.png){kind=icon}
.png){kind=icon}
Return
Ewing's Sarcoma
.png){kind=icon}
OA
AI
DOI：10.1056/NEJMra2028910.png)
.png){kind=icon}
Original request for help.png){kind=icon}
Share.png){kind=icon}
Save
Abstract
En 中文
Ewing's sarcoma, an aggressive cancer of bone and soft tissue, primarily affects children and young adults. A t(11;22) translocation is noted in 85 to 90% of cases. Management includes surgery, radiotherapy, and chemotherapy. The 5-year survival is about 70%.
Keywords:
FACTOR-I RECEPTOR
TRANSCRIPTION FACTOR
MONOCLONAL-ANTIBODY
PROGNOSTIC-FACTORS
GENOMIC LANDSCAPE
PROTEIN EWS-FLI1
GENE FUSION
TUMORS
GROWTH
EWS
Journal
IF:
78.5
Papers:
2.7W
Citations:
39.7W