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

Year Number of Results
1946 10
1947 6
1948 8
1949 4
1950 6
1951 6
1952 6
1953 8
1954 4
1955 9
1956 7
1957 11
1958 16
1959 6
1960 9
1961 15
1962 14
1963 26
1964 36
1965 38
1966 18
1967 31
1968 40
1969 46
1970 54
1971 78
1972 56
1973 59
1974 59
1975 48
1976 86
1977 80
1978 99
1979 83
1980 103
1981 94
1982 137
1983 102
1984 124
1985 156
1986 150
1987 120
1988 146
1989 154
1990 147
1991 140
1992 137
1993 153
1994 149
1995 144
1996 196
1997 214
1998 201
1999 230
2000 227
2001 269
2002 268
2003 404
2004 300
2005 354
2006 354
2007 356
2008 403
2009 394
2010 395
2011 407
2012 455
2013 527
2014 585
2015 569
2016 522
2017 497
2018 539
2019 606
2020 663
2021 700
2022 417
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Search Results

13,027 results
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Page 1
Behçet disease: New aspects.
Bulur I, Onder M. Bulur I, et al. Clin Dermatol. 2017 Sep-Oct;35(5):421-434. doi: 10.1016/j.clindermatol.2017.06.004. Epub 2017 Jun 27. Clin Dermatol. 2017. PMID: 28916023 Review.
Behcet disease is currently considered an "autoinflammatory disease" triggered by infection and environmental factors in genetically predisposed individuals. ...It is important to evaluate the patient with complex aphthosis for Behcet disease an
Behcet disease is currently considered an "autoinflammatory disease" triggered by infection and environmental factors i
Behçet's disease.
Davatchi F. Davatchi F. Int J Rheum Dis. 2018 Dec;21(12):2057-2058. doi: 10.1111/1756-185X.13465. Int J Rheum Dis. 2018. PMID: 30681276 No abstract available.
Gastrointestinal Behçet's disease: a review.
Skef W, Hamilton MJ, Arayssi T. Skef W, et al. World J Gastroenterol. 2015 Apr 7;21(13):3801-12. doi: 10.3748/wjg.v21.i13.3801. World J Gastroenterol. 2015. PMID: 25852265 Free PMC article. Review.
Behcet's disease (BD) is an idiopathic, chronic, relapsing, multi-systemic vasculitis characterized by recurrent oral and genital aphthous ulcers, ocular disease and skin lesions. ...By comparison, the prevalence in North American and Northern European countr
Behcet's disease (BD) is an idiopathic, chronic, relapsing, multi-systemic vasculitis characterized by recurrent oral and geni
Immunopathogenesis of Behçet Disease.
Nieto IG, Alabau JLC. Nieto IG, et al. Curr Rheumatol Rev. 2020;16(1):12-20. doi: 10.2174/1573397115666190415142426. Curr Rheumatol Rev. 2020. PMID: 30987569 Review.
BACKGROUND: Behcet's Disease (BD, OMIM 109650) is a chronic relapsing inflammatory disease of unknown etiology with unpredictable exacerbations and remissions. First described in 1937 by the Turkish dermatologist HulusiBehcet, as a trisympton complex (oral an …
BACKGROUND: Behcet's Disease (BD, OMIM 109650) is a chronic relapsing inflammatory disease of unknown etiology with unp …
Intestinal Behçet and Crohn's disease: two sides of the same coin.
Valenti S, Gallizzi R, De Vivo D, Romano C. Valenti S, et al. Pediatr Rheumatol Online J. 2017 Apr 20;15(1):33. doi: 10.1186/s12969-017-0162-4. Pediatr Rheumatol Online J. 2017. PMID: 28427473 Free PMC article. Review.
Behcet's disease (BD) and Crohn's disease (CD) are chronic immune-mediated, inflammatory disorders affecting many different systems (joints, skin, eyes, gastrointestinal and biliary tracts). ...A comprehensive search of published literature using the Pubmed (
Behcet's disease (BD) and Crohn's disease (CD) are chronic immune-mediated, inflammatory disorders affecting many diffe
One year in review 2020: Behçet's syndrome.
Hatemi G, Seyahi E, Fresko I, Talarico R, Hamuryudan V. Hatemi G, et al. Clin Exp Rheumatol. 2020 Sep-Oct;38 Suppl 127(5):3-10. Epub 2020 Dec 10. Clin Exp Rheumatol. 2020. PMID: 33331271 Free article. Review.
Behcet's syndrome is a variable vessel vasculitis with multi-system involvement that shows important heterogeneity among patients regarding demographic features, organ manifestations, frequency and severity of relapses, disease course, response to treatment a
Behcet's syndrome is a variable vessel vasculitis with multi-system involvement that shows important heterogeneity among patie
Behçet's disease.
Saadoun D, Wechsler B. Saadoun D, et al. Orphanet J Rare Dis. 2012 Apr 12;7:20. doi: 10.1186/1750-1172-7-20. Orphanet J Rare Dis. 2012. PMID: 22497990 Free PMC article. Review.
DEFINITION OF THE DISEASE: Behcet disease (BD) is a chronic, relapsing, multisystemic disorder characterized by mucocutaneous, ocular, vascular and central nervous system manifestations. ...DIFFERRENTIAL DIAGNOSIS: It depends on the clinical presentation of B …
DEFINITION OF THE DISEASE: Behcet disease (BD) is a chronic, relapsing, multisystemic disorder characterized by mucocut …
Behçet syndrome.
Yazici Y, Hatemi G, Bodaghi B, Cheon JH, Suzuki N, Ambrose N, Yazici H. Yazici Y, et al. Nat Rev Dis Primers. 2021 Sep 16;7(1):67. doi: 10.1038/s41572-021-00301-1. Nat Rev Dis Primers. 2021. PMID: 34531393 Review.
The presence of symptom clusters, regional differences in disease expression and similarities with, for example, Crohn's disease suggest that multiple pathological pathways are involved in Behcet syndrome. ...Furthermore, even with our incomplete under …
The presence of symptom clusters, regional differences in disease expression and similarities with, for example, Crohn's disease
[Behçet's disease].
Mahr A. Mahr A. Ther Umsch. 2022 Jun;79(5):269-276. doi: 10.1024/0040-5930/a001354. Ther Umsch. 2022. PMID: 35583026 German.
Behcet's disease Abstract. Behcet's disease (BD) represents a diagnostic and therapeutic challenge for the treating physician. The rarity of the disease and its heterogeneous clinical presentations hamper physicians in easily gaining knowledge a
Behcet's disease Abstract. Behcet's disease (BD) represents a diagnostic and therapeutic challenge for the treat
Behcet's Disease.
Williams DS. Williams DS. J Insur Med. 2019;48(1):103-105. doi: 10.17849/insm-48-1-1-3.1. Epub 2019 Jun 13. J Insur Med. 2019. PMID: 31194600
Behcet's disease is a rare systemic vasculitis disorder of unknown etiology characterized by recurrent attacks of acute inflammation affecting multiple parts of the body....
Behcet's disease is a rare systemic vasculitis disorder of unknown etiology characterized by recurrent attacks of acute inflam
13,027 results
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