% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{ElAyadi:143310,
author = {M. El-Ayadi and M. Ansari and C. D. Kühnöl and A. Bendel
and D. Sturm$^*$ and T. Pietsch and C. M. Kramm and A. O.
von Bueren},
title = {{O}ccurrence of high-grade glioma in {N}oonan syndrome:
{R}eport of two cases.},
journal = {Pediatric blood $\&$ cancer},
volume = {66},
number = {5},
issn = {1545-5017},
address = {New York, NY},
publisher = {Wiley},
reportid = {DKFZ-2019-00900},
pages = {e27625},
year = {2019},
abstract = {Noonan syndrome (NS) is an autosomal dominant disorder
commonly caused by PTPN11 germline mutations. Patients are
characterized by short stature, congenital heart defects,
facial dysmorphism, and increased risk of malignancies
including brain tumors. Commonly associated brain tumors are
dysembryoplastic neuroepithelial tumor and low-grade glioma.
We report two cases of anaplastic astrocytoma with
PTPN11-related NS. We conducted a systematic search of
medical databases looking for other reported cases of
high-grade glioma associated with NS and identified 24 cases
of brain tumors, all of which were low-grade glial or
glioneuronal tumors except for one case of medulloblastoma.},
cin = {B062},
ddc = {610},
cid = {I:(DE-He78)B062-20160331},
pnm = {312 - Functional and structural genomics (POF3-312)},
pid = {G:(DE-HGF)POF3-312},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:30693642},
doi = {10.1002/pbc.27625},
url = {https://inrepo02.dkfz.de/record/143310},
}