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Results by year

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

Year Number of Results
1964 1
1967 1
1968 1
1971 3
1972 1
1974 3
1975 1
1976 3
1977 3
1978 8
1979 1
1980 1
1981 3
1983 5
1984 2
1985 10
1986 9
1987 4
1988 12
1989 11
1990 6
1991 14
1992 23
1993 20
1994 17
1995 16
1996 16
1997 10
1998 15
1999 15
2000 16
2001 12
2002 9
2003 16
2004 17
2005 12
2006 13
2007 12
2008 22
2009 27
2010 18
2011 19
2012 34
2013 29
2014 22
2015 17
2016 18
2017 25
2018 17
2019 35
2020 19
2021 15
2022 28
2023 18
2024 4

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Search Results

652 results

Results by year

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Page 1
Childhood rhabdomyosarcoma.
Córdoba Rovira SM, Inarejos Clemente EJ. Córdoba Rovira SM, et al. Radiologia. 2016 Nov-Dec;58(6):481-490. doi: 10.1016/j.rx.2016.09.003. Epub 2016 Nov 1. Radiologia. 2016. PMID: 27810092 Free article. Review. English, Spanish.
Rhabdomyosarcoma is the most common soft-tissue sarcoma in children; it can appear in any part of the body. Its biological behavior varies widely, and despite the absence of specific clinical or radiological characteristics, rhabdomyosarcoma should be taken into account in …
Rhabdomyosarcoma is the most common soft-tissue sarcoma in children; it can appear in any part of the body. Its biological behavior v …
Osteosarcoma.
Beird HC, Bielack SS, Flanagan AM, Gill J, Heymann D, Janeway KA, Livingston JA, Roberts RD, Strauss SJ, Gorlick R. Beird HC, et al. Nat Rev Dis Primers. 2022 Dec 8;8(1):77. doi: 10.1038/s41572-022-00409-y. Nat Rev Dis Primers. 2022. PMID: 36481668 Free article. Review.
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% for th …
Ewing sarcoma is the second most frequent bone tumour of childhood and adolescence that can also arise in soft tissue. Ewing …
The epidemiology of osteosarcoma.
Ottaviani G, Jaffe N. Ottaviani G, et al. Cancer Treat Res. 2009;152:3-13. doi: 10.1007/978-1-4419-0284-9_1. Cancer Treat Res. 2009. PMID: 20213383 Review.
The incidence rates of childhood and adolescent osteosarcoma with 95% confidence intervals areas follows: Blacks, 6.8/year/million; Hispanics, 6.5/year/million; and Caucasians, 4.6/year/million. ...Cancer deaths due to bone and joint malignant neoplasms represent 8.9% of a …
The incidence rates of childhood and adolescent osteosarcoma with 95% confidence intervals areas follows: Blacks, 6.8/year/million; H …
Small round cell sarcomas.
Cidre-Aranaz F, Watson S, Amatruda JF, Nakamura T, Delattre O, de Alava E, Dirksen U, Grünewald TGP. Cidre-Aranaz F, et al. Nat Rev Dis Primers. 2022 Oct 6;8(1):66. doi: 10.1038/s41572-022-00393-3. Nat Rev Dis Primers. 2022. PMID: 36202860 Review.
SRCSs comprise new entities defined by specific genetic abnormalities, namely EWSR1-non-ETS fusions, CIC-rearrangements or BCOR genetic alterations, as well as EWSR1-ETS fusions in the prototypic SRCS Ewing sarcoma. These gene fusions mainly encode aberrant oncogenic trans …
SRCSs comprise new entities defined by specific genetic abnormalities, namely EWSR1-non-ETS fusions, CIC-rearrangements or BCOR genetic alte …
Kaposi sarcoma.
Cesarman E, Damania B, Krown SE, Martin J, Bower M, Whitby D. Cesarman E, et al. Nat Rev Dis Primers. 2019 Jan 31;5(1):9. doi: 10.1038/s41572-019-0060-9. Nat Rev Dis Primers. 2019. PMID: 30705286 Free PMC article. Review.
Kaposi sarcoma (KS) gained public attention as an AIDS-defining malignancy; its appearance on the skin was a highly stigmatizing sign of HIV infection during the height of the AIDS epidemic. ...Currently, most cases of KS occur in sub-Saharan Africa, where KSHV infection i …
Kaposi sarcoma (KS) gained public attention as an AIDS-defining malignancy; its appearance on the skin was a highly stigmatizing sign …
Sarcomas.
HaDuong JH, Martin AA, Skapek SX, Mascarenhas L. HaDuong JH, et al. Pediatr Clin North Am. 2015 Feb;62(1):179-200. doi: 10.1016/j.pcl.2014.09.012. Pediatr Clin North Am. 2015. PMID: 25435119 Review.
Malignant bone tumors (osteosarcoma, Ewing sarcoma) and soft-tissue sarcomas (rhabdomyosarcoma, nonrhabdomyosarcoma) account for approximately 14% of childhood malignancies. Successful treatment of patients with sarcoma depends on a multidisciplinary approach …
Malignant bone tumors (osteosarcoma, Ewing sarcoma) and soft-tissue sarcomas (rhabdomyosarcoma, nonrhabdomyosarcoma) account for appr …
Chondroblastoma-like Osteosarcoma.
Hmada YA, Bernieh A, Morris RW, Lewin J, Allen T. Hmada YA, et al. Arch Pathol Lab Med. 2020 Jan;144(1):15-17. doi: 10.5858/arpa.2019-0191-RA. Epub 2019 Aug 7. Arch Pathol Lab Med. 2020. PMID: 31389716 Free article. Review.
The tumor is slightly more common in males, with a broad age range (from childhood to elderly). The most commonly involved bones are the metatarsus and tibia, followed by the femur. ...
The tumor is slightly more common in males, with a broad age range (from childhood to elderly). The most commonly involved bones are …
Non-rhabdomyosarcoma soft-tissue sarcoma.
Milgrom SA, Million L, Mandeville H, Safwat A, Ermoian RP, Terezakis S. Milgrom SA, et al. Pediatr Blood Cancer. 2021 May;68 Suppl 2:e28279. doi: 10.1002/pbc.28279. Pediatr Blood Cancer. 2021. PMID: 33818885 Review.
Non-rhabdomyosarcoma soft-tissue sarcomas (NRSTS) comprise 4% of childhood cancers and consist of numerous histologic subtypes. Prognostic factors associated with poor outcome include high histologic grade, large tumor size, presence of metastases, and unresectability. ...
Non-rhabdomyosarcoma soft-tissue sarcomas (NRSTS) comprise 4% of childhood cancers and consist of numerous histologic subtypes. Progn …
Pediatric Sarcomas.
Williams RF, Fernandez-Pineda I, Gosain A. Williams RF, et al. Surg Clin North Am. 2016 Oct;96(5):1107-25. doi: 10.1016/j.suc.2016.05.012. Surg Clin North Am. 2016. PMID: 27542645 Review.
Pediatric sarcomas are a heterogeneous group of tumors accounting for approximately 10% of childhood solid tumors. Treatment is focused on multimodality therapy, which has improved the prognosis over the past two decades. ...The most common bone sarcomas are osteosarcomas …
Pediatric sarcomas are a heterogeneous group of tumors accounting for approximately 10% of childhood solid tumors. Treatment is focus …
652 results