Results 241 to 250 of about 4,398 (288)
Macrophage Activation Syndrome/Secondary Hemophagocytic Lymphohistiocytosis in Adult-Onset Still's Disease: An Uncommon Initial Presentation in a Young Nepalese Female: A Case Report. [PDF]
Clin Case RepBishwakarma K +3 more
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The diagnostic dilemma of adult-onset Still's disease: a case report. [PDF]
Ann Med Surg (Lond)Yadav MK +5 more
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Adult Still’s Disease Complicated by Macrophage Activation Syndrome [PDF]
, 2017 Saito, Ashley, Williams, Jason
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Adult-onset Still's disease during pregnancy: two case reports and a comprehensive literature review. [PDF]
Front Med (Lausanne)Xu W +8 more
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[Adult-onset Still's disease].
Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine, 1993 openaire +1 more source
Adult-Onset Still's Disease Mimicking Myositis: A Case Report. [PDF]
CureusPrado MB, Adiao KJB.
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High Neutrophil Alkaline Phosphatase Activity in Adult-Onset Still's Disease. [PDF]
Rheumatol TherDing N +14 more
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Best Practice & Research Clinical Rheumatology, 2004
Adult-onset Still's disease (AOSD) is a systemic inflammatory disorder of unknown etiology and pathogenesis. AOSD is a rare condition, usually presenting with high fever accompanied by systemic manifestations. The disease is a heterogeneous pathological entity with a range of etiologies, manifestations and prognosis.
János, Kádár, Edina, Petrovicz
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Adult-onset Still's disease (AOSD) is a systemic inflammatory disorder of unknown etiology and pathogenesis. AOSD is a rare condition, usually presenting with high fever accompanied by systemic manifestations. The disease is a heterogeneous pathological entity with a range of etiologies, manifestations and prognosis.
János, Kádár, Edina, Petrovicz
openaire +2 more sources
Clinical Rheumatology, 1989
Three patients with adult onset of Still's disease are presented. Common early findings were: septic fever, polyarthralgia, leukocytosis, neutrophilia and elevated sedimentation rate. All of them had abnormal liver function tests which returned to normal values following corticosteroid therapy.
N, Arber +4 more
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Three patients with adult onset of Still's disease are presented. Common early findings were: septic fever, polyarthralgia, leukocytosis, neutrophilia and elevated sedimentation rate. All of them had abnormal liver function tests which returned to normal values following corticosteroid therapy.
N, Arber +4 more
openaire +2 more sources
Baillière's Clinical Rheumatology, 1991
Adult onset Still's disease seems to be the adult form of Still's disease in children. The key symptoms of the disease are high spiking fever, arthritis and a macular or maculopapular, salmon-pink evanescent rash, almost always accompanied by neutrophilic leukocytosis and frequently by sore throat, intense myalgias, lymphadenopathy, splenomegaly and ...
L B, van de Putte, J M, Wouters
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Adult onset Still's disease seems to be the adult form of Still's disease in children. The key symptoms of the disease are high spiking fever, arthritis and a macular or maculopapular, salmon-pink evanescent rash, almost always accompanied by neutrophilic leukocytosis and frequently by sore throat, intense myalgias, lymphadenopathy, splenomegaly and ...
L B, van de Putte, J M, Wouters
openaire +2 more sources