Results 51 to 60 of about 5,213 (158)

Malaltia de Still de l'adult, revisió de 41 casos [PDF]

, 2012
Es descriuen les manifestacions clíniques, radiològiques, pronòstic i tractament de 41 pacients amb malaltia de Still de l'adult provinents de dos hospitals universitaris de Barcelona. La presentació clínica més freqüent va ser la poliartritis febril. El
Riera i Alonso, Elena, Universitat Autònoma de Barcelona. Departament de Medicina, Universitat Autònoma de Barcelona. Facultat de Medicina   +2 more
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Macrophage Activation Syndrome [PDF]

, 2015
Macrophage activation syndrome (MAS) is a potentially life-threatening complication of rheumatic diseases such as systemic juvenile idiopathic arthritis (sJIA) and systemic lupus erythematosus.
Clarke, Sarah L N, Ramanan, Athimalaipet V, Sen, Ethan S   +2 more
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Adult-Onset Still's Disease: A Review

Proceedings of Singapore Healthcare, 2013
Adult-onset Still's disease (AOSD) is an uncommon inflammatory condition characterised by high fever, leukocytosis with neutrophilia, arthralgia and skin rash.
Weng Seng Fong MBBS (Singapore), MRCP (UK), Nai Lee Lui MBBS (Singapore), MRCP (UK) M.Med (Int. Med) Singapore   +1 more
doaj   +1 more source

Socioeconomic costs and health-related quality of life in juvenile idiopathic arthritis: a cost-of-illness study in the United Kingdom [PDF]

, 2016
Background Juvenile idiopathic arthritis (JIA) refers to a number of rare chronic inflammatory diseases. Although JIA imposes a significant societal burden, limited data are available on the cost of JIA.

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Response letter to “Latent class analysis of 216 patients with adult-onset Still’s disease” by Sugiyama et al.

Arthritis Research & Therapy, 2022
Sugiyama et al. recently described in “Latent class analysis of 216 patients with adult-onset Still’s disease,” baseline characteristics, laboratory tests, treatment, relapse, and death of adult-onset Still’s disease (AOSD) patients from a Japanese ...
Marion Delplanque, Arsène Mekinian, Sophie Georgin-Lavialle   +2 more
doaj   +1 more source

RNA recognition by human TLR8 can lead to autoimmune inflammation. [PDF]

, 2013
Studies on the role of the RNA receptor TLR8 in inflammation have been limited by its different function in human versus rodents. We have generated multiple lines of transgenic mice expressing different levels of human TLR8. The high copy number chimeras
Ablasser, Alma-Martina Cepika, Barbalat, Barrat, Berry, Campbell, Cassidy, Chad Crain, Christensen, Claudio Tripodo, Cristiana Guiducci, Deane, Demaria, Döring, Ewald, Finkelberg, Forsbach, Franck J. Barrat, Fukui, Ganguly, Gantier, Gorden, Guiducci, Guiducci, Hattermann, Heil, Hemmi, Janke, John J. Cush, Lan, Liu, Lynda Bennett, Maschalidi, Mei Gong, Mellins, Mouchess, Nickerson, Pascual, Pierre Quartier, Pisitkun, Prinz, Quartier, Robert L. Coffman, Sacre, Sarvestani, Sparwasser, Subramanian, Virginia Pascual, Vollmer, Walsh, Wang, Zandieh, Zhaohui Xu   +52 more
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The progression of initial symptoms and its relationship with the clinical course in adult-onset Still’s disease: from the KEIO-AOSD cohort

EULAR Rheumatology Open
: Objectives: Adult-onset Still’s disease presents with nonspecific and heterogeneous features. This study aims to elucidate the development of initial symptoms and their relationship with the disease course in adult-onset Still’s disease.
Hiroya Tamai, Jun Kikuchi, Tsutomu Takeuchi, Yuko Kaneko   +3 more
doaj   +1 more source

Macrophage Activation Syndrome Associated with Adult-Onset Still’s Disease Successfully Treated with Anakinra

Case Reports in Rheumatology, 2016
Macrophage activation syndrome (MAS) is a potentially fatal complication of Adult-Onset Still’s disease (Still’s disease). Whereas an increasing body of evidence supports interleukin-1 (IL-1) blockade as a promising treatment for Still’s disease, whether
Aswini Kumar, Hiroshi Kato
doaj   +1 more source

Interleukin-18 as a diagnostic marker of adult-onset Still’s disease in older patients: a case report and review of the literature

Journal of Medical Case Reports, 2018
Background Adult onset Still’s disease is a systemic auto-inflammatory condition of unknown etiology characterized by intermittent spiking high fever, an evanescent salmon-pink or erythematous maculopapular skin rash, arthralgia or arthritis, and ...
Daisuke Usuda, Yoshiki Furumura, Kento Takeshima, Ryusho Sangen, Yasuhiro Kawai, Yuji Kasamaki, Yoshitsugu Iinuma, Tsugiyasu Kanda   +7 more
doaj   +1 more source

Defective iron supply for erythropoiesis and adequate endogenous erythropoietin production in the anemia associated with systemic-onset juvenile chronic arthritis. [PDF]

, 1996
peer reviewedSystemic-onset juvenile chronic arthritis (SoJCA) is associated with high levels of circulating interleukin-6 (IL-6) and is frequently complicated by severe microcytic anemia whose pathogenesis is unclear.
Barosi, G., Beguin, Yves, Cazzola, M., de Benedetti, F., Invernizzi, R., Martini, A., Ponchio, L., Ravelli, A., Rosti, V.   +8 more
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