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A comprehensive review on adult onset Still's disease.
Journal of Autoimmunity, 2018Adult-onset Still's disease (AOSD) is a systemic inflammatory disorder of unknown etiology usually affecting young adults; spiking fever, arthritis and evanescent rash are commonly observed during the disease.
R. Giacomelli, P. Ruscitti, Y. Shoenfeld
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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
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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
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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
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Annals of the Rheumatic Diseases
Systemic juvenile idiopathic arthritis (sJIA) and adult-onset Still’s disease (AOSD) are considered the same disease, but a common approach for diagnosis and management is still missing. Methods In May 2022, EULAR and PReS endorsed a proposal for a joint
B. Fautrel +32 more
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Systemic juvenile idiopathic arthritis (sJIA) and adult-onset Still’s disease (AOSD) are considered the same disease, but a common approach for diagnosis and management is still missing. Methods In May 2022, EULAR and PReS endorsed a proposal for a joint
B. Fautrel +32 more
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Medicina Clínica (English Edition), 2018
Adult onset Still's disease is a rare systemic condition at the crossroads between auto-inflammatory syndromes and autoimmune diseases, with considerable heterogeneity in terms of clinical presentation, evolution and severity. This article reviews the main advances and lesser known aspects of this entity related to its clinical spectrum (atypical ...
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Adult onset Still's disease is a rare systemic condition at the crossroads between auto-inflammatory syndromes and autoimmune diseases, with considerable heterogeneity in terms of clinical presentation, evolution and severity. This article reviews the main advances and lesser known aspects of this entity related to its clinical spectrum (atypical ...
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Annals of the Rheumatic Diseases
Objectives To analyse the similarity in clinical manifestations and laboratory findings between systemic juvenile idiopathic arthritis (sJIA) and adult-onset Still’s disease (AOSD). Methods Three systematic reviews (SR) were performed.
A. de Matteis +5 more
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Objectives To analyse the similarity in clinical manifestations and laboratory findings between systemic juvenile idiopathic arthritis (sJIA) and adult-onset Still’s disease (AOSD). Methods Three systematic reviews (SR) were performed.
A. de Matteis +5 more
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Best Practice & Research Clinical Rheumatology, 2008
Adult-onset Still disease (AOSD) is an uncommon inflammatory condition of unknown origin typically characterized by four main (cardinal) symptoms: spiking fever > or =39 degrees C, arthralgia or arthritis, skin rash and hyperleucocytosis (> or =10,000 cells/mm3) with neutrophils > or =80%.
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Adult-onset Still disease (AOSD) is an uncommon inflammatory condition of unknown origin typically characterized by four main (cardinal) symptoms: spiking fever > or =39 degrees C, arthralgia or arthritis, skin rash and hyperleucocytosis (> or =10,000 cells/mm3) with neutrophils > or =80%.
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The Journal of the Association of Physicians of India, 2022
Adult onset Still's disease (AOSD) is a rare systemic inflammatory disorder of unknown aetiology, characterised by daily spiking high fevers accompanied by rash, arthritis, and systemic manifestations. There are no specific diagnostic tests for AOSD.
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Adult onset Still's disease (AOSD) is a rare systemic inflammatory disorder of unknown aetiology, characterised by daily spiking high fevers accompanied by rash, arthritis, and systemic manifestations. There are no specific diagnostic tests for AOSD.
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Arthritis & Rheumatism, 1987
AbstractWe reviewed the long‐term natural history of 21 adult‐onset Still's disease patients. Patient subsets were identified according to clinical course patterns. These included monocyclic systemic disease in 4, polycyclic systemic disease in 2, chronic articular monocyclic systemic disease in 10, and chronic articular polycyclic systemic disease in ...
John J. Cush +4 more
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AbstractWe reviewed the long‐term natural history of 21 adult‐onset Still's disease patients. Patient subsets were identified according to clinical course patterns. These included monocyclic systemic disease in 4, polycyclic systemic disease in 2, chronic articular monocyclic systemic disease in 10, and chronic articular polycyclic systemic disease in ...
John J. Cush +4 more
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