A comprehensive review on adult onset Still's disease

R Giacomelli, P Ruscitti, Y Shoenfeld - Journal of autoimmunity, 2018 - Elsevier
Adult-onset Still's disease (AOSD) is a systemic inflammatory disorder of unknown etiology
usually affecting young adults; spiking fever, arthritis and evanescent rash are commonly …

[HTML][HTML] Adult-onset Still's disease in focus: Clinical manifestations, diagnosis, treatment, and unmet needs in the era of targeted therapies

P Efthimiou, A Kontzias, P Hur, K Rodha… - Seminars in arthritis and …, 2021 - Elsevier
Abstract Background Adult-onset Still's disease (AOSD) is a rare systemic inflammatory
disorder of unknown etiology, characterized by a clinical triad of high spiking fever …

[HTML][HTML] Adult-onset Still's disease: evaluation of prognostic tools and validation of the systemic score by analysis of 100 cases from three centers

P Ruscitti, P Cipriani, F Masedu, D Iacono, F Ciccia… - BMC medicine, 2016 - Springer
Abstract Background Adult-onset Still's disease (AOSD) is rare inflammatory disease of
unknown etiology that usually affects young adults. The more common clinical …

Anakinra in children and adults with Still's disease

SJ Vastert, Y Jamilloux, P Quartier, S Ohlman… - …, 2019 - academic.oup.com
Systemic juvenile idiopathic arthritis and adult-onset Still's disease are rare
autoinflammatory disorders with common features, supporting the recognition of these being …

[HTML][HTML] Adult-onset Still's disease: clinical aspects and therapeutic approach

S Tomaras, CC Goetzke, T Kallinich, E Feist - Journal of clinical medicine, 2021 - mdpi.com
Adult-onset Still's disease (AoSD) is a rare systemic autoinflammatory disease characterized
by arthritis, spiking fever, skin rash and elevated ferritin levels. The reason behind the …

Expert consensus on the treatment of patients with adult-onset still's disease with the goal of achieving an early and long-term remission

R Giacomelli, R Caporali, F Ciccia… - Autoimmunity …, 2023 - Elsevier
We performed a comprehensive systematic targeted literature review and used the Delphi
method to formulate expert consensus statements to guide the treatment of adult-onset Still's …

Systemic autoinflammatory disease in adults

A Betrains, F Staels, R Schrijvers, I Meyts… - Autoimmunity …, 2021 - Elsevier
Systemic autoinflammatory disorders comprise an expanding group of rare conditions. They
are mediated by dysfunction of the innate immune system and share a core of phenotypic …

[HTML][HTML] Response to interleukin-1 inhibitors in 140 Italian patients with adult-onset Still's disease: a multicentre retrospective observational study

S Colafrancesco, R Priori, G Valesini… - Frontiers in …, 2017 - frontiersin.org
Background: Interleukin (IL)-1 plays a crucial role in the pathogenesis of Adult onset Still's
disease (AOSD). Objectives: To evaluate the efficacy and safety of anakinra (ANA) and …

Current and emerging biological therapy in adult-onset Still's disease

Y Ma, J Meng, J Jia, M Wang, J Teng, D Zhu… - …, 2021 - academic.oup.com
Adult-onset Still's disease (AOSD) is a rare, but characteristic non-familial, multi-genic
systemic auto-inflammatory disorder, characterized by high spiking fever, salmon-like …

Macrophage activation syndrome in patients affected by adult-onset Still disease: analysis of survival rates and predictive factors in the Gruppo Italiano di Ricerca in …

P Ruscitti, D Iacono, F Ciccia, G Emmi… - The Journal of …, 2018 - jrheum.org
Macrophage Activation Syndrome in Patients Affected by Adult-onset Still Disease: Analysis of
Survival Rates and Predictive Factors in the Gruppo Italiano di Ricerca in Reumatologia …