Molecular characterization of CNS paragangliomas identifies cauda equina paragangliomas as a distinct tumor entity

Paragangliomas/pheochromocytomas are rare neuroendocrine tumors that arise from the adrenal gland or ganglia at various sites throughout the body. They display a remarkable diversity of driver alterations and are associated with germline mutations in up to 40% of the cases. Comprehensive molecular p...

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Detalhes bibliográficos
Publicado no:Acta Neuropathol
Main Authors: Schweizer, Leonille, Thierfelder, Felix, Thomas, Christian, Soschinski, Patrick, Suwala, Abigail, Stichel, Damian, Wefers, Annika K., Wessels, Lars, Misch, Martin, Kim, Hee-yeong, Jödicke, Ruben, Teichmann, Daniel, Kaul, David, Kahn, Johannes, Bockmayr, Michael, Hasselblatt, Martin, Younsi, Alexander, Unterberg, Andreas, Knie, Bettina, Walter, Jan, Al Safatli, Diaa, May, Sven-Axel, Jödicke, Andreas, Ntoulias, Georgios, Moskopp, Dag, Vajkoczy, Peter, Heppner, Frank L., Capper, David, Hartmann, Wolfgang, Hartmann, Christian, von Deimling, Andreas, Reuss, David E., Schöler, Anne, Koch, Arend
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Berlin Heidelberg 2020
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Original Paper
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7666289/
https://ncbi.nlm.nih.gov/pubmed/32926213
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00401-020-02218-7
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