Results 31 to 40 of about 6,693,207 (250)
BMC 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
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Case report Adult-onset Still’s disease as a mask of Hodgkin lymphoma
, 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
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The diagnostic challenge of Adult-onset Still’s disease [PDF]
, 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
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Adult-onset Still’s disease with prominent polyserositis
, 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
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Adult Onset Still's Disease and Rocky Mountain Spotted Fever
Case 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
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ADULT-ONSET STILL'S DISEASE TODAY
Научно-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
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Limited diagnostic value of procalcitonin in early diagnosis of adult onset Still’s disease
, 2016 A 17-year-old female patient was referred to the Infectious Diseases Ward because of fever lasting for 14 days. On admission to the hospital the patient was in a generally good state, without any abnormalities on physical examination.
Ewelina Gowin, Jacek Wysocki
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Pure Red Cell Aplasia with Adult Onset Still’s Disease [PDF]
, 2013 Adult Onset Still’s Disease (AOSD) is a rare inflammatory syndrome mostly seen in young adults. Known for its wide range of clinical manifestations, AOSD often presents with nonremitting systemic signs and symptoms.
Mikhael Laskine +3 more
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Therapeutic Apheresis and Dialysis, EarlyView.ABSTRACT Introduction This final analysis of a multicenter, prospective postmarketing surveillance study evaluated the safety of daprodustat in patients with chronic kidney disease anemia in routine clinical practice in Japan. Methods Patients who initiated daprodustat between September 2020 and July 2022 were registered.
Tadao Akizawa +7 more
wiley +1 more source
Adult-Onset Still’s Disease: Delayed Diagnosis Persists [PDF]
, 2023 Adult-onset Still’s disease (AOSD) is a rare inflammatory condition of unknown etiology, that is characterised by quotidian high spiking fever, polyarthritis, evanescent rash, and hyperferritinemia.
Farisya Mohd Lepatoni +1 more
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