Rhabdoid Tumors
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-030-74448-9_3
Reference124 articles.
1. Tomlinson, G. E., Breslow, N. E., Dome, J., et al. (2005). Rhabdoid tumor of the kidney in the National Wilms' tumor study: Age at diagnosis as a prognostic factor. Journal of Clinical Oncology, 23, 7641–7645.
2. Rorke, L. B., Packer, R. J., & Biegel, J. A. (1996). Central nervous system atypical Teratoid/Rhabdoid tumors of infancy and childhood: Definition of an entity. Journal of Neurosurgery, 85, 56–65.
3. Hilden, J. M., Meerbaum, S., Burger, P., et al. (2004). Central nervous system atypical Teratoid/Rhabdoid tumor: Results of therapy in children enrolled in a registry. Journal of Clinical Oncology, 22, 2877–2884.
4. Tekautz, T. M., Fuller, C. E., Blaney, S., et al. (2005). Atypical Teratoid/Rhabdoid tumors (ATRT): Improved survival in children 3 years of age and older with radiation therapy and high-dose Alkylator-based chemotherapy. Journal of Clinical Oncology, 23, 1491–1499.
5. Geller, J. I., Roth, J. J., & Biegel, J. A. (2015). Biology and treatment of rhabdoid tumor. Critical Reviews in Oncogenesis, 20(3-4), 199–216. https://doi.org/10.1615/critrevoncog.2015013566
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