Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1914 1
1921 1
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 696
2017 688
2018 766
2019 780
2020 794
2021 975
2022 998
2023 123
Text availability
Article attribute
Article type
Publication date

Search Results

17,838 results
Results by year
Filters applied: . Clear all
Page 1
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 …
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. Management of AOSD poses several ch …
BACKGROUND: Adult-onset Still's disease (AOSD) is a rare systemic inflammatory disorder of unknown etiology, characteri …
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 diseas …
Clinicians are sometimes confronted with the diagnostic difficulties of the idiopathic form of Castleman's Disease (iMCD). As …
Disparities in the prevalence of clinical features between systemic juvenile idiopathic arthritis and adult-onset Still's disease.
Ruscitti P, Natoli V, Consolaro A, Caorsi R, Rosina S, Giancane G, Naddei R, Di Cola I, Di Muzio C, Berardicurti O, Iacono D, Pantano I, Rozza G, Rossi S, De Stefano L, Balduzzi S, Vitale A, Caso F, Costa L, Prete M, Navarini L, Iagnocco A, Atzeni F, Guggino G, Perosa F, Cantarini L, Frediani B, Montecucco C, Ciccia F, Cipriani P, Gattorno M, Giacomelli R, Ravelli A. Ruscitti P, et al. Rheumatology (Oxford). 2022 Oct 6;61(10):4124-4129. doi: 10.1093/rheumatology/keac027. Rheumatology (Oxford). 2022. PMID: 35078234 Free PMC article.
OBJECTIVE: To compare clinical features and treatments of patients with systemic JIA (sIJA) and adult-onset Still's disease (AOSD). METHODS: The clinical charts of consecutive patients with sJIA by International League of Association of Rheumatology criteria …
OBJECTIVE: To compare clinical features and treatments of patients with systemic JIA (sIJA) and adult-onset Still's disease
[A better understanding of juvenile idiopathic arthritis with classification criteria].
Akioka S. Akioka S. Nihon Rinsho Meneki Gakkai Kaishi. 2016;39(6):513-521. doi: 10.2177/jsci.39.513. Nihon Rinsho Meneki Gakkai Kaishi. 2016. PMID: 28049960 Free article. Review. Japanese.
Juvenile idiopathic arthritis, JIA, is a novel rheumatic disease in childhood introduced by the International League of Associations for Rheumatology. It is defined as a chronic, inflammatory disorder of unknown etiology, which is classified into seven catego
Juvenile idiopathic arthritis, JIA, is a novel rheumatic disease in childhood introduced by the International League of
[Still's disease in children and adults].
Hedrich CM, Günther C, Aringer M. Hedrich CM, et al. Hautarzt. 2017 Jun;68(6):497-511. doi: 10.1007/s00105-017-3983-7. Hautarzt. 2017. PMID: 28451698 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. .. …
Systemic juvenile idiopathic arthritis (sJIA) is characterized by fever, arthritis, and other signs of systemic inflamm …
[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. .. …
Systemic juvenile idiopathic arthritis (sJIA) is characterized by fever, arthritis, and other signs of systemic inflamm …
Cardiac tamponade in Still disease: a review of the literature.
Parvez N, Carpenter JL. Parvez N, et al. South Med J. 2009 Aug;102(8):832-7. doi: 10.1097/SMJ.0b013e3181ad4847. South Med J. 2009. PMID: 19593288 Review.
Adult onset Still disease is an unusual multisystem inflammatory disorder of unknown etiology and pathogenesis. ...Cardiac tamponade is a rare complication of pericarditis occurring in the context of Still disease. We conducted a review of the English …
Adult onset Still disease is an unusual multisystem inflammatory disorder of unknown etiology and pathogenesis. ...Cardiac tam …
[Adult Still's disease].
Matsumoto Y. Matsumoto Y. Ryumachi. 1986 Feb;26(1):51-9. Ryumachi. 1986. PMID: 3520880 Review. Japanese. No abstract available.
Canakinumab for the treatment of adult-onset Still's disease.
Sfriso P, Bindoli S, Doria A, Feist E, Galozzi P. Sfriso P, et al. Expert Rev Clin Immunol. 2020 Feb;16(2):129-138. doi: 10.1080/1744666X.2019.1707664. Epub 2020 Jan 18. Expert Rev Clin Immunol. 2020. PMID: 31957508 Review.
Introduction: Adult-onset Still's disease (AOSD) is a rare multisystem autoinflammatory disorder of unknown etiology, with clinical and biological similarities with the juvenile form (sJIA).The pivotal role of interleukin (IL)-1 gives rise to the use o …
Introduction: Adult-onset Still's disease (AOSD) is a rare multisystem autoinflammatory disorder of unknown etiology, w …
17,838 results
You have reached the last available page of results. Please see the User Guide for more information.