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dc.contributor.authorUlusoy H.
dc.contributor.authorBilgici A.
dc.contributor.authorKuru Ö.
dc.date.accessioned2020-06-21T09:23:58Z
dc.date.available2020-06-21T09:23:58Z
dc.date.issued2004
dc.identifier.issn1300-0691
dc.identifier.urihttps://hdl.handle.net/20.500.12712/3709
dc.description.abstractStill's disease is a systemic rheumatic disease of childhood which may persist into adulthood or may occur de novo in the adult population. It is classically distinguished by high fever, rash, arthritis, sore throat. Other clinical features may include lymphadenopathy, hepatosplenomegaly, pleuritis and pericarditis. Because there are no pathognomonic tests, patients frequently undergo a protracted investigative period. Serum ferritin levels greather than 5 folds of normal and glycosylated ferritin fraction lower than 20% of total ferritin are very specific for this disease. Up to one-third of patients is refractory to standard therapies, including methotrexate. Currently, blockade of tumor necrosis factor promises in the treatment of the disease.en_US
dc.language.isoturen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAdult Still's diseaseen_US
dc.subjectClinic featuresen_US
dc.subjectEtiologyen_US
dc.subjectTherapyen_US
dc.titleAdult Still's diseaseen_US
dc.title.alternativeEri?şki?n sti?ll hastaliğien_US
dc.typereviewen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume15en_US
dc.identifier.issue3en_US
dc.identifier.startpage203en_US
dc.identifier.endpage210en_US
dc.relation.journalJournal of Rheumatology and Medical Rehabilitationen_US
dc.relation.publicationcategoryDiğeren_US


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