Results 21 to 30 of about 4,345 (272)

The association between adult-onset Still’s disease and collapsing glomerulopathy: a case report

open access: yesJournal of Medical Case Reports, 2022
Background Collapsing glomerulopathy, characterized by marked hypertrophy and hyperplasia of the podocytes with eventual collapse of the glomerular tuft, is an important cause of end-stage renal disease. Among the many causes of collapsing glomerulopathy,
Matas Orentas   +3 more
doaj   +1 more source

Therapy with canakinumab for adult-onset still's disease

open access: yesНаучно-практическая ревматология, 2019
Still's disease in children (systemic-onset juvenile idiopathic arthritis, SoJIA) and in adults (adult-onset Still's disease) are considered as non-familial systemic autoinflammatory diseases of unknown etiology driven by similar immunopathogenetic ...
E. L. Nasonov
doaj   +1 more source

Treatment of adult-onset Still's disease: a review [PDF]

open access: yes, 2014
Adult-onset Still's disease (AOSD) is a rare inflammatory disorder that has been recently classified as a polygenic autoinflammatory disorder. The former classification, based on the disease course, seems to be quite dated.
Gerfaud-Valentin, M.   +3 more
core   +3 more sources

A promoter haplotype of the interleukin-18 gene is associated with juvenile idiopathic arthritis in the Japanese population [PDF]

open access: yes, 2015
journal ...
HARA, Masako   +8 more
core   +2 more sources

Adult-onset Still's disease

open access: yesAutoimmunity 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   +5 more sources

Adult-onset Still's disease with atypical cutaneous manifestations [PDF]

open access: yes, 2018
The diagnosis of adult-onset Still's disease (AOSD) can be very difficult. There are no specific tests available, and diagnosis is usually based on a symptom complex and the well-described typical evanescent rash seen in the majority of patients. However,
Juarez, Pablo   +6 more
core   +1 more source

Pregnancy-Associated Onset of Adult-Onset Still's Disease [PDF]

open access: yesAmerican Journal of Perinatology Reports
Nawras Zayat   +8 more
doaj   +2 more sources

Development and Role in Therapy of Canakinumab in Adult-Onset Still's Disease [PDF]

open access: yes, 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

Elevated Troponin Serum Levels in Adult Onset Still's Disease [PDF]

open access: yes, 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

Adult-onset Still's Disease: A Case Report

open access: yesJournal 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

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