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@ARTICLE{Bozzai:119223,
      author       = {B. Bozzai and M. Hasselblatt and E. Turányi and M. C.
                      Frühwald and R. Siebert and S. Bens and R. Schneppenheim
                      and M. Kool$^*$ and G. Stelczer and T. Hortobágyi and P.
                      Hauser},
      title        = {{A}typical teratoid/rhabdoid tumor arising in a malignant
                      glioma.2},
      journal      = {Pediatric blood $\&$ cancer},
      volume       = {64},
      number       = {1},
      issn         = {1545-5009},
      address      = {New York, NY},
      publisher    = {Wiley},
      reportid     = {DKFZ-2017-00013},
      pages        = {96 - 99},
      year         = {2017},
      abstract     = {Atypical teratoid/rhabdoid tumor (AT/RT), a highly
                      malignant brain tumor in young children, usually arises de
                      novo and has only rarely been described as a secondary
                      malignancy. Here, we present a case of a child with
                      glioblastoma, who was treated postoperatively by a
                      combination of temozolomide, irradiation, and bevacizumab.
                      AT/RT was diagnosed as a secondary tumor, 2.5 years
                      following primary diagnosis. The child died 13 months after
                      the diagnosis of AT/RT. This case demonstrates that
                      malignant gliomas may give rise to AT/RT. It also emphasizes
                      the diagnostic value of a repeated tumor biopsy in the
                      recurrence setting.},
      cin          = {B062 / L101},
      ddc          = {610},
      cid          = {I:(DE-He78)B062-20160331 / I:(DE-He78)L101-20160331},
      pnm          = {312 - Functional and structural genomics (POF3-312)},
      pid          = {G:(DE-HGF)POF3-312},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {pmid:27472468},
      doi          = {10.1002/pbc.26173},
      url          = {https://inrepo02.dkfz.de/record/119223},
}