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Additional file 2: Table S1. of Effects of HLA-DRB1 alleles on susceptibility and clinical manifestations in Japanese patients with adult onset Stillâ s disease

open access: yes, 2017
HLA-DRB1 allele carrier frequency in the patients with AOSD and age-matched healthy controls (1:2). (PDF 57 kb)
Asano, Tomoyuki   +27 more
openaire   +1 more source

Additional file 3: Table S2. of Effects of HLA-DRB1 alleles on susceptibility and clinical manifestations in Japanese patients with adult onset Stillâ s disease

open access: yes, 2017
Conditional logistic regression analysis between the protective HLA alleles in AOSD. (PDF 43 kb)
Asano, Tomoyuki   +27 more
openaire   +1 more source

CHARACTERISTICS OF ADULT-ONSET STILL’S DISEASE IN THE 21ST CENTURY [PDF]

open access: yes, 2018
The review gives an update on adult-onset Still’s disease: on its causes, the specific features of its pathogenesis, diagnosis, clinical presentations (with identification of subtypes), and treatment with consideration for the nature of the course of the
V. V. Lebedeva, Yu. V. Muravyev
core   +1 more source

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

Additional file 1: of Comparative study of Interleukin-18 (IL-18) serum levels in adult onset Stillâ s disease (AOSD) and systemic onset juvenile idiopathic arthritis (sJIA) and its use as a biomarker for diagnosis and evaluation of disease activity

open access: yes, 2019
Table S1. List of main diganoses in adult control group. Table S2. List of diseases in childrenâ s control group. Table S3. Frequency of symptoms in active sJIA. (DOCX 21 kb)
Kudela, Holger   +4 more
openaire   +1 more source

Case report Adult-onset Still’s disease as a mask of Hodgkin lymphoma

open access: yes, 2015
Adult-onset Still’s disease is a rare disorder, which creates difficulties in making a proper diagnosis. Ambiguous symptoms and results of auxiliary tests, lack of unequivocal diagnostic tests and the need to exclude other causes of the disease are major
Katarzyna Pawlak-Buś   +2 more
core   +1 more source

The diagnostic challenge of Adult-onset Still’s disease [PDF]

open access: yes, 2018
Adult-onset Still’s disease (AOSD) is a rare systemic inflammatory disease of unknown etiology, characterized by symptoms including high fever, salmon-pink rash, and also inflammatory symptoms such as sore throat, arthritis or arthralgia and ...
Rostamipour, H.A., Rastegarian, L
core   +1 more source

Adult-onset Still’s disease with prominent polyserositis

open access: yes, 2018
Adult-onset Still’s disease is a systemic autoinflammatory disease the presentation of which can often mimic infection. As a consequence, there is often a delay in diagnosis.
Ali Sibtain Farooq Sheikh   +2 more
core   +1 more source

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

ADULT-ONSET STILL'S DISEASE TODAY

open access: yesНаучно-практическая ревматология, 2017
The lecture gives an update on adult-onset Still's disease, including that on the specific features of the clinical picture and treatment of this disease.
Yu. V. Muravyev, V. V. Lebedeva
doaj   +1 more source

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