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Results by year

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

Year Number of Results
1966 1
1967 2
1968 4
1969 2
1970 3
1971 3
1972 3
1973 2
1974 6
1975 4
1976 7
1977 7
1978 8
1979 3
1980 3
1981 9
1982 1
1983 5
1984 5
1985 11
1986 12
1987 7
1988 15
1989 24
1990 17
1991 24
1992 19
1993 24
1994 19
1995 24
1996 35
1997 38
1998 26
1999 28
2000 28
2001 31
2002 29
2003 28
2004 25
2005 44
2006 37
2007 29
2008 44
2009 51
2010 49
2011 48
2012 50
2013 50
2014 70
2015 57
2016 43
2017 48
2018 60
2019 54
2020 65
2021 66
2022 69
2023 57

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Search Results

1,413 results

Results by year

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Page 1
Review: Ewing Sarcoma Predisposition.
Gargallo P, Yáñez Y, Juan A, Segura V, Balaguer J, Torres B, Oltra S, Castel V, Cañete A. Gargallo P, et al. Pathol Oncol Res. 2020 Oct;26(4):2057-2066. doi: 10.1007/s12253-019-00765-3. Epub 2019 Oct 26. Pathol Oncol Res. 2020. PMID: 31656020 Free article. Review.
Ewing sarcoma is a rare tumor developed in bone and soft tissues of children and teenagers. ...This review summarizes the available evidence on predisposing factors involved in Ewing sarcoma susceptibility. On the basis of these data, an integrated app
Ewing sarcoma is a rare tumor developed in bone and soft tissues of children and teenagers. ...This review summarizes the avai
Ewing sarcoma and Ewing-like tumors.
Sbaraglia M, Righi A, Gambarotti M, Dei Tos AP. Sbaraglia M, et al. Virchows Arch. 2020 Jan;476(1):109-119. doi: 10.1007/s00428-019-02720-8. Epub 2019 Dec 4. Virchows Arch. 2020. PMID: 31802230 Review.
Ewing sarcoma (ES) and Ewing-like sarcomas are highly aggressive round cell mesenchymal neoplasms, most often occurring in children and young adults. ...A combination of morphologic, immunohistochemical, and molecular findings allows accurate classification i
Ewing sarcoma (ES) and Ewing-like sarcomas are highly aggressive round cell mesenchymal neoplasms, most often occurring
Bone Cancer: Diagnosis and Treatment Principles.
Ferguson JL, Turner SP. Ferguson JL, et al. Am Fam Physician. 2018 Aug 15;98(4):205-213. Am Fam Physician. 2018. PMID: 30215968 Free article. Review.
Primary bone cancers include osteosarcoma, Ewing sarcoma, and chondrosarcoma. They account for less than 1% of diagnosed cancers each year and are associated with significant morbidity and mortality. ...Prognosis for osteosarcoma and Ewing sarcoma depe …
Primary bone cancers include osteosarcoma, Ewing sarcoma, and chondrosarcoma. They account for less than 1% of diagnosed cance …
Diagnosis and treatment of Ewing sarcoma of the bone: a review article.
Ozaki T. Ozaki T. J Orthop Sci. 2015 Mar;20(2):250-63. doi: 10.1007/s00776-014-0687-z. Epub 2015 Feb 19. J Orthop Sci. 2015. PMID: 25691401 Free PMC article. Review.
Ewing sarcoma (ES) is rare in Japanese people, and only 30-40 patients develop the disease annually. ...
Ewing sarcoma (ES) is rare in Japanese people, and only 30-40 patients develop the disease annually. ...
Ewing sarcoma.
Grünewald TGP, Cidre-Aranaz F, Surdez D, Tomazou EM, de Álava E, Kovar H, Sorensen PH, Delattre O, Dirksen U. Grünewald TGP, et al. Nat Rev Dis Primers. 2018 Jul 5;4(1):5. doi: 10.1038/s41572-018-0003-x. Nat Rev Dis Primers. 2018. PMID: 29977059 Review.
Ewing sarcoma is the second most frequent bone tumour of childhood and adolescence that can also arise in soft tissue. Ewing sarcoma is a highly aggressive cancer, with a survival of 70-80% for patients with standard-risk and localized disease and ~30%
Ewing sarcoma is the second most frequent bone tumour of childhood and adolescence that can also arise in soft tissue. Ewin
Ewing sarcoma.
Eaton BR, Claude L, Indelicato DJ, Vatner R, Yeh B, Schwarz R, Laack N. Eaton BR, et al. Pediatr Blood Cancer. 2021 May;68 Suppl 2:e28355. doi: 10.1002/pbc.28355. Pediatr Blood Cancer. 2021. PMID: 33818887 Review.
Ewing sarcoma is a rare tumor that requires complex multidisciplinary management. ...
Ewing sarcoma is a rare tumor that requires complex multidisciplinary management. ...
Ewing's sarcoma.
Balamuth NJ, Womer RB. Balamuth NJ, et al. Lancet Oncol. 2010 Feb;11(2):184-92. doi: 10.1016/S1470-2045(09)70286-4. Lancet Oncol. 2010. PMID: 20152770 Review.
Progress in the treatment of Ewing's sarcoma, the second most common bone tumour in children and adolescents, has improved survival from about 10% in the period before chemotherapy was introduced to about 75% today for patients with localised tumours. ...Molecular t …
Progress in the treatment of Ewing's sarcoma, the second most common bone tumour in children and adolescents, has improved sur …
Ewing Sarcoma: Current Management and Future Approaches Through Collaboration.
Gaspar N, Hawkins DS, Dirksen U, Lewis IJ, Ferrari S, Le Deley MC, Kovar H, Grimer R, Whelan J, Claude L, Delattre O, Paulussen M, Picci P, Sundby Hall K, van den Berg H, Ladenstein R, Michon J, Hjorth L, Judson I, Luksch R, Bernstein ML, Marec-Bérard P, Brennan B, Craft AW, Womer RB, Juergens H, Oberlin O. Gaspar N, et al. J Clin Oncol. 2015 Sep 20;33(27):3036-46. doi: 10.1200/JCO.2014.59.5256. Epub 2015 Aug 24. J Clin Oncol. 2015. PMID: 26304893 Review.
Ewing sarcoma (ES) is an aggressive sarcoma of bone and soft tissue occurring at any age with a peak incidence in adolescents and young adults. ...
Ewing sarcoma (ES) is an aggressive sarcoma of bone and soft tissue occurring at any age with a peak incidence in adole
Ewing sarcoma in an infant and review of the literature.
Bedük-Esen ÇS, Gültekin M, Aydın GB, Akyüz C, Oğuz KK, Orhan D, Cengiz M, Gürkaynak M, Yıldız F. Bedük-Esen ÇS, et al. Turk J Pediatr. 2019;61(5):760-764. doi: 10.24953/turkjped.2019.05.016. Turk J Pediatr. 2019. PMID: 32105009 Free article. Review.
Beduk Esen CS, Gultekin M, Aydin GB, Akyuz C, Karli Oguz K, Orhan D, Cengiz M, Gurkaynak M, Yildiz F. Ewing sarcoma in an infant and review of the literature. Turk J Pediatr 2019; 61: 760-764. Ewing sarcoma (ES) is a rare tumor in infants and prognosis …
Beduk Esen CS, Gultekin M, Aydin GB, Akyuz C, Karli Oguz K, Orhan D, Cengiz M, Gurkaynak M, Yildiz F. Ewing sarcoma in an infa …
Ewing sarcoma.
Choi EY, Gardner JM, Lucas DR, McHugh JB, Patel RM. Choi EY, et al. Semin Diagn Pathol. 2014 Jan;31(1):39-47. doi: 10.1053/j.semdp.2014.01.002. Epub 2014 Jan 5. Semin Diagn Pathol. 2014. PMID: 24680181 Review.
The purpose of this article is to review the clinical, radiological, histologic, and molecular features of Ewing sarcoma and to provide a discussion of the differential diagnosis of small round cell tumors of bone....
The purpose of this article is to review the clinical, radiological, histologic, and molecular features of Ewing sarcoma and t …
1,413 results