Abstract
This chapter delves into the molecular and genomic mechanisms underlying a diverse spectrum of CNS tumors. Specifically, the chapter covers gliomas, ependymomas, medulloblastomas, atypical teratoid/rhabdoid tumors, pineal region tumors, meningiomas, CNS solitary fibrous tumors/hemangiopericytomas, hemangioblastomas, vestibular schwannomas, and craniopharyngiomas. Through a series of multiple-choice questions, this chapter facilitates a deeper understanding of the molecular and genomic foundations of CNS tumors and further explores the clinical characteristics of specific molecular subtypes of these tumors.
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Atallah, O. et al. (2024). Tumors Molecular and Genomic Mechanism and Diagnostics of CNS Tumors. In: Hoz, S.S., et al. Surgical Neuro-Oncology. Springer, Cham. https://doi.org/10.1007/978-3-031-53642-7_2
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DOI: https://doi.org/10.1007/978-3-031-53642-7_2
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