Results 21 to 30 of about 4,997 (303)
Elevated Troponin Serum Levels in Adult Onset Still's Disease [PDF]
, 2015 Adult onset Still's disease (AOSD) is a rare inflammatory systemic disease that occasionally may affect myocardium. Diagnosis is based on typical AOSD symptoms after the exclusion of well-known infectious, neoplastic, or autoimmune/autoinflammatory ...
Brugioni, Lucio +7 more
core +3 more sources
Suppurative necrotizing granulomatous lymphadenitis in adult-onset Still’s disease: a case report
Journal of Medical Case Reports, 2012 Introduction Lymphadenopathy is found in about 65% of patients with adult-onset Still’s disease and is histologically characterized by an intense, paracortical immunoblastic hyperplasia. Adult-onset Still’s disease has not been previously described as an
Assimakopoulos Stelios F +5 more
doaj +1 more source
Soluble interleukin-18 receptor complex is a novel biomarker in rheumatoid arthritis [PDF]
, 2011 Introduction There has been no report in the literature of a soluble form of interleukin (IL)-18 receptor α (IL-18Rα). In this study, we evaluated the levels and characteristics of soluble IL-18Rα (sIL-18Rα) in the sera of patients with ...
Satoko Takei +12 more
core +1 more source
Adult-onset Still's Disease: A Case Report
Journal of Nepal Medical Association, 2020 Adult-onset Still’s Disease is a rare auto inflammatory disorder of unknown etiology characterized mainly by high spiking fever, arthritis, evanescent rash and lymphadenopathy.
Ashok Sapkota +4 more
doaj +1 more source
Development and Role in Therapy of Canakinumab in Adult-Onset Still's Disease [PDF]
, 2018 Adult-onset Still's disease (AOSD) is a rare inflammatory disease of unknown etiology typically characterized by episodes of spiking fever, evanescent rash, arthralgia, leukocytosis, and hyperferritinemia. The pivotal role of interleukin (IL)-1 and other
Baggio, Chiara +4 more
core +1 more source
A case of adult‐onset Still's disease in a patient after a car accident
Clinical Case Reports, 2023 Key Clinical Message Adult‐onset Still's disease is a rare inflammatory condition with diverse clinical features. Yamaguchi criteria aid diagnosis, and pleural effusion and elevated ferritin levels are important markers.
Feride Yaman, Ali Kimiaei
doaj +1 more source
Rheumatoid arthritis is getting less frequent—results of a nationwide population-based cohort study [PDF]
, 2016 Objectives: The objectives of this study were to examine changes in incidence and prevalence of RA between 1990 and 2014, and to explore if there is any geographic variation in incidence and prevalence of RA in the UK Methods: Design Prospective ...
Abhishek Abhishek +17 more
core +3 more sources
Autoimmunity Reviews, 2014 First described in 1971, adult-onset Still's disease (AOSD) is a rare multisystemic disorder considered as a complex (multigenic) autoinflammatory syndrome. A genetic background would confer susceptibility to the development of autoinflammatory reactions to environmental triggers.
Gerfaud-Valentin, Mathieu +3 more
openaire +4 more sources
An interferon-inducible neutrophil-driven blood transcriptional signature in human tuberculosis [PDF]
, 2010 Tuberculosis (TB), caused by infection with Mycobacterium tuberculosis (M. tuberculosis), is a major cause of morbidity and mortality worldwide and efforts to control TB are hampered by difficulties with diagnosis, prevention and treatment 1,2.
A Falk +49 more
core +1 more source