Activated growth signaling pathway expression in Ewing sarcoma and clinical outcome
✍ Scribed by Jaume Mora; Eva Rodríguez; Carmen de Torres; Teresa Cardesa; José Ríos; Teresa Hernández; Antonio Cardesa; Enrique de Alava
- Book ID
- 112167954
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 481 KB
- Volume
- 58
- Category
- Article
- ISSN
- 1545-5009
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## Abstract ## BACKGROUND: Ewing sarcoma can arise in either bone or soft tissue. The purpose of this study was to investigate whether patient characteristics, treatment strategies, and outcomes differ between skeletal Ewing sarcoma and extraskeletal Ewing sarcoma (EES). ## METHODS: Patients <40
## Background: Ewing sarcoma is associated with a nonrandom pattern of primary and secondary chromosomal aberrations. whereas the finding of rearrangements of chromosome 22, usually in the form of a balanced translocation t(11;22)(q24;q12), is important diagnostically, nothing is known about the po