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

Year Number of Results
1964 3
1965 1
1966 1
1969 1
1970 2
1971 2
1973 5
1974 2
1975 5
1976 3
1977 3
1978 6
1979 2
1980 4
1981 6
1982 2
1983 6
1984 3
1985 2
1986 8
1987 9
1988 13
1989 15
1990 26
1991 16
1992 30
1993 24
1994 29
1995 24
1996 17
1997 24
1998 32
1999 28
2000 49
2001 29
2002 57
2003 62
2004 52
2005 54
2006 62
2007 50
2008 71
2009 65
2010 66
2011 74
2012 91
2013 73
2014 78
2015 86
2016 94
2017 81
2018 81
2019 83
2020 104
2021 74
2022 65
2023 72
2024 22

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1,903 results

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Page 1
Periodic fever syndromes.
Lachmann HJ. Lachmann HJ. Best Pract Res Clin Rheumatol. 2017 Aug;31(4):596-609. doi: 10.1016/j.berh.2017.12.001. Epub 2018 Jan 11. Best Pract Res Clin Rheumatol. 2017. PMID: 29773275 Review.
Periodic fever syndromes are autoinflammatory diseases. The majority present in infancy or childhood and are characterised by recurrent episodes of fever and systemic inflammation that occur in the absence of autoantibody production or identifiable infection. …
Periodic fever syndromes are autoinflammatory diseases. The majority present in infancy or childhood and are characterised by …
Classification criteria for autoinflammatory recurrent fevers.
Gattorno M, Hofer M, Federici S, Vanoni F, Bovis F, Aksentijevich I, Anton J, Arostegui JI, Barron K, Ben-Cherit E, Brogan PA, Cantarini L, Ceccherini I, De Benedetti F, Dedeoglu F, Demirkaya E, Frenkel J, Goldbach-Mansky R, Gul A, Hentgen V, Hoffman H, Kallinich T, Kone-Paut I, Kuemmerle-Deschner J, Lachmann HJ, Laxer RM, Livneh A, Obici L, Ozen S, Rowczenio D, Russo R, Shinar Y, Simon A, Toplak N, Touitou I, Uziel Y, van Gijn M, Foell D, Garassino C, Kastner D, Martini A, Sormani MP, Ruperto N; Eurofever Registry and the Paediatric Rheumatology International Trials Organisation (PRINTO). Gattorno M, et al. Ann Rheum Dis. 2019 Aug;78(8):1025-1032. doi: 10.1136/annrheumdis-2019-215048. Epub 2019 Apr 24. Ann Rheum Dis. 2019. PMID: 31018962 Review.
BACKGROUND: Different diagnostic and classification criteria are available for hereditary recurrent fevers (HRF)-familial Mediterranean fever (FMF), tumour necrosis factor receptor-associated periodic fever syndrome (TRAPS), mevalonate kinase deficienc …
BACKGROUND: Different diagnostic and classification criteria are available for hereditary recurrent fevers (HRF)-familial Mediterrane …
Autoinflammatory Diseases/Periodic Fevers.
Schutt C, Siegel DM. Schutt C, et al. Pediatr Rev. 2023 Sep 1;44(9):481-490. doi: 10.1542/pir.2022-005635. Pediatr Rev. 2023. PMID: 37653132 Review.
Most patients will have self-limited, benign infectious illnesses. However, the possibility of a periodic fever syndrome should be considered if febrile episodes become recurrent over an extended period and are associated with particular signs and symptoms du …
Most patients will have self-limited, benign infectious illnesses. However, the possibility of a periodic fever syndrome shoul …
Fever of unknown origin (FUO) revised.
Unger M, Karanikas G, Kerschbaumer A, Winkler S, Aletaha D. Unger M, et al. Wien Klin Wochenschr. 2016 Nov;128(21-22):796-801. doi: 10.1007/s00508-016-1083-9. Epub 2016 Sep 26. Wien Klin Wochenschr. 2016. PMID: 27670857 Free PMC article. Review.
Fever of unknown origin (FUO) was originally characterised in 1961 by Petersdorf and Beeson as a disease condition of temperature exceeding 38.3 C on at least three occasions over a period of at least three weeks, with no diagnosis made despite one week of inpatient …
Fever of unknown origin (FUO) was originally characterised in 1961 by Petersdorf and Beeson as a disease condition of temperature exc …
Neutrophilic urticarial dermatosis: A review.
Gusdorf L, Lipsker D. Gusdorf L, et al. Ann Dermatol Venereol. 2018 Dec;145(12):735-740. doi: 10.1016/j.annder.2018.06.010. Epub 2018 Sep 14. Ann Dermatol Venereol. 2018. PMID: 30224079 Review.
The elementary lesion lasts 24 to 48hours and resolves without leaving any residual pigmentation. Extra-cutaneous signs are common, particularly fever or arthralgia. At histopathology, the dermis contains dense neutrophilic interstitial infiltrate with leukocytoclasis, but …
The elementary lesion lasts 24 to 48hours and resolves without leaving any residual pigmentation. Extra-cutaneous signs are common, particul …
PFAPA syndrome: a review on treatment and outcome.
Vanoni F, Theodoropoulou K, Hofer M. Vanoni F, et al. Pediatr Rheumatol Online J. 2016 Jun 27;14(1):38. doi: 10.1186/s12969-016-0101-9. Pediatr Rheumatol Online J. 2016. PMID: 27349388 Free PMC article. Review.
The syndrome of periodic fever, aphthous stomatitis, pharyngitis and cervical adenitis (PFAPA syndrome) is the most common cause of periodic fever in childhood. The current pharmacological treatment includes corticosteroids, which usually are efficacio …
The syndrome of periodic fever, aphthous stomatitis, pharyngitis and cervical adenitis (PFAPA syndrome) is the most common cau …
Human Influenza Epidemiology.
Ryu S, Cowling BJ. Ryu S, et al. Cold Spring Harb Perspect Med. 2021 Dec 1;11(12):a038356. doi: 10.1101/cshperspect.a038356. Cold Spring Harb Perspect Med. 2021. PMID: 32988982 Free PMC article. Review.
Most influenza virus infections cause mild and self-limiting disease, and around one-half of all infections occur with a fever. Only a small minority of infections lead to serious disease requiring hospitalization. ...
Most influenza virus infections cause mild and self-limiting disease, and around one-half of all infections occur with a fever. Only …
Systemic autoinflammatory diseases: Clinical state of the art.
Georgin-Lavialle S, Ducharme-Benard S, Sarrabay G, Savey L, Grateau G, Hentgen V. Georgin-Lavialle S, et al. Best Pract Res Clin Rheumatol. 2020 Aug;34(4):101529. doi: 10.1016/j.berh.2020.101529. Epub 2020 Jun 13. Best Pract Res Clin Rheumatol. 2020. PMID: 32546426 Free article. Review.
The four historical monogenic diseases are familial Mediterranean fever (associated with MEFV mutations), cryopyrinopathies (NLRP3 mutations), tumor necrosis factor receptor-associated periodic syndrome (TNFRSF1A mutations), and mevalonate kinase deficiency (MVK mut …
The four historical monogenic diseases are familial Mediterranean fever (associated with MEFV mutations), cryopyrinopathies (NLRP3 mu …
Revisiting TNF Receptor-Associated Periodic Syndrome (TRAPS): Current Perspectives.
Cudrici C, Deuitch N, Aksentijevich I. Cudrici C, et al. Int J Mol Sci. 2020 May 5;21(9):3263. doi: 10.3390/ijms21093263. Int J Mol Sci. 2020. PMID: 32380704 Free PMC article. Review.
Tumor necrosis factor receptor-associated periodic syndrome (TRAPS) is an autosomal dominant autoinflammatory syndrome characterized by prolonged and recurrent episodes of fever, abdominal and/or chest pain, arthralgia, myalgia, and erythematous rash. ...
Tumor necrosis factor receptor-associated periodic syndrome (TRAPS) is an autosomal dominant autoinflammatory syndrome characterized …
Overview of fever of unknown origin in adult and paediatric patients.
Attard L, Tadolini M, De Rose DU, Cattalini M. Attard L, et al. Clin Exp Rheumatol. 2018 Jan-Feb;36 Suppl 110(1):10-24. Epub 2018 May 3. Clin Exp Rheumatol. 2018. PMID: 29742054 Free article. Review.
Fever of unknown origin (FUO) can be caused by a wide group of diseases, and can include both benign and serious conditions. ...We also provide a comprehensive account of specific signs and symptoms that could suggest possible diagnoses and guide the work-up of FUO and non …
Fever of unknown origin (FUO) can be caused by a wide group of diseases, and can include both benign and serious conditions. ...We al …
1,903 results