Benjamin Bender
Benjamin Bender
Attending Neuroradiologist, University Hospital Tübingen
Verified email at
Cited by
Cited by
Age-specific CT and MRI templates for spatial normalization
C Rorden, L Bonilha, J Fridriksson, B Bender, HO Karnath
Neuroimage 61 (4), 957-965, 2012
Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study
CD Whelan, A Altmann, JA Botía, N Jahanshad, DP Hibar, J Absil, ...
Brain 141 (2), 391-408, 2018
Nigral stimulation for resistant axial motor impairment in Parkinson’s disease? A randomized controlled trial
D Weiss, M Walach, C Meisner, M Fritz, M Scholten, S Breit, C Plewnia, ...
Brain 136 (7), 2098-2108, 2013
Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum
M Synofzik, AS Soehn, J Gburek-Augustat, J Schicks, KN Karle, R Schüle, ...
Orphanet journal of rare diseases 8 (1), 41, 2013
Iterative reconstruction in head CT: image quality of routine and low-dose protocols in comparison with standard filtered back-projection
A Korn, M Fenchel, B Bender, S Danz, TK Hauser, D Ketelsen, T Flohr, ...
American journal of neuroradiology 33 (2), 218-224, 2012
Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study
EL van der Ende, LH Meeter, JM Poos, JL Panman, LC Jiskoot, ...
The Lancet Neurology 18 (12), 1103-1111, 2019
White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study
SN Hatton, KH Huynh, L Bonilha, E Abela, S Alhusaini, A Altmann, ...
Brain 143 (8), 2454-2473, 2020
The in vivo influence of white matter fiber orientation towards B0 on T2* in the human brain
B Bender, U Klose
NMR in Biomedicine 23 (9), 1071-1076, 2010
Distribution and prognostic relevance of tumor-infiltrating lymphocytes (TILs) and PD-1/PD-L1 immune checkpoints in human brain metastases
PN Harter, S Bernatz, A Scholz, PS Zeiner, J Zinke, M Kiyose, S Blasel, ...
Oncotarget 6 (38), 40836, 2015
In vivo molecular profiling of human glioma using diffusion kurtosis imaging
JM Hempel, S Bisdas, J Schittenhelm, C Brendle, B Bender, H Wassmann, ...
Journal of neuro-oncology 131, 93-101, 2017
Outcome after whole brain radiotherapy alone in intracranial leptomeningeal carcinomatosis from solid tumors
C Gani, AC Müller, F Eckert, C Schroeder, B Bender, G Pantazis, ...
Strahlentherapie und Onkologie 188 (2), 148, 2012
3D gradient echo snapshot CEST MRI with low power saturation for human studies at 3T
A Deshmane, M Zaiss, T Lindig, K Herz, M Schuppert, C Gandhi, ...
Magnetic resonance in medicine 81 (4), 2412-2423, 2019
PI3K Pathway Inhibition Achieves Potent Antitumor Activity in Melanoma Brain Metastases In Vitro and In Vivo
H Niessner, J Schmitz, G Tabatabai, AM Schmid, C Calaminus, ...
Clinical Cancer Research 22 (23), 5818-5828, 2016
Mutation screen reveals novel variants and expands the phenotypes associated with DYNC1H1
AV Strickland, M Schabhüttl, H Offenbacher, M Synofzik, NS Hauser, ...
Journal of neurology 262, 2124-2134, 2015
De novo mutations in hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS)
KN Karle, S Biskup, R Schüle, KJ Schweitzer, R Krüger, P Bauer, ...
Neurology 81 (23), 2039-2044, 2013
Metabolic mapping of gliomas using hybrid MR-PET imaging: feasibility of the method and spatial distribution of metabolic changes
S Bisdas, R Ritz, B Bender, C Braun, C Pfannenberg, M Reimold, ...
Investigative radiology 48 (5), 295-301, 2013
Glioma Grading and Determination of IDH Mutation Status and ATRX loss by DCE and ASL Perfusion
C Brendle, JM Hempel, J Schittenhelm, M Skardelly, G Tabatabai, ...
Clinical Neuroradiology 28, 421-428, 2018
DeepCEST 3T: Robust MRI parameter determination and uncertainty quantification with neural networks—application to CEST imaging of the human brain at 3T
F Glang, A Deshmane, S Prokudin, F Martin, K Herz, T Lindig, B Bender, ...
Magnetic resonance in medicine 84 (1), 450-466, 2020
Motor protein mutations cause a new form of hereditary spastic paraplegia
A Caballero Oteyza, E Battaloğlu, L Ocek, T Lindig, J Reichbauer, ...
Neurology 82 (22), 2007-2016, 2014
STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: evidence from four novel mutations
SN Hayer, T Deconinck, B Bender, K Smets, S Züchner, S Reich, L Schöls, ...
Orphanet journal of rare diseases 12, 1-8, 2017
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