Treatment of Rhabdomyosarcoma
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-030-51160-9_5
Reference47 articles.
1. Agaram NP, Chen CL, Zhang L, LaQuaglia MP, Wexler L, Antonescu CR (2014) RecurrentMYOD1mutations in pediatric and adult sclerosing and spindle cell rhabdomyosarcomas: evidence for a common pathogenesis. Genes Chromosomes Cancer 53(9):779–787
2. Agaram NP, LaQuaglia MP, Alaggio R, Zhang L, Fujisawa Y, Ladanyi M, Wexler LH, Antonescu CR (2019) MYOD1-mutant spindle cell and sclerosing rhabdomyosarcoma: an aggressive subtype irrespective of age. A reappraisal for molecular classification and risk stratification. Mod Pathol 32(1):27–36. https://doi.org/10.1038/s41379-018-0120-9 . Epub 2018 Sep 4
3. Arndt CA, Bisogno G, Koscielniak E (2018) Fifty years of rhabdomyosarcoma studies on both sides of the pond and lessons learned. Cancer Treatment Rev 68:94–101
4. Arnold MA, Anderson JR, Gastier-Foster JM et al (2016) Histology, fusion status, and outcome in alveolar rhabdomyosarcoma with low-risk clinical features: a report from the Children’s Oncology Group. Pediatr Blood Cancer 63(4):634–639. https://doi.org/10.1002/pbc.25862
5. Bisogno G, Ferrari A, Prete A, Messina C, Basso E, Cecchetto G et al (2009) Sequential high-dose chemotherapy for children with metastatic rhabdomyosarcoma. Eur J Cancer 45:3035–3041
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