EMBR-17. PINEOBLASTOMA SEGREGATES INTO MOLECULAR SUBTYPES WITH DISTINCT CLINICOPATHOLOGIC FEATURES: REPORT FROM THE RARE BRAIN TUMOR CONSORTIUM

Pineoblastoma (PB) is a rare but aggressive pediatric brain tumour arising from the pineal gland. Outcomes remain dismal with long-term survival rates between 10–40% despite intensive treatment regimens. Although germline RB1 and DICER1 alterations have been reported in a small proportion of PB, the...

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Publicado no:Neuro Oncol
Main Authors: Li, Bryan, Vasiljevic, Alexandre, Ho, Ben, Norman, Joseph, Lu, Mei, Hwang, Eugene, Hansford, Jordan, Jouvet, Anne, Laquerriere, Annie, Delisle, Marie-Bernadette, Gururangan, Sridharan, Fangusaro, Jason, Forest, Fabien, Sumihito, Nobusawa, Toledano, Helen, Birks, Diane, Fan, Xing, Fouladi, Maryam, Gajjar, Amar, Gauchotte, Guillaume, Hoffman, Lindsey, Jones, Chris, Loussouarn, Delphine, Mokhtari, Karima, Pomeroy, Scott, Rousseau, Audrey, Somers, Gino, Taylor, Michael, Ziegler, David, Hawkins, Cynthia, Bouffet, Eric, Grundy, Richard, Dufour, Christelle, Huang, Annie
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2018
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6012224/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/noy059.201
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