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@ARTICLE{Northcott:143453,
author = {P. A. Northcott and G. W. Robinson and C. P. Kratz and D.
J. Mabbott and S. L. Pomeroy and S. C. Clifford and S.
Rutkowski and D. W. Ellison and D. Malkin and M. D. Taylor
and A. Gajjar and S. Pfister$^*$},
title = {{M}edulloblastoma.},
journal = {Nature reviews / Disease Primers Disease Primers [...]},
volume = {5},
number = {1},
issn = {2056-676X},
address = {Basingstoke},
publisher = {Nature Publishing Group},
reportid = {DKFZ-2019-01041},
pages = {11},
year = {2019},
abstract = {Medulloblastoma (MB) comprises a biologically heterogeneous
group of embryonal tumours of the cerebellum. Four subgroups
of MB have been described (WNT, sonic hedgehog (SHH), Group
3 and Group 4), each of which is associated with different
genetic alterations, age at onset and prognosis. These
subgroups have broadly been incorporated into the WHO
classification of central nervous system tumours but still
need to be accounted for to appropriately tailor disease
risk to therapy intensity and to target therapy to disease
biology. In this Primer, the epidemiology (including MB
predisposition), molecular pathogenesis and integrative
diagnosis taking histomorphology, molecular genetics and
imaging into account are reviewed. In addition, management
strategies, which encompass surgical resection of the
tumour, cranio-spinal irradiation and chemotherapy, are
discussed, together with the possibility of focusing more on
disease biology and robust molecularly driven patient
stratification in future clinical trials.},
subtyp = {Review Article},
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:30765705},
doi = {10.1038/s41572-019-0063-6},
url = {https://inrepo02.dkfz.de/record/143453},
}