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Year Number of Results
1914 1
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1927 2
1928 1
1929 1
1930 1
1931 2
1934 1
1935 2
1936 1
1940 1
1941 1
1945 3
1946 8
1947 4
1948 8
1949 5
1950 7
1951 14
1952 9
1953 8
1954 7
1955 10
1956 12
1957 14
1958 10
1959 10
1960 5
1961 15
1962 28
1963 38
1964 70
1965 58
1966 92
1967 100
1968 94
1969 85
1970 81
1971 92
1972 118
1973 115
1974 140
1975 108
1976 131
1977 173
1978 151
1979 134
1980 136
1981 181
1982 171
1983 191
1984 152
1985 187
1986 233
1987 215
1988 201
1989 203
1990 216
1991 247
1992 215
1993 250
1994 217
1995 208
1996 228
1997 251
1998 275
1999 231
2000 283
2001 293
2002 334
2003 346
2004 317
2005 386
2006 404
2007 437
2008 476
2009 475
2010 517
2011 565
2012 637
2013 620
2014 694
2015 660
2016 697
2017 687
2018 766
2019 778
2020 800
2021 977
2022 968
2023 907
2024 860
2025 405

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19,593 results

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Page 1
Recent advances and evolving concepts in Still's disease.
Ruscitti P, Cantarini L, Nigrovic PA, McGonagle D, Giacomelli R. Ruscitti P, et al. Nat Rev Rheumatol. 2024 Feb;20(2):116-132. doi: 10.1038/s41584-023-01065-6. Epub 2024 Jan 11. Nat Rev Rheumatol. 2024. PMID: 38212542 Review.
Still's disease is a rare inflammatory syndrome that encompasses systemic juvenile idiopathic arthritis and adult-onset Still's disease, both of which can exhibit life-threatening complications, including macrophage activati …
Still's disease is a rare inflammatory syndrome that encompasses systemic juvenile idiopathic arthritis a …
Adult-onset Still's disease in focus: Clinical manifestations, diagnosis, treatment, and unmet needs in the era of targeted therapies.
Efthimiou P, Kontzias A, Hur P, Rodha K, Ramakrishna GS, Nakasato P. Efthimiou P, et al. Semin Arthritis Rheum. 2021 Aug;51(4):858-874. doi: 10.1016/j.semarthrit.2021.06.004. Epub 2021 Jun 13. Semin Arthritis Rheum. 2021. PMID: 34175791 Free article. Review.
BACKGROUND: Adult-onset Still's disease (AOSD) is a rare systemic inflammatory disorder of unknown etiology, characterized by a clinical triad of high spiking fever, arthralgia ( arthritis), and evanescent skin rash. ...In this review, we examined whet …
BACKGROUND: Adult-onset Still's disease (AOSD) is a rare systemic inflammatory disorder of unknown etiology, characteri …
EULAR/PReS recommendations for the diagnosis and management of Still's disease, comprising systemic juvenile idiopathic arthritis and adult-onset Still's disease.
Fautrel B, Mitrovic S, De Matteis A, Bindoli S, Antón J, Belot A, Bracaglia C, Constantin T, Dagna L, Di Bartolo A, Feist E, Foell D, Gattorno M, Georgin-Lavialle S, Giacomelli R, Grom AA, Jamilloux Y, Laskari K, Lazar C, Minoia F, Nigrovic PA, Oliveira Ramos F, Ozen S, Quartier P, Ruscitti P, Sag E, Savic S, Truchetet ME, Vastert SJ, Wilhelmer TC, Wouters C, Carmona L, De Benedetti F. Fautrel B, et al. Ann Rheum Dis. 2024 Nov 14;83(12):1614-1627. doi: 10.1136/ard-2024-225851. Ann Rheum Dis. 2024. PMID: 39317417 Free PMC article.
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. ...A specific concern rose recently with cases of s …
Systemic juvenile idiopathic arthritis (sJIA) and adult-onset Still's disease (AOSD) are considered the s …
Systemic juvenile idiopathic arthritis and adult-onset Still's disease are the same disease: evidence from systematic reviews and meta-analyses informing the 2023 EULAR/PReS recommendations for the diagnosis and management of Still's disease.
De Matteis A, Bindoli S, De Benedetti F, Carmona L, Fautrel B, Mitrovic S. De Matteis A, et al. Ann Rheum Dis. 2024 Nov 14;83(12):1748-1761. doi: 10.1136/ard-2024-225853. Ann Rheum Dis. 2024. PMID: 39317414 Free PMC article.
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. ...
OBJECTIVES: To analyse the similarity in clinical manifestations and laboratory findings between systemic juvenile idiopathic arth …
Efficacy and safety of emapalumab in macrophage activation syndrome.
De Benedetti F, Grom AA, Brogan PA, Bracaglia C, Pardeo M, Marucci G, Eleftheriou D, Papadopoulou C, Schulert GS, Quartier P, Antón J, Laveille C, Frederiksen R, Asnaghi V, Ballabio M, Jacqmin P, de Min C. De Benedetti F, et al. Ann Rheum Dis. 2023 Jun;82(6):857-865. doi: 10.1136/ard-2022-223739. Epub 2023 Mar 31. Ann Rheum Dis. 2023. PMID: 37001971 Free PMC article.
OBJECTIVES: Macrophage activation syndrome (MAS) is a severe, life-threatening complication of systemic juvenile idiopathic arthritis (sJIA) and adult-onset Still's disease (AOSD). The objective of this study was to confirm the adequacy of an em …
OBJECTIVES: Macrophage activation syndrome (MAS) is a severe, life-threatening complication of systemic juvenile idiopathic arthri …
Diagnostics différentiels de la maladie de Castleman.
Viallard JF, Roriz M, Parrens M, Bonnotte B. Viallard JF, et al. Rev Med Interne. 2022 Dec;43(10S1):10S17-10S25. doi: 10.1016/S0248-8663(23)00021-8. Rev Med Interne. 2022. PMID: 36657939 Review. French.
Clinicians are sometimes confronted with the diagnostic difficulties of the idiopathic form of Castleman's Disease (iMCD). As this review reports with demonstrative clinical cases, iMCD can mimic various serious systemic pathologies such as certain autoimmune diseases, …
Clinicians are sometimes confronted with the diagnostic difficulties of the idiopathic form of Castleman's Disease (iMCD). As this re …
Rheumatoid arthritis.
Buchanan WW, Kean CA, Kean WF, Rainsford KD. Buchanan WW, et al. Inflammopharmacology. 2024 Feb;32(1):3-11. doi: 10.1007/s10787-023-01221-0. Epub 2023 May 17. Inflammopharmacology. 2024. PMID: 37195496
Some forms of Juvenile Arthritis are related to adult Rheumatoid Arthritis (aka Still's disease). If untreated Rheumatoid arthritis can result in severe destructive joint damage and often there are associated severe systemic compli …
Some forms of Juvenile Arthritis are related to adult Rheumatoid Arthritis (aka Still's disease). …
Still's disease.
Ansell BM. Ansell BM. Br J Clin Pract. 1991 Autumn;45(3):212-5. Br J Clin Pract. 1991. PMID: 1805920 No abstract available.
Anakinra in children and adults with Still's disease.
Vastert SJ, Jamilloux Y, Quartier P, Ohlman S, Osterling Koskinen L, Kullenberg T, Franck-Larsson K, Fautrel B, de Benedetti F. Vastert SJ, et al. Rheumatology (Oxford). 2019 Nov 1;58(Suppl 6):vi9-vi22. doi: 10.1093/rheumatology/kez350. Rheumatology (Oxford). 2019. PMID: 31769856 Free PMC article. Review.
Systemic juvenile idiopathic arthritis and adult-onset Still's disease are rare autoinflammatory disorders with common features, supporting the recognition of these being one disease-Still's disease-with different age …
Systemic juvenile idiopathic arthritis and adult-onset Still's disease are rare autoinflammatory disorder …
[Still's disease in children and adults].
Hedrich CM, Günther C, Aringer M. Hedrich CM, et al. Z Rheumatol. 2017 Sep;76(7):595-608. doi: 10.1007/s00393-017-0358-5. Z Rheumatol. 2017. PMID: 28755070 Review. German.
Systemic juvenile idiopathic arthritis (sJIA) is characterized by fever, arthritis, and other signs of systemic inflammation. Historically, sJIA was named Still's disease after George Frederic Still, who first reported patients. Individua …
Systemic juvenile idiopathic arthritis (sJIA) is characterized by fever, arthritis, and other signs of systemic inflamm …
19,593 results
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