Diagnosis and treatment of Ewing sarcoma of the bone: a review article (Q28085071)

Crossref

language of work or name

1 reference

March 2015

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Journal of Orthopaedic Science

1 March 2015

3 references

13 March 2019

3 April 2019

7 August 2019

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13 March 2019

3 April 2019

7 August 2019

20

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issue

2

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page(s)

250-63

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EWS-FLI1 fusion transcript structure is an independent determinant of prognosis in Ewing's sarcoma

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High-dose melphalan, etoposide, total-body irradiation, and autologous stem-cell reconstitution as consolidation therapy for high-risk Ewing's sarcoma does not improve prognosis.

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EWS-FLI1 and EWS-ERG gene fusions are associated with similar clinical phenotypes in Ewing's sarcoma.

27 November 2018

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Extraskeletal neoplasm resembling Ewing's sarcoma

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[Chromosomal translocation (11; 22) in cell lines of Ewing's sarcoma]

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Multimodal therapy for the management of primary, nonmetastatic Ewing's sarcoma of bone: a long-term follow-up of the First Intergroup study

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Morphologic and immunophenotypic diversity in Ewing family tumors: a study of 66 genetically confirmed cases

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The concept of curative margin in surgery for bone and soft tissue sarcoma

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Neuronal and glial markers in tumours of neuroblastic origin

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Fusion of an ETS-family gene, EIAF, to EWS by t(17;22)(q12;q12) chromosome translocation in an undifferentiated sarcoma of infancy

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The non-vascularised fibular graft: a simple and successful method of reconstruction of the pelvic ring after internal hemipelvectomy

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Hip transposition as a limb salvage procedure following the resection of periacetabular tumors

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Genetic imbalances revealed by comparative genomic hybridization in Ewing tumors

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Long-term results in 144 localized Ewing's sarcoma patients treated with combined therapy

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Reconstruction using an autograft containing tumour treated by liquid nitrogen

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Current management of Ewing's sarcoma

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Treatment outcome of pelvic sarcomas in young children: orthopaedic and oncologic analysis

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Pelvic Ewing sarcoma: a retrospective analysis of 241 cases

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Cluster analysis of immunohistochemical profiles in synovial sarcoma, malignant peripheral nerve sheath tumor, and Ewing sarcoma

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12 December 2020

Clinical outcome of patients with Ewing sarcoma family of tumors of bone in Japan: the Japanese Musculoskeletal Oncology Group cooperative study

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12 December 2020

Multimodal therapy for the management of nonpelvic, localized Ewing's sarcoma of bone: intergroup study IESS-II

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12 December 2020

The neuroectodermal tumor of bone

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12 December 2020

Rarity of Ewing's sarcoma in China

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Significance of surgical margin on the prognosis of patients with Ewing's sarcoma. A report from the Cooperative Ewing's Sarcoma Study

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12 December 2020

MIC2 is a specific marker for ewing's sarcoma and peripheral primitive neuroectodermal tumors. Evidence for a common histogenesis of ewing's sarcoma and peripheral primitive neuroectodermal tumors from MIC2 expression and specific chromosome aberrati

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12 December 2020

10.1007/S00776-014-0687-Z

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DOI

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PubMed publication ID

25691401

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