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Pediatric Blood & Cancer|December 4, 2019
Indolent course of brainstem tumors with K27M-H3.3 mutationLorena V Baroni, Palma Solano-Paez, Liana Nobre, et al.Neuro-Oncology Practice|August 9, 2020
Bevacizumab for pediatric radiation necrosisLorena V Baroni, Daniel Alderete, Palma Solano-Paez, et al.The Lancet. Child & Adolescent Health|October 2, 2021
Clinical phenotypes and prognostic features of embryonal tumours with multi-layered rosettes: a Rare Brain Tumor Registry studySara Khan, Palma Solano-Paez, Tannu Suwal, et al.Cancer Medicine|May 27, 2016
Improved 6-year overall survival in AT/RT - results of the registry study Rhabdoid 2007Kerstin Bartelheim, Karolina Nemes, Angela Seeringer, et al.Neuro-Oncology|December 29, 2019
Age and DNA methylation subgroup as potential independent risk factors for treatment stratification in children with atypical teratoid/rhabdoid tumorsMichael C Frühwald, Martin Hasselblatt, Karolina Nemes, et al.Acta Neuropathologica|December 11, 2019
Pineoblastoma segregates into molecular sub-groups with distinct clinico-pathologic features: a Rare Brain Tumor Consortium registry studyBryan K Li, Alexandre Vasiljevic, Christelle Dufour, et al.Cancer Cell|July 10, 2019
A C19MC-LIN28A-MYCN Oncogenic Circuit Driven by Hijacked Super-enhancers Is a Distinct Therapeutic Vulnerability in ETMRs: A Lethal Brain TumorPatrick Sin-Chan, Iqra Mumal, Tannu Suwal, et al.Pageof 1