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Dive into the research topics where Uwe Klose is active.

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Featured researches published by Uwe Klose.


Journal of Cognitive Neuroscience | 1999

Activation of Cortical and Cerebellar Motor Areas during Executed and Imagined Hand Movements: An fMRI Study

Martin Lotze; Pedro Montoya; Michael Erb; Ernst Hülsmann; Herta Flor; Uwe Klose; Niels Birbaumer; Wolfgang Grodd

Brain activation during executed (EM) and imagined movements (IM) of the right and left hand was studied in 10 healthy right-handed subjects using functional magnetic resonance imagining (fMRI). Low electromyographic (EMG) activity of the musculi flexor digitorum superficialis and high vividness of the imagined movements were trained prior to image acquisition. Regional cerebral activation was measured by fMRI during EM and IM and compared to resting conditions. Anatomically selected regions of interest (ROIs) were marked interactively over the entire brain. In each ROI activated pixels above a t value of 2.45 (p < 0.01) were counted and analyzed. In all subjects the supplementary motor area (SMA), the premotor cortex (PMC), and the primary motor cortex (M1) showed significant activation during both EM and IM; the somatosensory cortex (S1) was significantly activated only during EM. Ipsilateral cerebellar activation was decreased during IM compared to EM. In the cerebellum, IM and EM differed in their foci of maximal activation: Highest ipsilateral activation of the cerebellum was observed in the anterior lobe (Larsell lobule H IV) during EM, whereas a lower maximum was found about 2-cm dorsolateral (Larsell lobule H VII) during IM. The prefrontal and parietal regions revealed no significant changes during both conditions. The results of cortical activity support the hypothesis that motor imagery and motor performance possess similar neural substrates. The differential activation in the cerebellum during EM and IM is in accordance with the assumption that the posterior cerebellum is involved in the inhibition of movement execution during imagination.


Neuroreport | 1998

fMRI reveals amygdala activation to human faces in social phobics.

Niels Birbaumer; Wolfgang Grodd; Oliver Diedrich; Uwe Klose; Michael Erb; Martin Lotze; Frank Schneider; Ute Weiss; Herta Flor

FUNCTIONAL magnetic resonance imaging was used to determine the activation of the amygdala while seven social phobics and five healthy controls were exposed to slides of neutral faces as well as aversive odor stimuli. The amygdala was selectively activated in the social phobics during presentation of the face stimuli. The data show for the first time that the amygdala is active in human phobics when they are exposed to potentially fear-relevant stimuli. Further research is needed to determine the extent to which overactivation of the amygdala precedes or is a consequence of phobia.


Psychiatry Research-neuroimaging | 1997

Functional MRI reveals left amygdala activation during emotion

Frank Schneider; Wolfgang Grodd; Ute Weiss; Uwe Klose; Katharina R Mayer; Thomas Nägele; Ruben C. Gur

The potential of functional magnetic resonance imaging (fMRI) for experimental studies of the brain and behavior considerable given its superior time and spatial resolution, but few studies have attempted to validate them against established methods for measuring cerebral activation. In a previous study absolute regional cerebral blood flow was measured in 16 healthy individuals using quantitative H215O-PET during standardized happy and sad mood induction and during two non-emotional control conditions. During sad mood, blood flow increased in the left amygdala and these changes correlated with shifts towards a negative affect. In the present study blood oxygenation level dependent (BOLD) changes were measured with fMRI during the same experimentally controlled mood states and control tasks. Twelve right-handed normal subjects were examined with a T2*-weighted FLASH sequence. A significant increase in signal intensity was found during sad as well as happy mood induction in the left amygdala. This converging evidence supports the potential of fMRI for advancing the understanding of neural substrates for emotional experience in humans.


Magnetic Resonance in Medicine | 2004

FAIR True-FISP perfusion imaging of the kidneys

Petros Martirosian; Uwe Klose; Irina Mader; Fritz Schick

Most arterial spin labeling (ASL) techniques apply echoplanar imaging (EPI) because this strategy provides relatively high SNR in short measuring times. Unfortunately, those techniques are very susceptible to static magnetic field inhomogeneities and perfusion signals from organs with fast transverse relaxation might decrease due to the exchange of water molecules in capillaries and organ tissue combined with relatively long echo times of EPI sequences. To overcome these problems a novel imaging technique, FAIR True‐FISP, was developed. It combines a FAIR (flow‐sensitive alternating inversion recovery) perfusion preparation and a true fast imaging with steady precession (True‐FISP) data acquisition strategy. True‐FISP was chosen since this sequence type does not show the mentioned disadvantages of EPI, but provides a similar SNR per measuring time. An important problem of this approach is that True‐FISP sequences usually work in a steady state which is independent of a previous preparation of magnetization. For this reason a sequence structure had to be developed which keeps the advantages of True‐FISP and makes the signal intensity sensitive to the FAIR preparation. Breathhold and nonbreathhold examinations of kidneys are presented and possible strategies to quantitative flow measurements are reported. It is shown that correction of spatially inhomogeneous receiver coil characteristics is easily feasible and leads to clinically valuable perfusion examinations of kidneys without application of potentially nephrotoxic contrast media. Magn Reson Med 51:353–361, 2004.


Magnetic Resonance in Medicine | 2003

Comparison of longitudinal metabolite relaxation times in different regions of the human brain at 1.5 and 3 Tesla

Thomas Ethofer; Irina Mader; Uwe Seeger; Gunther Helms; Michael Erb; Wolfgang Grodd; Albert C. Ludolph; Uwe Klose

In vivo longitudinal relaxation times of N‐acetyl compounds (NA), choline‐containing substances (Cho), creatine (Cr), myo‐inositol (mI), and tissue water were measured at 1.5 and 3 T using a point‐resolved spectroscopy (PRESS) sequence with short echo time (TE). T1 values were determined in six different brain regions: the occipital gray matter (GM), occipital white matter (WM), motor cortex, frontoparietal WM, thalamus, and cerebellum. The T1 relaxation times of water protons were 26–38% longer at 3 T than at 1.5 T. Significantly longer metabolite T1 values at 3 T (11–36%) were found for NA, Cho, and Cr in the motor cortex, frontoparietal WM, and thalamus. The amounts of GM, WM, and cerebrospinal fluid (CSF) within the voxel were determined by segmentation of a 3D image data set. No influence of tissue composition on metabolite T1 values was found, while the longitudinal relaxation times of water protons were strongly correlated with the relative GM content. Magn Reson Med 50:1296–1301, 2003.


Magnetic Resonance in Medicine | 2003

Parameterized evaluation of macromolecules and lipids in proton MR spectroscopy of brain diseases

Uwe Seeger; Uwe Klose; Irina Mader; Wolfgang Grodd; Thomas Nägele

Short echo time (TE) proton MR spectra of the brain include signals of several metabolites as well as macromolecules. In various pathologies, such as brain tumors and multiple sclerosis (MS), the presence of mobile lipids or pathologically altered macromolecules may provide useful additional diagnostic information. A reliable quantitation of these resonances, however, is often not possible due to the lack of adequate prior knowledge. Furthermore, even if advanced fitting procedures are used, a reliable evaluation of metabolites in the presence of pathological lipids or macromolecules often fails if the latter are omitted in the spectral evaluation. In this study, a method is presented for the simultaneous evaluation of all visible components, including metabolites, lipids, and macromolecules, by the use of the fitting procedure LCModel. A standard basis set of brain metabolites was extended by inclusion of parameterized components for macromolecules and lipids that were derived from metabolite‐nulled in vivo spectra of normal brain and high‐grade gliomas, respectively. The improved spectral quantitation is demonstrated in glial brain tumors and MS lesions as well as in normal brain. It is pointed out that both macromolecules and lipids must be included to provide a proper spectral evaluation. Magn Reson Med 49:19–28, 2003.


Brain and Language | 2000

The Concreteness Effect: Evidence for Dual Coding and Context Availability☆

Frank Jessen; Reinhard Heun; Michael Erb; Dirk-Oliver Granath; Uwe Klose; Andreas Papassotiropoulos; Wolfgang Grodd

The term concreteness effect refers to the observation that concrete nouns are processed faster and more accurately than abstract nouns in a variety of cognitive tasks. Two models have been proposed to explain the neuronal basis of the concreteness effect. The dual-coding theory attributes the advantage to the access of a right hemisphere image based system in addition to a verbal system by concrete words. The context availability theory argues that concrete words activate a broader contextual verbal support, which results in faster processing, but do not access a distinct image based system. We used event-related fMRI to detect the brain regions that subserve to the concreteness effect. We found greater activation in the lower right and left parietal lobes, in the left inferior frontal lobe and in the precuneus during encoding of concrete compared to abstract nouns. This makes a single exclusive theory unlikely and rather suggests a combination of both models. Superior encoding of concrete words in the present study may result from (1) greater verbal context resources reflected by the activation of left parietal and frontal associative areas, and (2) the additional activation of a non-verbal, perhaps spatial imagery-based system, in the right parietal lobe.


Neuroradiology | 1992

Cerebrospinal fluid flow

G. Schroth; Uwe Klose

SummaryCardiac-related motion of the cerebrospinal fluid (CSF) was investigated by analysis of the velocity-dependent phase of CSF protons and flow-dependent signal enhancement in magnitude images using ECG-gated FLASH sequences. In the cerebral aqueduct, CSF flow from the third to the fourth ventricle begins 200 msafter the R-wave of the ECG and simulates an arterial pulse wave pattern. It lasts about 60% of the cardiac cycle and is followed by backflow from the fourth to the third ventricle, which is slower and shorter. In the spinal canal, oscillating caudad motion precedes flow from the third to the fourth ventricle by about 50–100 ms and issuperimposed on a bulk flow, which moves simultaneously in opposite directions in separate subarachnoid channels; it is directed mainly caudally in the anterior cervical subarachnoid space.


Neuroradiology | 1988

Reversible brain shrinkage in abstinent alcoholics, measured by MRI.

G. Schroth; T. Naegele; Uwe Klose; Karl Mann; Dirk Petersen

SummaryMagnetic resonance imaging of the intracranial CSF volume was compared before and after 5 weeks of confirmed abstinence in 9 alcohol-dependent patients. All patients showed a highly significant reduction in CSF volume in accordance with reexpansion of the brain after alcohol abstinence. T2 values for white matter, estimated by linear regression from 16 echoes of a CPGM sequence, however, showed no significant increase such as occurs in rehydration. This indicates, that alcohol-induced reversible brain atrophy cannot be attributed to fluctuation of free water in the brain only.


NeuroImage | 2005

Single-shot compensation of image distortions and BOLD contrast optimization using multi-echo EPI for real-time fMRI

Nikolaus Weiskopf; Uwe Klose; Niels Birbaumer; Klaus Mathiak

Functional magnetic resonance imaging (fMRI) is most commonly based on echo-planar imaging (EPI). With higher field strengths, gradient performance, and computational power, real-time fMRI has become feasible; that is, brain activation can be monitored during the ongoing scan. However, EPI suffers from geometric distortions due to inhomogeneities of the magnetic field, especially close to air-tissue interfaces. Thus, functional activations might be mislocalized and assigned to the wrong anatomical structures. Several techniques have been reported which reduce geometric distortions, for example, mapping of the static magnetic field B(0) or the point spread function for all voxels. Yet these techniques require additional reference scans and in some cases extensive computational time. Moreover, only static field inhomogeneities can be corrected, because the correction is based on a static reference scan. We present an approach which allows for simultaneous acquisition and distortion correction of a functional image without a reference scan. The technique is based on a modified multi-echo EPI data acquisition scheme using a phase-encoding (PE) gradient with alternating polarity. The images exhibit opposite distortions due to the inverted PE gradient. After adjusting the contrast of the images acquired at different echo times, this information is used for the distortion correction. We present the theory, implementation, and applications of this single-shot distortion correction. Significant reduction in geometric distortion is shown both for phantom images and human fMRI data. Moreover, sensitivity to the blood oxygen level-dependent (BOLD) effect is increased by weighted summation of the undistorted images.

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Uwe Seeger

University of Tübingen

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Fritz Schick

University of Tübingen

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Irina Mader

University of Freiburg

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Sotirios Bisdas

University College London

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