TBThomas Benner

Thomas Benner

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Thomas Benner has a total of 22 co-authors. Here are the top co-authors by number of shared publications:


Latest Publications

  • Open Access

    Evaluating effects of normobaric oxygen therapy in acute stroke with MRI-based predictive models

    by Ona Wu, Thomas Benner, Luca Roccatagliata, Mingwang Zhu, Pamela W Schaefer, Alma G Sorensen, Aneesh B Singhal

    Voxel-based algorithms using acute multiparametric-MRI data have been shown to accurately predict tissue outcome after stroke. We explored the potential of MRI-based predictive algorithms to objectively assess the effects of normobaric oxygen therapy (NBO), an investigational stroke treatment, using data from a pilot study of NBO in acute stroke.


  • Open Access

    Diffusion imaging with prospective motion correction and reacquisition

    by Thomas Benner, André J. W. van der Kouwe, A. Gregory Sorensen

    A major source of artifacts in diffusion‐weighted imaging is subject motion. Slow bulk subject motion causes misalignment of data when more than one average or diffusion gradient direction is acquired. Fast bulk subject motion can cause signal dropout artifacts in diffusion‐weighted images and results in erroneous derived maps, e.g., fractional anisotropy maps. To address both types of artifacts, a fully automatic method is presented that combines prospective motion correction with a reacquisition scheme. Motion correction is based on the prospective acquisition correction method modified to work with diffusion‐weighted data. The images to reacquire are determined automatically during the acquisition from the imaging data, i.e., no extra reference scan, navigators, or external devices are necessary. The number of reacquired images, i.e., the additional scan duration can be adjusted freely. Diffusion‐weighted prospective acquisition correction corrects slow bulk motion well and reduces misalignment artifacts like image blurring. Mean absolute residual values for translation and rotation were <0.6 mm and 0.5°. Reacquisition of images affected by signal dropout artifacts results in diffusion maps and fiber tracking free of artifacts. The presented method allows the reduction of two types of common motion related artifacts at the cost of slightly increased acquisition time. Magn Reson Med, 2011.


  • Open Access

    Real-time RF pulse adjustment forB0 drift correction

    by Thomas Benner, André J.W. van der Kouwe, John E. Kirsch, A. Gregory Sorensen


  • Comparison of Manual and Automatic Section Positioning of Brain MR Images

    by Thomas Benner, Jonathan J. Wisco, André J. W. van der Kouwe, Bruce Fischl, Mark G. Vangel, Fred H. Hochberg, A. Gregory Sorensen

    The study protocol was approved by the institutional review board and was in full compliance with HIPAA guidelines. Informed consent was obtained from all patients. The purpose of this study was to prospectively compare intra- and intersubject variability of manual versus automatic magnetic resonance (MR) imaging section prescription. In two examinations, T2-weighted series were acquired with both methods. All intrasubject and three of six intersubject section prescription variances were significantly higher for manual prescription (P < .01). Root mean square errors confirmed better coregistration of the automated approach (P < .001). Automatic section prescription leads to improved reproducibility of imaging orientations for intra- and intersubject series in clinical practice. © RSNA, 2006


  • Cerebral MR perfusion imaging: First clinical application of a 1 M gadolinium chelate (Gadovist 1.0) in a double-blinded randomized dose-finding study

    by Thomas Benner, Peter Reimer, Gunter Erb, Gerhard Schuierer, Sabine Heiland, Carsten Fischer, Viviane Geens, Klaus Sartor, Michael Forsting

    The purpose of this study was to evaluate efficacy and safety of the 1 M gadolinium chelate Gadovist 1.0 for assessment of cerebral hemodynamics with dynamic susceptibility contrast‐enhanced magnetic resonance (MR) imaging. Eighty‐nine patients with carotid artery stenosis or cerebral infarcts were included in this multicenter, double‐blinded study using five dose groups from 0.1 to 0.5 mmol/kg. Imaging was performed with 1‐T scanners using a T2*‐weighted fast low‐angle shot (FLASH) sequence. Dose‐dependent changes in quantitative and qualitative parameters describing signal‐time curves and relative regional cerebral blood volume maps were investigated. For safety evaluation, vital signs, clinical and laboratory tests, and adverse events were assessed. The quantitative measurements revealed an optimal dose of 0.4 mmol/kg. The qualitative evaluation revealed that the required qualitative assessment for clinical purposes was already reached at a dose of 0.3 mmol/kg. No significant changes in vital signs and laboratory tests were found. No serious adverse events were observed. The combined results revealed the dose of 0.3 mmol/kg as the diagnostically adequate dose given the gradient‐echo sequence and field strength used. Gadovist 1.0 has been shown to be a safe and well‐tolerated contrast agent. J. Magn. Reson. Imaging 2000;12:371–380.