G
Gereon R. Fink
Researcher at Forschungszentrum Jülich
Publications - 976
Citations - 67974
Gereon R. Fink is an academic researcher from Forschungszentrum Jülich. The author has contributed to research in topics: Medicine & Functional magnetic resonance imaging. The author has an hindex of 114, co-authored 867 publications receiving 60853 citations. Previous affiliations of Gereon R. Fink include University of Geneva & University of Hamburg.
Papers
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Journal ArticleDOI
PET imaging of a butterfly glioblastoma
TL;DR: MET-PET imaging added substantial diagnostic information that strongly suggested the diagnosis of GBM and helped to delineate the tumor extension in a 37-year-old woman with a “butterfly” GBM.
Journal ArticleDOI
Evaluation of FET PET Radiomics Feature Repeatability in Glioma Patients.
Robin Gutsche,Jürgen Scheins,Martin Kocher,Khaled Bousabarah,Gereon R. Fink,Nadim Joni Shah,Karl-Josef Langen,Norbert Galldiks,Philipp Lohmann +8 more
TL;DR: In this paper, a test-retest analysis based on equivalent but statistically independent subsamples of FET PET images was performed in 50 newly diagnosed and histomolecularly characterized glioma patients, where a total of 1,302 radiomics features were calculated from semi-automatically segmented tumor volumes-of-interest (VOIs) and spherical VOIs were positioned in the tumor and healthy brain tissue.
Journal ArticleDOI
Räumlicher Neglect
Gereon R. Fink,W. Heide +1 more
TL;DR: In this article, Hemi-Neglect wird am haufigsten nach rechtshemispharischen Lasionen, insbesondere des rechten inferioren Parietalkortex and des recht temporoparietalen Ubergangskortex beobachtet.
Journal ArticleDOI
Selecting the Most Effective DBS Contact in Essential Tremor Patients Based on Individual Tractography.
Jan Niklas Petry-Schmelzer,Till A. Dembek,Julia K. Steffen,Hannah Jergas,Haidar S. Dafsari,Gereon R. Fink,Gereon R. Fink,Veerle Visser-Vandewalle,Michael T. Barbe +8 more
TL;DR: In this paper, the authors investigated whether the most effective DBS contact could be determined from calculating stimulation overlap with the individual dentatorubrothalamic tract (DRTT), and found that the DRTT overlap explained 26.7% of the variance in the clinical outcomes (p < 0.001).
Long term history of a congenital core-rod myopathy with compound heterozygous mutations in the Nebulin gene.
Gilbert Wunderlich,Anna Brunn,Hülya-Sevcan Daimagüler,Tarik Bozoglu,Gereon R. Fink,Helmar C. Lehmann,Joachim Weis,Sebahattin Cirak +7 more
TL;DR: A 54-year-old female with a rare histological myopathy presentation of co-occurring cores and rods and even a scoliosis surgery at the age of 18 years has failed to initiate a neurological workup.