Results 31 to 40 of about 4,997 (303)

Germinal center kinase-like kinase (GLK/MAP4K3) expression is increased in adult-onset Still's disease and may act as an activity marker

open access: yesBMC Medicine, 2012
Background Germinal center kinase-like kinase (GLK, also termed MAP4K3), a member of the MAP4K family, may regulate gene transcription, apoptosis and immune inflammation in response to extracellular signals.
Chen Der-Yuan   +6 more
doaj   +1 more source

Is exogenous administration of IL-1ra (anakinra) likely to induce severe depression? [PDF]

open access: yes, 2010
International ...
Aspe, Gilles   +4 more
core   +3 more sources

Adult Onset Still's Disease and Rocky Mountain Spotted Fever

open access: yesCase Reports in Medicine, 2010
Adult Still's Disease was first described in 1971 by Bywaters in fourteen adult female patients who presented with symptoms indistinguishable from that of classic childhood Still's Disease (Bywaters, 1971).
Paul Persad   +2 more
doaj   +1 more source

Association Between Peripheral Eosinophilia and Clinical Characteristics of Adult-onset Still’s Disease with Persistent Eruption: A Retrospective Study

open access: yesActa Dermato-Venereologica, 2021
Persistent eruption occurs in a subset of patients with adult-onset Still’s disease. In our experience, a considerable proportion of these patients present with peripheral eosinophilia.
Jia-Wei Liu   +6 more
doaj   +1 more source

Macrophage Activation Syndrome [PDF]

open access: yes, 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   +2 more
core   +2 more sources

ADULT-ONSET STILL’S DISEASE: ASPECTS OF THE HEMATOLOGY CLINIC

open access: yesСибирский научный медицинский журнал, 2019
The analysis of literature data on modern approaches in the diagnosis and treatment of adult-onset Still’s disease has been performed. A clinical case of Still’s disease associated with lymphadenopathy syndrome was demonstrated.
M. M. Agakishiev   +6 more
doaj   +1 more source

Cutaneous manifestations and histologic findings in the hyperimmunoglobulinemia D syndrome [PDF]

open access: yes, 1994
Contains fulltext : 4767.pdf (publisher's version ) (Open ...
Boom, B.W.   +3 more
core   +2 more sources

Pneumonitis in Adult Onset Still’s Disease: Uncommon or Under Diagnosed?

open access: yesActa Médica Portuguesa, 2017
The adult onset Still’s Disease is an uncommon entity characterized by multiple clinical manifestations. Pneumonitis, less often considered, deserves particular emphasis given the need for differential diagnosis and because it can progress to severe ...
Silvia Fernandes   +3 more
doaj   +1 more source

Adult-Onset Still’s Disease Presenting as Macrophage-Activation Syndrome With Critical Illness in the Third Trimester of Pregnancy: A Case Report

open access: yesCritical Care Explorations, 2021
BACKGROUND:. We report a case of a young woman with adult-onset Still’s disease presenting as macrophage-activation syndrome complicated by shock and respiratory failure during the third trimester of pregnancy. CASE SUMMARY:. A previously healthy 26-year-
Andrew T. Peters, MD   +1 more
doaj   +1 more source

Association between adult-onset still’s disease and COVID-19: A report of two cases and brief review

open access: yesSAGE Open Medical Case Reports
Adult-onset still’s disease is a rare multisystemic autoinflammatory disorder with an estimated annual incidence of 0.16–0.62 per 100,000 individuals worldwide. It is typically considered a diagnosis of exclusion.
Sarah Fet-He   +2 more
doaj   +1 more source

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