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Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 5/2008, Volume 28, Issue S1, pp. 73 - 83
Autoinflammatory diseases are a group monogenic inflammatory conditions characterized by an early onset during childhood.Under the term “periodic fevers” are... 
tumor necrosis factor (TNF) receptor-associated syndrome | Medical Microbiology | Biomedicine | Immunology | Internal Medicine | Infectious Diseases | Familial Mediterranean fever | mevalonate kinase deficiency | cryopyrinopathies | Tumor necrosis factor (TNF) receptor-associated syndrome | Cryopyrinopathies | Mevalonate kinase deficiency | RECURRENT MULTIFOCAL OSTEOMYELITIS | TNF RECEPTOR | INTERLEUKIN-1 BLOCKADE | necrosis factor (TNF) receptor-associated syndrome | CLINICAL-FEATURES | IMMUNOLOGY | CONGENITAL DYSERYTHROPOIETIC ANEMIA | mevalonate kinase deficiency tumor | MEVALONATE KINASE | HYPERIMMUNOGLOBULINEMIA-D | PEDIATRIC GRANULOMATOUS ARTHRITIS | familial Mediterranean fever | PERIODIC FEVER | Autoimmune Diseases - physiopathology | Cytoskeletal Proteins - genetics | Mevalonate Kinase Deficiency - physiopathology | Humans | Child, Preschool | Infant | Mevalonate Kinase Deficiency - genetics | CARD Signaling Adaptor Proteins - genetics | Mevalonate Kinase Deficiency - therapy | Autoimmune Diseases - genetics | Adult | Amyloidosis - etiology | Steroids - therapeutic use | Child | CARD Signaling Adaptor Proteins - immunology | Autoimmune Diseases - complications | Familial Mediterranean Fever - genetics | Familial Mediterranean Fever - complications | Genotype | Familial Mediterranean Fever - therapy | Inflammation | Autoimmune Diseases - diagnosis | Mevalonate Kinase Deficiency - diagnosis | Pyrin | Familial Mediterranean Fever - physiopathology | Adaptor Proteins, Signal Transducing - genetics | Age of Onset | Mevalonate Kinase Deficiency - complications | Autoimmune Diseases - therapy | Familial Mediterranean Fever - diagnosis | Mutation | Care and treatment | Children | Diagnosis | Tumor necrosis factor | Diseases
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
The New England Journal of Medicine, ISSN 0028-4793, 05/2018, Volume 378, Issue 20, pp. 1908 - 1919
Journal Article
Journal Article
Medicine, ISSN 0025-7974, 2008, Volume 87, Issue 6, pp. 301 - 310
Journal Article
Medicine (United States), ISSN 0025-7974, 2016, Volume 95, Issue 11, p. e3027
Journal Article
Rheumatology, ISSN 1462-0324, 2016, Volume 55, Issue suppl 2, pp. ii23 - ii29
Autoinflammatory syndromes are disorders with an exaggerated inflammatory response, mostly in the absence of an appropriate trigger. Prototypic... 
Interleukin-1 | Autoinflammation | Cytokines | Periodic fever | Interleukin-1 receptor antagonist | Canakinumab | Anakinra | interleukin-1 | MEVALONATE KINASE-DEFICIENCY | PERIODIC FEVER SYNDROME | autoinflammation | MONONUCLEAR-CELLS | FOLLOW-UP | OPEN-LABEL | RHEUMATOLOGY | anakinra | canakinumab | FAMILIAL MEDITERRANEAN FEVER | HYPERIMMUNOGLOBULINEMIA-D | cytokines | QUALITY-OF-LIFE | SCHNITZLER-SYNDROME | periodic fever | HIDRADENITIS SUPPURATIVA | interleukin-1 receptor antagonist | Antibodies, Monoclonal, Humanized - therapeutic use | Mevalonate Kinase Deficiency - physiopathology | Colchicine - therapeutic use | Humans | Familial Mediterranean Fever - genetics | Hereditary Autoinflammatory Diseases - immunology | Interleukin-1beta - immunology | Antibodies, Monoclonal - therapeutic use | Phosphotransferases (Alcohol Group Acceptor) - genetics | Familial Mediterranean Fever - drug therapy | Familial Mediterranean Fever - immunology | Mevalonate Kinase Deficiency - drug therapy | Mevalonate Kinase Deficiency - genetics | Molecular Targeted Therapy | Hereditary Autoinflammatory Diseases - drug therapy | Tubulin Modulators - therapeutic use | Familial Mediterranean Fever - physiopathology | Interleukin 1 Receptor Antagonist Protein - therapeutic use | Mevalonate Kinase Deficiency - immunology | Hereditary Autoinflammatory Diseases - physiopathology | Antirheumatic Agents - therapeutic use | Hereditary Autoinflammatory Diseases - genetics
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