy | Mevalonate Kinase Deficiency - diagnosis | Practice Patterns, Physicians' - trends | Rheumatology - trends | Adolescent | Fever - genetics | Aged | Familial Mediterranean Fever - diagnosis | Referral and Consultation - trends | Hereditary Autoinflammatory Diseases - epidemiology | Electronic Health Records | Fever - drug therapy | Hereditary Autoinflammatory Diseases - genetics | Mevalonate kinase | Mevalonic acid | Serositis | Tumor necrosis factor | Interleukin 1 receptor antagonist | Interleukin 1 | Tumor necrosis factor-TNF | Familial Mediterranean fever | Colchicine | Fever
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 07/2017, Volume 76, Issue 7, pp. 1191 - 1198
ObjectivesInflammasomes are multiprotein complexes that sense pathogens and trigger biological mechanisms to control infection. Nucleotide-binding... 
Arthritis | Inflammation | Fever Syndromes | Juvenile Idiopathic Arthritis | CELLS | SYSTEMIC-LUPUS-ERYTHEMATOSUS | DISEASES | SUBPOPULATIONS | FAMILIAL MEDITERRANEAN FEVER | JUVENILE IDIOPATHIC ARTHRITIS | MECHANISMS | INFLAMMASOMES | RHEUMATOLOGY | PYRIN | BLOOD | Interleukin-18 - immunology | Skin Diseases - genetics | Humans | Male | Precursor Cells, B-Lymphoid - immunology | Caspase 1 - immunology | Autoimmune Diseases - genetics | Netherlands | Apoptosis Regulatory Proteins - genetics | Female | Algeria | Child | Autoimmune Diseases - complications | Autoimmune Diseases - immunology | Hereditary Autoinflammatory Diseases - immunology | European Continental Ancestry Group | Skin Diseases - immunology | Arthritis, Juvenile - genetics | Syndrome | Hereditary Autoinflammatory Diseases - complications | Homozygote | Skin Diseases - complications | B-Lymphocytes - immunology | Arthritis, Juvenile - immunology | Adaptor Proteins, Signal Transducing - genetics | Adolescent | Arthritis, Juvenile - complications | Consanguinity | Mutation | African Continental Ancestry Group | Hereditary Autoinflammatory Diseases - genetics | Research | Gene mutations | Autoimmune diseases | NLRP proteins | Dyskeratosis | Pathogens | Cytokines | Transcription | Caspase | Patients | Inflammatory diseases | Caspase-1 | Interleukin 18 | Proteins | Vitiligo | Pyrin protein | Lymphocytes B | Rheumatoid arthritis | Gene mapping | Age | Immune system | Life Sciences | Human health and pathology | Rhumatology and musculoskeletal system
Journal Article
Journal Article