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
Differentiation of a Falcine Meningioma From Cerebral Venous Sinus Thrombosis Using DOTATATE PET.
Isabelle Stetter,Jan-Michael Werner,Michael Schroeter,Claudia Baumann,J. Neuneier,Marc Schlamann,Matthias Schmidt,Alexander Drzezga,Gereon R. Fink,Norbert Galldiks +9 more
TL;DR: In this article , the authors presented the case of a 23-year-old woman in whom an MRI suggested a cerebral venous sinus thrombosis and additional atypical MRI findings raised doubts regarding the initial diagnosis.
Book ChapterDOI
Motorik und Handlung
TL;DR: In this article, aufklarung der Prozesse der Bewegungsentstehung is used as a wichtiger Schritt, sich wissenschaftlich-philosophischen Fragen uber die menschliche Fahigkeit der ''willkurlichen Entscheidung (''freier Wille«), der Handlungsabsicht (''Motivation '') sowie des vorausschauenden Planens and Handelns zu nahern.
Journal ArticleDOI
Low beta-band suppression as a tool for DBS contact selection for akinetic-rigid symptoms in Parkinson's disease.
J. Strelow,Till A. Dembek,Juan Carlos Baldermann,Pablo Andrade,Gereon R. Fink,Veerle Visser-Vandewalle,Michael T. Barbe +6 more
TL;DR: In this paper , the utility of low beta-band suppression as a tool for contact selection in subthalamic deep brain stimulation (STN-DBS) for Parkinson's disease (PD) was evaluated.
Journal ArticleDOI
Immuntherapie und zielgerichtete Therapie von Gliomen
Journal ArticleDOI
P 42 Congenital myasthenia in adult patients – a diagnostic and therapeutic challenge
Christian Ritter,S. Cirak,A. Abicht,Helmar C. Lehmann,Anna Brunn,Gereon R. Fink,Michael Schroeter,Gilbert Wunderlich +7 more
TL;DR: Two patients who were first diagnosed CMS in early adulthood show that the diagnosis CMS may be challenging as clinical and diagnostic results may mimic primary myopathy or dystrophic muscle disease as well as mitochondriopathy.