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Journal of Rheumatology, ISSN 0315-162X, 11/2018, Volume 45, Issue 11, pp. 1605 - 1607
The SAPHO syndrome is a group of disorders that manifest as synovitis, acne, pustulosis, hyperostosis, and osteitis. Of these, acne damage can present as acne... 
PYODERMA-GANGRENOSUM | RHEUMATOLOGY | ACNE | AUTOINFLAMMATION
Journal Article
Aktuelle Rheumatologie, ISSN 0341-051X, 2019, Volume 44, Issue 3, pp. 186 - 198
Journal Article
Nauchno-Prakticheskaya Revmatologiya, ISSN 1995-4484, 2018, Volume 56, Issue 2, pp. 253 - 256
Journal Article
Rheumatology, ISSN 1462-0324, 10/2019, Volume 58, Issue 10, pp. 1818 - 1821
Abstract Objective To define the characteristics of children expressing the FMF phenotype under colchicine until it was ceased and to compare the clinical... 
GENE | children | MUTATION | DISEASE | autoinflammation | colchicine | familial Mediterranean fever | RHEUMATOLOGY
Journal Article
European journal of immunology, ISSN 0014-2980, 5/2016, Volume 46, Issue 5, pp. 1067 - 1081
IL-37 is unique in the IL-1 family in that unlike other members of the family, IL-37 broadly suppresses innate immunity. IL-37 can be elevated in humans with... 
Autoinflammation | Toll Receptors | IL-1 Family | Caspase-1
Journal Article
Journal of immunology (Baltimore, Md. : 1950), ISSN 0022-1767, 9/2018, Volume 201, Issue 6, pp. 1639 - 1644
Mice homozygous for the Tyr208Asn amino acid substitution in the carboxy terminus of SHP-1 (referred to as Ptpn6 spin mice) spontaneously develop a severe... 
neutrophilic dermatosis | CARD9 | autoinflammation | macrophage | SHP-1 | IL-1α | neutrophils
Journal Article
Ocular Immunology and Inflammation, ISSN 0927-3948, 2018, pp. 1 - 9
To present the ocular findings of the members of a family that has the diagnosis of Muckle Wells syndrome, a form of cryopyrin associated periodic syndrome... 
cryoprin | Muckle Wells syndrome | Autoinflammation | conjunctivitis | uveitis
Journal Article
Sovremennaâ Revmatologiâ, ISSN 1996-7012, 04/2017, Volume 11, Issue 2, pp. 41 - 46
Autoinflammatory diseases (AIDs) are a group of rare disorders characterized by persistent or recurrent inflammation caused by the hyperactivation of mediators... 
autoinflammation | NLRP12 | inflammasome
Journal Article
Frontiers in Immunology, ISSN 1664-3224, 11/2019, Volume 10
Type I interferonopathies cover a phenotypically heterogeneous group of rare genetic diseases including the recently described proteasome-associated... 
ER stress | autoinflammation | proteasome | unfolded protein response | TCF11/Nrf1 | mTORC1
Journal Article
ALLERGOLOGIE, ISSN 0344-5062, 07/2019, Volume 42, Issue 7, pp. 301 - 304
We report on a 52-year-old patient who presented with longstanding chronic urticanal rash refractory under oral antihistamines and omalizumab. She also... 
ALLERGY | urticaria | autoinflammation | STING | THEM173 gene
Journal Article
Arthritis and Rheumatology, ISSN 2326-5191, 03/2016, Volume 68, Issue 3, pp. 557 - 560
Journal Article
Journal of Leukocyte Biology, ISSN 0741-5400, 07/2019, Volume 106, Issue 1, pp. 171 - 185
Various intracellular pattern recognition receptors (PRRs) recognize cytosolic pathogen‐associated molecular patterns (PAMPs) and damage‐associated molecular... 
cGAMP | autoimmunity | inflammation | cGAS | autoinflammation | STING | type 1 IFNs | CYCLIC GMP-AMP | SYSTEMIC-LUPUS-ERYTHEMATOSUS | KAPPA-B ACTIVATION | CYTOSOLIC DNA SENSOR | IMMUNOLOGY | INTERFERON-MEDIATED AUTOINFLAMMATION | MITOCHONDRIAL-DNA | CELL-DEATH | CELL BIOLOGY | NEUTROPHIL EXTRACELLULAR TRAPS | INNATE IMMUNE SENSOR | HEMATOLOGY | PATTERN-RECOGNITION RECEPTORS
Journal Article
Current Opinion in Allergy and Clinical Immunology, ISSN 1528-4050, 12/2017, Volume 17, Issue 6, pp. 398 - 404
Journal Article