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@ARTICLE{Gerstner:132713,
author = {E. R. Gerstner and K. Pajtler$^*$},
title = {{E}pendymoma.},
journal = {Seminars in neurology},
volume = {38},
number = {1},
issn = {1098-9021},
address = {New York, NY},
publisher = {Thieme Medical Publ.},
reportid = {DKFZ-2018-00367},
pages = {104 - 111},
year = {2018},
abstract = {Ependymoma can arise throughout the whole neuraxis. In
children, tumors predominantly occur intracranially, whereas
the spine is the most prevalent location in adults.
Significant variance in the grade II versus grade III
distinction of ependymomas has led to the acknowledgment
that the clinical utility of histopathological
classification is limited. Epigenomic profiling efforts have
identified molecularly distinct groups of ependymomas that
adequately reflect the biological, clinical, and
histopathological heterogeneities across anatomical
compartments, age groups, and grades. The recent update of
the World Health Organization classification of central
nervous system tumors has already integrated one of these
groups, and molecular classification will be part of future
clinical trials to improve risk stratification. Clinical
management of this rare disease is challenging, making
professional experience and intensified multidisciplinary
cooperation pivotal factors for treatment success. Novel
research strategies are currently applied for target
discovery in ependymomas since for most molecular groups,
genetic drivers are unknown.},
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:29548057},
doi = {10.1055/s-0038-1636503},
url = {https://inrepo02.dkfz.de/record/132713},
}