ATRT-21. RHABDOID PREDISPOSITION SYNDROME: REPORT OF MOLECULAR PROFILES AND TREATMENT APPROACH IN THREE CHILDREN WITH SYNCHRONOUS ATYPICAL TERATOID/RHABDOID TUMOR AND MALIGNANT RHABDOID TUMOR

BACKGROUND: Rhabdoid predisposition syndrome is characterized by germline alterations in SMARCB1 or SMARCA4, leading to synchronous or metachronous central nervous system (CNS) and extra-CNS rhabdoid tumors. Rare survivors have been reported to date. METHODS: We describe the molecular profiling and...

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محفوظ في:
التفاصيل البيبلوغرافية
الحاوية / القاعدة:Neuro Oncol
المؤلفون الرئيسيون: Shatara, Margaret, Gupta, Ajay, Arja, Mohamed H Abu, Conley, Suzanne E, Patel, Priyal, Boué, Daniel R, Pierson, Christopher R, Thomas, Diana L, Meyer, Erin K, Shah, Summit H, Jones, Jeremy, Martin, Lisa, McAllister, Aaron, Schieffer, Kathleen M, Varga, Elizabeth A, Leraas, Kristen, Lichtenberg, Tara, LaHaye, Stephanie, Miller, Katherine E, Magrini, Vincent, Wilson, Richard K, Cottrell, Catherine E, Mardis, Elaine R, Aldrink, Jennifer H, Auletta, Jeffery J, Pindrik, Jonathan, Leonard, Jeffrey R, Osorio, Diana S, Finlay, Jonathan L, Ranalli, Mark, AbdelBaki, Mohamed S
التنسيق: Artigo
اللغة:Inglês
منشور في: Oxford University Press 2020
الموضوعات:
Atypical Teratoid/Rhabdoid Tumors
الوصول للمادة أونلاين:https://ncbi.nlm.nih.gov/pmc/articles/PMC7715330/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/noaa222.020
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