<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns="http://purl.org/rss/1.0/"><channel rdf:about="http://www.mrijournal.com//inpress?rss=yes"><title>Magnetic Resonance Imaging - Articles in Press</title><description>Magnetic Resonance Imaging RSS feed: Articles in Press. 
 MAGNETIC RESONANCE IMAGING (MRI)  is the first international multidisciplinary journal encompassing physical, life, and clinical 
science investigations as they relate to the development and use of magnetic resonance imaging.   MRI  is dedicated to both basic 
research and medical applications, providing a single forum for communication among radiologists, physicists, chemists, biochemists, 
biologists, engineers, internists, pathologists, physiologists, computer scientists, and mathematicians.</description><link>http://www.mrijournal.com//inpress?rss=yes</link><dc:publisher>Elsevier Inc.</dc:publisher><dc:language>en</dc:language><dc:rights> © 2010 Elsevier Inc. All rights reserved. </dc:rights><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:issn>0730-725X</prism:issn><prism:publicationDate>2010-02-22</prism:publicationDate><prism:copyright> © 2010 Elsevier Inc. All rights reserved. </prism:copyright><prism:rightsAgent>healthpermissions@elsevier.com</prism:rightsAgent><items><rdf:Seq><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09003208/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09002951/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09002781/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09003129/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09003191/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09002859/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09002914/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09002999/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09003099/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09003154/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09003166/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09003178/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09003002/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X0900304X/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X0900318X/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09002860/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09002872/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09002975/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09003063/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09003075/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09003087/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09003117/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09003130/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09003142/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09002823/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09002902/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09002926/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X0900294X/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09002963/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09003038/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X0900277X/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09002835/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09002847/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09002938/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09002987/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09003014/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09003051/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09003105/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X0900280X/abstract?rss=yes"/><rdf:li rdf:resource="http://www.mrijournal.com/article/PIIS0730725X09002811/abstract?rss=yes"/></rdf:Seq></items></channel><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09003208/abstract?rss=yes"><title>Coupling of neural activity and fMRI-BOLD in the motion area MT - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09003208/abstract?rss=yes</link><description>Abstract: The fMRI-BOLD contrast is widely used to study the neural basis of sensory perception and cognition. This signal, however, reflects neural activity only indirectly, and the detailed mechanisms of neurovascular coupling and the neurophysiological correlates of the BOLD signal remain debated. Here we investigate the coupling of BOLD and electrophysiological signals in the motion area MT of the macaque monkey by simultaneously recording both signals. Our results demonstrate that a prominent neuronal response property of area MT, so-called motion opponency, can be used to induce dissociations of BOLD and neuronal firing. During the presentation of a stimulus optimally driving the local neurons, both field potentials [local field potentials (LFPs)] and spiking activity [multi-unit activity (MUA)] correlated with the BOLD signal. When introducing the motion opponency stimulus, however, correlations of MUA with BOLD were much reduced, and LFPs were a much better predictor of the BOLD signal than MUA. In addition, for a subset of recording sites we found positive BOLD and LFP responses in the presence of decreases in MUA, regardless of the stimulus used. Together, these results demonstrate that correlations between BOLD and MUA are dependent on the particular site and stimulus paradigm, and foster the notion that the fMRI-BOLD signal reflects local dendrosomatic processing and synaptic activity rather than principal neuron spiking responses.</description><dc:title>Coupling of neural activity and fMRI-BOLD in the motion area MT - Corrected Proof</dc:title><dc:creator>Michael T. Lippert, Thomas Steudel, Frank Ohl, Nikos K. Logothetis, Christoph Kayser</dc:creator><dc:identifier>10.1016/j.mri.2009.12.028</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-02-22</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-02-22</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09002951/abstract?rss=yes"><title>Fast volumetric spatial-spectral MR imaging of hyperpolarized 13C-labeled compounds using multiple echo 3D bSSFP - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09002951/abstract?rss=yes</link><description>Abstract: Purpose: The goal of this work was to develop a fast 3D chemical shift imaging technique for the noninvasive measurement of hyperpolarized 13C-labeled substrates and metabolic products at low concentration.Materials and Methods: Multiple echo 3D balanced steady state magnetic resonance imaging (ME-3DbSSFP) was performed in vitro on a syringe containing hyperpolarized [1,3,3-2H3; 1-13C]2-hydroxyethylpropionate (HEP) adjacent to a 13C-enriched acetate phantom, and in vivo on a rat before and after intravenous injection of hyperpolarized HEP at 1.5 T. Chemical shift images of the hyperpolarized HEP were derived from the multiple echo data by Fourier transformation along the echoes on a voxel by voxel basis for each slice of the 3D data set.Results: ME-3DbSSFP imaging was able to provide chemical shift images of hyperpolarized HEP in vitro, and in a rat with isotropic 7-mm spatial resolution, 93 Hz spectral resolution and 16-s temporal resolution for a period greater than 45 s.Conclusion: Multiple echo 3D bSSFP imaging can provide chemical shift images of hyperpolarized 13C-labeled compounds in vivo with relatively high spatial resolution and moderate spectral resolution. The increased signal-to-noise ratio of this 3D technique will enable the detection of hyperpolarized 13C-labeled metabolites at lower concentrations as compared to a 2D technique.</description><dc:title>Fast volumetric spatial-spectral MR imaging of hyperpolarized 13C-labeled compounds using multiple echo 3D bSSFP - Corrected Proof</dc:title><dc:creator>William H. Perman, Pratip Bhattacharya, Jochen Leupold, Alexander P. Lin, Kent C. Harris, Valerie A. Norton, Jan B. Hovener, Brian D. Ross</dc:creator><dc:identifier>10.1016/j.mri.2009.12.003</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-02-19</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-02-19</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09002781/abstract?rss=yes"><title>Model-based PRFS thermometry using fat as the internal reference and the extended Prony algorithm for model fitting - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09002781/abstract?rss=yes</link><description>Abstract: A model-based proton resonance frequency shift (PRFS) thermometry method was developed to significantly reduce the temperature quantification errors encountered in the conventional phase mapping method and the spatiotemporal limitations of the spectroscopic thermometry method. Spectral data acquired using multi-echo gradient echo (GRE) is fit into a two-component signal model containing temperature information and fat is used as the internal reference. The noniterative extended Prony algorithm is used for the signal fitting and frequency estimate. Monte Carlo simulations demonstrate the advantages of the method for optimal water-fat separation and temperature estimation accuracy. Phantom experiments demonstrate that the model-based method effectively reduces the interscan motion effects and frequency disturbances due to the main field drift. The thermometry result of ex vivo goose liver experiment with high intensity focused ultrasound (HIFU) heating was also presented in the paper to indicate the feasibility of the model-based method in real tissue.</description><dc:title>Model-based PRFS thermometry using fat as the internal reference and the extended Prony algorithm for model fitting - Corrected Proof</dc:title><dc:creator>Xinyi Pan, Cheng Li, Kui Ying, Dehe Weng, Wen Qin, Kuncheng Li</dc:creator><dc:identifier>10.1016/j.mri.2009.11.002</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-02-05</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-02-05</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09003129/abstract?rss=yes"><title>Improved B0 field map estimation for high field EPI - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09003129/abstract?rss=yes</link><description>Abstract: Echo planar imaging (EPI) is an ultrafast magnetic resonance imaging (MRI) technique that allows one to acquire a 2D image in about 100 ms. Unfortunately, the standard EPI images suffer from substantial geometric distortions, mainly originating from susceptibility differences in adjacent tissues. To reduce EPI distortions, correction methods based on a field map, which is a map of the off-resonance frequencies, have been developed. In this work, a nonlinear least squares estimator is used to optimize the estimation of the field map of the B0 field. The model of the EPI and reference data includes parameters for the phase evolution, the complex magnitude, the relaxation of the MRI signal and the EPI-specific phase difference between odd and even echoes, and from these parameters, additional corrections might be computed. The reference data required to estimate the field map can be acquired with a modified EPI-sequence. The proposed method is tested on simulated as well as experimental data and proves to be significantly more robust against noise, compared to the previously suggested method.</description><dc:title>Improved B0 field map estimation for high field EPI - Corrected Proof</dc:title><dc:creator>Dirk H.J. Poot, Wouter Pintjens, Marleen Verhoye, Annemie Van Der Linden, Jan Sijbers</dc:creator><dc:identifier>10.1016/j.mri.2009.12.020</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-02-05</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-02-05</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09003191/abstract?rss=yes"><title>Off-resonance frequency filtered magnetic resonance imaging - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09003191/abstract?rss=yes</link><description>Abstract: One of the main problems with rapid magnetic resonance imaging (MRI) techniques is the artifacts that result from off-resonance effects. The proposed off-resonance frequency filtered MRI (OFF-MRI) method focuses on the elimination of off-resonance components from the image of the observed object. To maintain imaging speed and simultaneously achieve good frequency selectivity, MRI is divided into two steps: signal acquisition and post-processing.After the preliminary phase in which we determine imaging parameters, MRI takes place; the signal from the same object is successively acquired M times. As a result, we obtain M partial signals in k-space, from which we form the image of the observed object in the post-processing phase, after signal acquisition has been completed. This paper demonstrates that with proper selection of acquisition parameters and weighting coefficients in the post-processing phase, OFF-MRI is equivalent to filtering the signal by finite impulse response filter of length M. It is shown that with M successive acquisitions M−1 off-resonance components can be eliminated (filtered-out) from images, and therefore, only two acquisitions are needed to eliminate one off-resonance components. On the other hand, with OFF-MRI, it is also possible to form the image of an arbitrary off-resonance component by eliminating all other off-resonance components, including the on-resonance component.The proposed OFF-MRI method is suitable for MRI where rapid acquisition is required and elimination of off-resonance components can improve reliability of measurements.</description><dc:title>Off-resonance frequency filtered magnetic resonance imaging - Corrected Proof</dc:title><dc:creator>Jure Medič, Sašo Tomažič</dc:creator><dc:identifier>10.1016/j.mri.2009.12.027</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-02-04</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-02-04</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09002859/abstract?rss=yes"><title>In vivo imaging of the human brain at 1.5 T with 0.6-mm isotropic resolution - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09002859/abstract?rss=yes</link><description>Abstract: We present high-resolution in vivo anatomical scans with 3D whole-brain coverage and an isotropic resolution of 0.6 mm, obtained at a clinical field of 1.5 T. The data are acquired in 10 independent scans over two sessions using a 3D magnetization-prepared, gradient echo sequence, modified to output phase images in addition to magnitude images. The independent scans are coregistered to correct for head motion, prior to performing complex averaging. The resolution of the final, averaged image, is found to be equal to the nominal one.The separation between the distribution of gray-scale values characterizing the gray and white matter, respectively, is substantially improved over single-scan images.Complex and magnitude averaging are compared and found to deliver similar results for regions with a high initial signal-to-noise ratio (SNR) within the brain. However, complex averaging is strongly recommended for quantitative applications or for studies where regions of low initial SNR are important.To summarize, a method for high-resolution in vivo anatomical imaging at a clinical field strength is demonstrated and is recommended for brain mapping. The method can also be applied at higher fields with a reduced acquisition time.</description><dc:title>In vivo imaging of the human brain at 1.5 T with 0.6-mm isotropic resolution - Corrected Proof</dc:title><dc:creator>Ana-Maria Oros-Peusquens, Tony Stoecker, Katrin Amunts, Karl Zilles, Nadim Jon Shah</dc:creator><dc:identifier>10.1016/j.mri.2009.11.006</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-02-01</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-02-01</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09002914/abstract?rss=yes"><title>An fMRI study of magnitude comparison and exact addition in children - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09002914/abstract?rss=yes</link><description>Abstract: By contrast to the adult literature, in which a consistent parietofrontal network for number processing has been identified, the data from studies of number processing in children have been less consistent, probably due to differences in study design and control conditions. Number processing was examined using functional magnetic resonance imaging in 18 right-handed children (8–12 years) from the Cape Coloured community in Cape Town, South Africa, using Proximity Judgment and Exact Addition (EA) tasks. The findings were consistent with the hypothesis that, as in adults, the anterior horizontal intraparietal sulcus (HIPS) plays a major role in the representation and manipulation of quantity in children. The posterior medial frontal cortex, believed to be involved in performance monitoring in more complex arithmetic manipulations in adults, was extensively activated even for relatively simple symbolic number processing in the children. Other areas activated to a greater degree in the children included the left precentral sulcus, which may mediate number knowledge and, for EA, the head of the caudate nucleus, which is part of a fronto-subcortical circuit involved in the behavioral execution of sequences. Two regions that have been linked to number processing in adults — the angular gyrus and posterior superior parietal lobule — were not activated in the children. The data are consistent with the inference that although the functional specialization of the anterior HIPS may increase as symbolic number processing becomes increasingly automatic, this region and other elements of the parietofrontal network identified in adults are already reliably and robustly activated by middle childhood.</description><dc:title>An fMRI study of magnitude comparison and exact addition in children - Corrected Proof</dc:title><dc:creator>Ernesta M. Meintjes, Sandra W. Jacobson, Christopher D. Molteno, J. Christopher Gatenby, Christopher Warton, Christopher J. Cannistraci, John C. Gore, Joseph L. Jacobson</dc:creator><dc:identifier>10.1016/j.mri.2009.11.010</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-02-01</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-02-01</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09002999/abstract?rss=yes"><title>Neural and vascular variability and the fMRI-BOLD response in normal aging - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09002999/abstract?rss=yes</link><description>Abstract: Neural, vascular and structural variables contributing to the blood oxygen level-dependent (BOLD) signal response variability were investigated in younger and older humans. Twelve younger healthy human subjects (six male and six female; mean age: 24 years; range: 19–27 years) and 12 older healthy subjects (five male and seven female; mean age: 58 years; range: 55–71 years) with no history of head trauma and neurological disease were scanned. Functional magnetic resonance imaging measurements using the BOLD contrast were made when participants performed a motor, cognitive or a breath hold (BH) task. Activation volume and the BOLD response amplitude were estimated for the younger and older at both group and subject levels. Mean activation volume was reduced by 45%, 40% and 38% in the elderly group during the motor, cognitive and BH tasks, respectively, compared to the younger. Reduction in activation volume was substantially higher compared to the reduction in the gray matter volume of 14% in the older compared to the younger. A significantly larger variability in the intersubject BOLD signal change occurred during the motor task, compared to the cognitive task. BH-induced BOLD signal change between subjects was significantly less-variable in the motor task-activated areas in the younger compared to older whereas such a difference between age groups was not observed during the cognitive task. Hemodynamic scaling using the BH signal substantially reduced the BOLD signal variability during the motor task compared to the cognitive task. The results indicate that the origin of the BOLD signal variability between subjects was predominantly vascular during the motor task while being principally a consequence of neural variability during the cognitive task. Thus, in addition to gray matter differences, the type of task performed can have different vascular variability weighting that can influence age-related differences in brain functional response.</description><dc:title>Neural and vascular variability and the fMRI-BOLD response in normal aging - Corrected Proof</dc:title><dc:creator>Sridhar S. Kannurpatti, Michael A. Motes, Bart Rypma, Bharat B. Biswal</dc:creator><dc:identifier>10.1016/j.mri.2009.12.007</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-02-01</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-02-01</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09003099/abstract?rss=yes"><title>Quantitative MR imaging of targeted SPIO particles on the cell surface and comparison to flow cytometry - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09003099/abstract?rss=yes</link><description>Abstract: Purpose: To detect anti-CEACAM5 targeted superparamagnetic iron oxide (SPIO) particles in vitro on the cell surface by quantitative magnetic resonance (MR) imaging and to compare with flow cytometry.Materials and Methods: The monoclonal mouse antibody T84.1 and an appropriate IgG isotype antibody were conjugated to dextran-coated SPIO particles. HT29 cells expressing carcinoembryonic antigen (CEACAM5) were treated with antibody-conjugated SPIO particles. Purified cell samples were examined on a 3.0-T MR scanner using a multi-echo spin-echo sequence for MR relaxometry. Aliquots of the cell samples were further treated with a fluorescein isothiocyanate (FITC) anti-dextran antibody and an Alexa Fluor 488 anti-mouse antibody for the corresponding flow cytometry.Results: MR relaxometry revealed a dose-dependent binding of T84.1-conjugated SPIO particles with a positive correlation between R2 relaxation rate of cell samples and SPIO particle concentration during incubation (r=0.993, P&lt;.01). Positive correlations were also observed between R2 relaxation rate and flow cytometry (geometric mean) with both fluorescent antibodies (r=0.972 and r=0.953, both P&lt;.01), respectively.Conclusion: The study revealed the feasibility of quantitative MR imaging of targeted SPIO particles on the cell surface comparable to flow cytometry.</description><dc:title>Quantitative MR imaging of targeted SPIO particles on the cell surface and comparison to flow cytometry - Corrected Proof</dc:title><dc:creator>Kersten Peldschus, Alexander Schultze, Peter Nollau, Michael Kaul, Udo Schumacher, Christoph Wagener, Gerhard Adam, Harald Ittrich</dc:creator><dc:identifier>10.1016/j.mri.2009.12.017</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-02-01</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-02-01</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09003154/abstract?rss=yes"><title>Changes in cerebral activity after decreased upper-limb hypertonus: an EMG-fMRI study - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09003154/abstract?rss=yes</link><description>Abstract: Objective: Whereas several studies have used functional magnetic resonance imaging (fMRI) to investigate motor recovery, whether therapy to decrease post-stroke hypertonus alters central motor patterns remains unclear. In this study, we used continuous electromyography (EMG)-fMRI to investigate possible changes in movement-related brain activation in patients receiving Botulinum toxin (BoNT-A) for hand-muscle hypertonus after chronic stroke.Methods: We studied eight stroke patients all of whom had hemiparesis and associated upper-limb hypertonus. All patients underwent an fMRI-EMG recording and clinical-neurological assessment before BoNT-A and 5 weeks thereafter. The handgrip motor task during imaging was fixed across both patients and controls. The movements were metronome paced, movement amplitude and force were controlled with a plastic orthosis, dynamometer and EMG recording. An age-matched control group was recruited from among healthy volunteers underwent the same fMRI-EMG recording.Results: Before BoNT-A, while patients moved the paretic hand, fMRI detected wide bilateral activation in the sensorymotor areas (SM1), in the supplementary motor area (SMA) and cerebellum. After BoNT-A blood oxygenation level-dependent (BOLD) activation decreased in ipsilateral and contralateral motor areas and became more lateralized. BOLD activation decreased also in ipsilateral cerebellar regions and in the SMA.Conclusion: Changes in peripheral upper-limb hypertonus after BoNT-A were associated to an improvement in active movements and more lateralized and focalized activation of motor areas. The clinical and EMG-fMRI coregistration technique we used to study hand-muscle hypertonus in patients receiving BoNT-A after chronic stroke should be useful in future studies seeking improved strategies for post-stroke neurorehabilitation.</description><dc:title>Changes in cerebral activity after decreased upper-limb hypertonus: an EMG-fMRI study - Corrected Proof</dc:title><dc:creator>Paolo Manganotti, Michele Acler, Emanuela Formaggio, Mirko Avesani, Franco Milanese, Andrea Baraldo, Silvia Francesca Storti, Anna Gasparini, Roberto Cerini, Roberto Pozzi Mucelli, Antonio Fiaschi</dc:creator><dc:identifier>10.1016/j.mri.2009.12.023</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-02-01</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-02-01</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09003166/abstract?rss=yes"><title>Frontoparietal activity with minimal decision and control in the awake macaque at 7 T - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09003166/abstract?rss=yes</link><description>Abstract: Previous imaging work has identified a frontoparietal network in the human brain involved in many different cognitive functions, as well as in simple updates of attended information. To determine whether a similar network is present in the monkey brain and direct future electrophysiological recordings, we examined the activation of frontoparietal areas during visual stimulation in the awake, fixating monkey. We measured activity with BOLD fMRI in three animals and analyzed the data individually for each animal and at group level. We found reliable activations in lateral prefrontal and parietal areas, even though task-related decision making was minimal, as a response to simple update of visual information. These activations were significant for each individual animal, as well as at group level. Similar to human imaging results the update of visual input was enough to activate an extensive network of frontoparietal cortex in the macaque brain, a network which is normally associated with complex cognitive control processes.</description><dc:title>Frontoparietal activity with minimal decision and control in the awake macaque at 7 T - Corrected Proof</dc:title><dc:creator>Steffen Stoewer, Shih-Pi Ku, Jozien Goense, Thomas Steudel, Nikos K. Logothetis, John Duncan, Natasha Sigala</dc:creator><dc:identifier>10.1016/j.mri.2009.12.024</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-02-01</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-02-01</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09003178/abstract?rss=yes"><title>A new automatic phase mask filter for high-resolution brain venography at 3 T: theoretical background and experimental validation - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09003178/abstract?rss=yes</link><description>Abstract: To improve vessel contrast in high-resolution susceptibility-based brain venography, an automatic phase contrast enhancing procedure is proposed, based on a new phase mask filter suitable for maximizing contrast of venous MR signals. The effectiveness of the new approach was assessed both on digital phantoms and on acquired MR human brain images, and then compared with venographic results of phase masking methods in recent literature. The digital phantom consisted of a simulated MR dataset with given signal-to-noise ratios (SNRs), while real human data were collected by scanning healthy volunteers with a 3.0-T MR system and a 3D gradient echo pulse sequence. The new phase mask (NM) was more effective than the conventional mask (CM) both on the digital phantoms and on the acquired MR images. A quantitative comparison based on phantom venograms indicates how this phase enhancement can lead to a significant increase in the contrast-to-noise ratio (CNR) for all considered phase values as well as for all vessel sizes of clinical interest. Likewise, the in vivo brain venograms reveal a better depiction of the smallest venous vessels and the enhancement of many details undetectable in conventional venograms.</description><dc:title>A new automatic phase mask filter for high-resolution brain venography at 3 T: theoretical background and experimental validation - Corrected Proof</dc:title><dc:creator>Sergio Casciaro, Roberto Bianco, Roberto Franchini, Ernesto Casciaro, Francesco Conversano</dc:creator><dc:identifier>10.1016/j.mri.2009.12.025</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-02-01</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-02-01</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09003002/abstract?rss=yes"><title>Detection of bone metastases using diffusion weighted magnetic resonance imaging: comparison with 11C-methionine PET and bone scintigraphy - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09003002/abstract?rss=yes</link><description>Abstract: Purpose: We evaluated the ability of diffusion-weighted imaging (DWI) to detect bone metastasis by comparing the results obtained using this modality with those obtained using 11C-methionine (MET) positron emission tomography (PET) and bone scintigraphy.Materials and methods: This retrospective study involved 29 patients with bone metastasis. DWI was obtained using a single-shot echo planar imaging (EPI) sequence with fat suppression using a short inversion time inversion recovery sequence. The detection capabilities of DWI for bone metastases were compared with those of whole body MET PET (in 19 patients) and 99mTc-methylene diphosphonate bone scintigraphy (in 15 patients).Results: Among the 19 patients who were diagnosed using DWI and PET, the PET identified 39 bone metastases, while the DWI identified 60 metastases out of 69 metastases revealed with conventional magnetic resonance imaging (MRI). Among the 15 patients who were diagnosed using DWI and bone scintigraphy, the bone scintigraphy identified 18 bone metastases, while the DWI identified 72 metastases out of 78 metastases revealed with conventional MRI. The overall bone metastasis detection rates were 56.5% for PET, 23.1% for bone scintigraphy and 92.3% for DWI.Conclusion: DWI is a very sensitive method for detecting bone metastasis and is superior to MET PET and bone scintigraphy in terms of its detection capabilities.</description><dc:title>Detection of bone metastases using diffusion weighted magnetic resonance imaging: comparison with 11C-methionine PET and bone scintigraphy - Corrected Proof</dc:title><dc:creator>Behnaz Goudarzi, Riwa Kishimoto, Shuhei Komatsu, Hiroyuki Ishikawa, Kyosan Yoshikawa, Susumu Kandatsu, Takayuki Obata</dc:creator><dc:identifier>10.1016/j.mri.2009.12.008</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-28</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-28</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X0900304X/abstract?rss=yes"><title>Brain MRI tissue classification based on local Markov random fields - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X0900304X/abstract?rss=yes</link><description>Abstract: A new method for tissue classification of brain magnetic resonance images (MRI) of the brain is proposed. The method is based on local image models where each models the image content in a subset of the image domain. With this local modeling approach, the assumption that tissue types have the same characteristics over the brain needs not to be evoked. This is important because tissue type characteristics, such as T1 and T2 relaxation times and proton density, vary across the individual brain and the proposed method offers improved protection against intensity non-uniformity artifacts that can hamper automatic tissue classification methods in brain MRI. A framework in which local models for tissue intensities and Markov Random Field (MRF) priors are combined into a global probabilistic image model is introduced. This global model will be an inhomogeneous MRF and it can be solved by standard algorithms such as iterative conditional modes. The division of the whole image domain into local brain regions possibly having different intensity statistics is realized via sub-volume probabilistic atlases. Finally, the parameters for the local intensity models are obtained without supervision by maximizing the weighted likelihood of a certain finite mixture model. For the maximization task, a novel genetic algorithm almost free of initialization dependency is applied. The algorithm is tested on both simulated and real brain MR images. The experiments confirm that the new method offers a useful improvement of the tissue classification accuracy when the basic tissue characteristics vary across the brain and the noise level of the images is reasonable. The method also offers better protection against intensity non-uniformity artifact than the corresponding method based on a global (whole image) modeling scheme.</description><dc:title>Brain MRI tissue classification based on local Markov random fields - Corrected Proof</dc:title><dc:creator>Jussi Tohka, Ivo D. Dinov, David W. Shattuck, Arthur W. Toga</dc:creator><dc:identifier>10.1016/j.mri.2009.12.012</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-28</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-28</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X0900318X/abstract?rss=yes"><title>Multimodal imaging: an evaluation of univariate and multivariate methods for simultaneous EEG/fMRI - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X0900318X/abstract?rss=yes</link><description>Abstract: The combination of electroencephalography (EEG) and functional magnetic resonance imaging (fMRI) has been proposed as a tool to study brain dynamics with both high temporal and high spatial resolution. Multimodal imaging techniques rely on the assumption of a common neuronal source for the different recorded signals. In order to maximally exploit the combination of these techniques, one needs to understand the coupling (i.e., the relation) between electroencephalographic (EEG) and fMRI blood oxygen level-dependent (BOLD) signals.Recently, simultaneous EEG-fMRI measurements have been used to investigate the relation between the two signals. Previous attempts at the analysis of simultaneous EEG-fMRI data reported significant correlations between regional BOLD activations and modulation of both event-related potential (ERP) and oscillatory EEG power, mostly in the alpha but also in other frequency bands.Beyond the correlation of the two measured brain signals, the relevant issue we address here is the ability of predicting the signal in one modality using information from the other modality. Using multivariate machine learning-based regression, we show how it is possible to predict EEG power oscillations from simultaneously acquired fMRI data during an eyes-open/eyes-closed task using either the original channels or the underlying cortically distributed sources as the relevant EEG signal for the analysis of multimodal data.</description><dc:title>Multimodal imaging: an evaluation of univariate and multivariate methods for simultaneous EEG/fMRI - Corrected Proof</dc:title><dc:creator>Federico De Martino, Giancarlo Valente, Aline W. de Borst, Fabrizio Esposito, Alard Roebroeck, Rainer Goebel, Elia Formisano</dc:creator><dc:identifier>10.1016/j.mri.2009.12.026</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-25</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-25</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09002860/abstract?rss=yes"><title>SNR-optimized myocardial perfusion imaging using parallel acquisition for effective density-weighted saturation recovery imaging - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09002860/abstract?rss=yes</link><description>Abstract: The concept of density-weighted imaging and parallel acquisition for effective density-weighted (PLANED) imaging was transferred to saturation recovery (SR) sequences, in order to increase the SNR in first-pass myocardial perfusion imaging. Filtering in combination with density-weighted imaging allows SNR-optimized data weighting and the free choice of the corresponding spatial response function (SRF) simultaneously. This method was evaluated in simulations and applied successfully to phantom and in vivo first-pass myocardial perfusion studies. Unfiltered, Cartesian sampled images were compared to images acquired with SR-PLANED, which has been adjusted to result in an identical SRF as the Cartesian imaging. SNR-optimized SR-PLANED imaging improved the SNR up to 15% without changing acquisition time, the SRF or the field of view (FOV). The presented method provides high image quality and optimized SNR for first-pass myocardial perfusion imaging.</description><dc:title>SNR-optimized myocardial perfusion imaging using parallel acquisition for effective density-weighted saturation recovery imaging - Corrected Proof</dc:title><dc:creator>Marcel Gutberlet, Oliver Geier, Daniel Stäb, Christian Ritter, Meinrad Beer, Dietbert Hahn, Herbert Köstler</dc:creator><dc:identifier>10.1016/j.mri.2009.11.007</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-22</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-22</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09002872/abstract?rss=yes"><title>Quantitative analysis of spatial distortions of diffusion techniques at 3T - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09002872/abstract?rss=yes</link><description>Abstract: Diffusion has been widely adopted in the clinical setting to study the microstructural tissue changes in conjunction with anatomic imaging and metabolic imaging to offer insights on the status of the tissue injury or lesion. However, geometric distortions caused by magnetic susceptibility effects, eddy currents and gradient imperfections greatly affect the clinical utility of the diffusion images. Several diffusion methods have been proposed in the recent years to obtain diffusion parameters with increased accuracy. In most cases, the comparisons to the clinical standard echo-planar imaging (EPI) diffusion are done visually without quantitative measurements. In this study, we present three simple, complementary quantitative methods of nonrigid image registration and shape analyses for evaluating spatial distortions on magnetic resonance images with application in comparing single-shot fast spin-echo (SSFSE) and EPI based diffusion measurements. These methods have confirmed the SSFSE based diffusion method is less distorted than the EPI based one, which is generally accepted through visual inspection.</description><dc:title>Quantitative analysis of spatial distortions of diffusion techniques at 3T - Corrected Proof</dc:title><dc:creator>Duan Xu, Michael C. Lee, Julio Carballido-Gamio, Matthew Barkovich, Sharmila Majumdar, Daniel B. Vigneron, Sarah J. Nelson</dc:creator><dc:identifier>10.1016/j.mri.2009.11.008</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-22</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-22</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09002975/abstract?rss=yes"><title>MR tracking of magnetically labeled mesenchymal stem cells in rats with liver fibrosis - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09002975/abstract?rss=yes</link><description>Abstract: Purpose: In vivo magnetic resonance (MR) tracking of magnetically labeled bone marrow mesenchymal stem cells (BMSCs) administered via the mesenteric vein to rats with liver fibrosis.Materials and Methods: Rat BMSCs were labeled with superparamagnetic iron oxide (SPIO) and the characteristics of the BMSCs after labeling were investigated. Eighteen rats with CCL4-induced liver fibrosis were randomized to three groups to receive SPIO-labeled BMSCs (BMSC-labeled group), cell-free SPIO (SPIO group), or unlabeled BMSCs (control group). MR imaging of the liver was performed at different time points, and signal-to-noise ratio (SNR) of the liver was measured. In vivo distribution of delivered BMSCs was assessed by histological analysis.Results: Labeling of BMSCs with SPIO did not significantly alter cell viability and proliferation activity. In BMSC-labeled group, the liver SNR immediately decreased from 8.56±0.26 to 3.53±0.41 at 1 h post injection and remained at a significantly lower level till 12 days (P&lt;.05 versus the level before). By contrast, the liver SNR of the SPIO group almost recovered to the preinjection level (P=.125) at 3 days after a transient decrease. In control group, the liver SNR demonstrated no significant difference at the tested time points. Additionally, Prussian blue-positive cells were mainly distributed in the liver parenchyma, especially in injured areas.Conclusion: The magnetically labeled BMSCs infused through the mesenteric vein can be detected in the fibrotic liver of rats using in vivo MR imaging up to 12 days after injection.</description><dc:title>MR tracking of magnetically labeled mesenchymal stem cells in rats with liver fibrosis - Corrected Proof</dc:title><dc:creator>Bin Zhou, Hong Shan, Dan Li, Zai-Bo Jiang, Jie-Sheng Qian, Kang-Shun Zhu, Ming-Sheng Huang, Xiao-Chun Meng</dc:creator><dc:identifier>10.1016/j.mri.2009.12.005</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-22</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-22</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09003063/abstract?rss=yes"><title>Respiratory noise correction using phase information - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09003063/abstract?rss=yes</link><description>Abstract: Respiratory noise is a confounding factor in functional magnetic resonance imaging (MRI) data analysis. A novel method called Respiratory noise Correction using Phase information is proposed to retrospectively correct for the respiratory noise in functional MRI (fMRI) time series. It is demonstrated that the respiratory movement and the phase of functional MRI images are highly correlated in time. The signal fluctuation due to respiratory movements can be effectively estimated from the phase variation and removed from the functional MRI time series using a Wiener filtering technique. In our experiments, this new method is compared with RETROICOR, which requires recording respiration signal simultaneously in an fMRI experiment. The two techniques show comparable performance with respect to the respiratory noise correction for fMRI time series. However, this technique is more advantageous because there is no need for monitoring the subjects’ respiration or changing functional MRI protocols. This technique is also potentially useful for correcting respiratory noise from abnormal breathing or when the respiration is not periodic.</description><dc:title>Respiratory noise correction using phase information - Corrected Proof</dc:title><dc:creator>Hu Cheng, Yu Li</dc:creator><dc:identifier>10.1016/j.mri.2009.12.014</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-22</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-22</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09003075/abstract?rss=yes"><title>Validation of the anisotropy index ellipsoidal area ratio in diffusion tensor imaging - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09003075/abstract?rss=yes</link><description>Abstract: A new diffusion anisotropy index, ellipsoidal area ratio (EAR), was described recently and proved to be less noise-sensitive than fractional anisotropy (FA) by theory and simulation. Here we show that EAR has higher signal-to-noise ratios than FA in average diffusion tensor imaging data from 40 normal subjects. EAR was also more sensitive than FA in detecting white matter abnormalities in a patient with widespread diffuse axonal injury. Monte Carlo simulation showed that EAR's mean values are more biased by noise than FA when anisotropy is small, both for single fiber tracts and when fiber tracts cross. However, the improved signal-to-noise ratio of EAR relative to FA suggests that EAR may be a superior measure of anisotropy both in quantifying both deep white matter with relatively uniform fiber tracts and pericortical white matter structure with relatively low anisotropy and fiber crossings.</description><dc:title>Validation of the anisotropy index ellipsoidal area ratio in diffusion tensor imaging - Corrected Proof</dc:title><dc:creator>Xiaojian Kang, Timothy J. Herron, David L. Woods</dc:creator><dc:identifier>10.1016/j.mri.2009.12.015</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-22</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-22</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09003087/abstract?rss=yes"><title>Relationship between neural and hemodynamic signals during spontaneous activity studied with temporal kernel CCA - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09003087/abstract?rss=yes</link><description>Abstract: Functional magnetic resonance imaging (fMRI) based on the so-called blood oxygen level-dependent (BOLD) contrast is a powerful tool for studying brain function not only locally but also on the large scale. Most studies assume a simple relationship between neural and BOLD activity, in spite of the fact that it is important to elucidate how the “when” and “what” components of neural activity are correlated to the “where” of fMRI data. Here we conducted simultaneous recordings of neural and BOLD signal fluctuations in primary visual (V1) cortex of anesthetized monkeys. We explored the neurovascular relationship during periods of spontaneous activity by using temporal kernel canonical correlation analysis (tkCCA). tkCCA is a multivariate method that can take into account any features in the signals that univariate analysis cannot. The method detects filters in voxel space (for fMRI data) and in frequency–time space (for neural data) that maximize the neurovascular correlation without any assumption of a hemodynamic response function (HRF). Our results showed a positive neurovascular coupling with a lag of 4–5 s and a larger contribution from local field potentials (LFPs) in the γ range than from low-frequency LFPs or spiking activity. The method also detected a higher correlation around the recording site in the concurrent spatial map, even though the pattern covered most of the occipital part of V1. These results are consistent with those of previous studies and represent the first multivariate analysis of intracranial electrophysiology and high-resolution fMRI.</description><dc:title>Relationship between neural and hemodynamic signals during spontaneous activity studied with temporal kernel CCA - Corrected Proof</dc:title><dc:creator>Yusuke Murayama, Felix Bieβmann, Frank C. Meinecke, Klaus-Robert Müller, Mark Augath, Axel Oeltermann, Nikos K. Logothetis</dc:creator><dc:identifier>10.1016/j.mri.2009.12.016</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-22</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-22</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09003117/abstract?rss=yes"><title>Development of a high-precision image-processing automatic measurement system for MRI visceral fat images acquired using a binomial RF-excitation pulse - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09003117/abstract?rss=yes</link><description>Abstract: Development of a rapid and accurate method for visceral fat measurement is an important task, given the recent increase in the number of patients with metabolic syndrome. In this study, we optimized the Fast Low Angle Shot (FLASH) sequence using a binominal radiofrequency excitation pulse, in which the acquisition time is short, and measured changes in the amount of visceral fat in subjects after a period of wearing clothes with a fat-reducing effect during walking. We solved the reproducibility problem associated with the number of slices, and developed automatic measurement software for high-precision separation and extraction of abdominal visceral fat images. This software was developed using intensity correction with the coil position, derivation of a threshold by histogram analysis and fat separation by template matching for abdominal images. The cross-sectional area of a single slice varies for every acquisition due to visceral organ movement, but the relative error largely converged for seven slices. The measured amount of abdominal fat tended to be consistent with changes in the body fat and waist circumference of the subjects. The correlation coefficients between automatic extraction using the measurement software and manual extraction were 0.9978 for subcutaneous fat and 0.9972 for visceral fat, showing very strong positive correlations. The consistency rates were 0.9502±0.0167 for subcutaneous fat and 0.9395±0.0147 for visceral fat, and the shapes of the regions were also extracted very accurately. These results show that the magnetic resonance imaging acquisition method and image processing system developed in this study are beneficial for measurement of abdominal visceral fat. Therefore, this method may have a major role in future diagnosis of metabolic syndrome.</description><dc:title>Development of a high-precision image-processing automatic measurement system for MRI visceral fat images acquired using a binomial RF-excitation pulse - Corrected Proof</dc:title><dc:creator>Ryusuke Nakai, Takashi Azuma, Taizou Kishimoto, Tazuko Hirata, Osamu Takizawa, Suong-Hyu Hyon, Sadami Tsutsumi</dc:creator><dc:identifier>10.1016/j.mri.2009.12.019</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-22</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-22</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09003130/abstract?rss=yes"><title>Classifier ensembles for fMRI data analysis: an experiment - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09003130/abstract?rss=yes</link><description>Abstract: Functional magnetic resonance imaging (fMRI) is becoming a forefront brain–computer interface tool. To decipher brain patterns, fast, accurate and reliable classifier methods are needed. The support vector machine (SVM) classifier has been traditionally used. Here we argue that state-of-the-art methods from pattern recognition and machine learning, such as classifier ensembles, offer more accurate classification. This study compares 18 classification methods on a publicly available real data set due to Haxby et al. [Science 293 (2001) 2425–2430]. The data comes from a single-subject experiment, organized in 10 runs where eight classes of stimuli were presented in each run. The comparisons were carried out on voxel subsets of different sizes, selected through seven popular voxel selection methods. We found that, while SVM was robust, accurate and scalable, some classifier ensemble methods demonstrated significantly better performance. The best classifiers were found to be the random subspace ensemble of SVM classifiers, rotation forest and ensembles with random linear and random spherical oracle.</description><dc:title>Classifier ensembles for fMRI data analysis: an experiment - Corrected Proof</dc:title><dc:creator>Ludmila I. Kuncheva, Juan J. Rodríguez</dc:creator><dc:identifier>10.1016/j.mri.2009.12.021</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-22</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-22</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09003142/abstract?rss=yes"><title>Behavioral, electrophysiological and histopathological consequences of systemic manganese administration in MEMRI - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09003142/abstract?rss=yes</link><description>Abstract: Manganese (Mn2+)-enhanced magnetic resonance imaging (MEMRI) offers the possibility to generate longitudinal maps of brain activity in unrestrained and behaving animals. However, Mn2+ is a metabolic toxin and a competitive inhibitor for Ca2+, and therefore, a yet unsolved question in MEMRI studies is whether the concentrations of metal ion used may alter brain physiology. In the present work we have investigated the behavioral, electrophysiological and histopathological consequences of MnCl2 administration at concentrations and dosage protocols regularly used in MEMRI. Three groups of animals were sc injected with saline, 0.1 and 0.5 mmol/kg MnCl2, respectively. In vivo electrophysiological recordings in the hippocampal formation revealed a mild but detectable decrease in both excitatory postsynaptic potentials (EPSP) and population spike (PS) amplitude under the highest MnCl2 dose. The EPSP to PS ratio was preserved at control levels, indicating that neuronal excitability was not affected. Experiments of pair pulse facilitation demonstrated a dose dependent increase in the potentiation of the second pulse, suggesting presynaptic Ca2+ competition as the mechanism for the decreased neuronal response. Tetanization of the perforant path induced a long-term potentiation of synaptic transmission that was comparable in all groups, regardless of treatment. Accordingly, the choice accuracy tested on a hippocampal-dependent learning task was not affected. However, the response latency in the same task was largely increased in the group receiving 0.5 mmol/kg of MnCl2. Immunohistological examination of the hippocampus at the end of the experiments revealed no sign of neuronal toxicity or glial reaction. Although we show that MEMRI at 0.1 mmol/Kg MnCl2 may be safely applied to the study of cognitive networks, a detailed assessment of toxicity is strongly recommended for each particular study and Mn2+ administration protocol.</description><dc:title>Behavioral, electrophysiological and histopathological consequences of systemic manganese administration in MEMRI - Corrected Proof</dc:title><dc:creator>Oxana Eschenko, Santiago Canals, Irina Simanova, Nikos K. Logothetis</dc:creator><dc:identifier>10.1016/j.mri.2009.12.022</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-22</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-22</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09002823/abstract?rss=yes"><title>Quantitative multivoxel proton chemical shift imaging of the breast - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09002823/abstract?rss=yes</link><description>Abstract: The study of focal pathology by single-voxel magnetic resonance spectroscopy (MRS) is hampered by the impossibility to study tissue heterogeneity or compare the metabolite signals in breast lesion directly to those in unaffected tissue. Multivoxel MRS studies, while potentially allowing for truly quantitative tissue characterization, have up to now also been far from quantitative with, for example, the signal-to-noise ratio of the choline (Cho) signal serving as measure of tumor activity. Shown in this study is that in a standard clinical setting with a regular 1.5-T magnetic resonance scanner, it is possible to perform quantitative multivoxel MRS. With the use of literature values for the T1 and T2 relaxation times of Cho and water in fibroglandular breast tissue and tumors, one can determine the concentrations of Cho in different tumor compartments and surrounding tissues in two brief multivoxel MRS measurements. This opens excellent perspectives to quantitative diagnostic and follow-up studies of focal pathology such as lesions suspected of breast cancer.</description><dc:title>Quantitative multivoxel proton chemical shift imaging of the breast - Corrected Proof</dc:title><dc:creator>Paul E. Sijens, Monique D. Dorrius, Peter Kappert, Paul Baron, Ruud M. Pijnappel, Matthijs Oudkerk</dc:creator><dc:identifier>10.1016/j.mri.2009.11.004</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-14</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-14</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09002902/abstract?rss=yes"><title>Exploring vision-related acupuncture point specificity with multivoxel pattern analysis - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09002902/abstract?rss=yes</link><description>Abstract: Acupoint specificity is one of the central issues of functional magnetic resonance imaging (fMRI) studies of acupuncture and has been under discussed. However, strong and consistent proof has not been provided for the existence of acupoint specificity, and unsuitable analysis approach applied could be the reason. We observed that previous researches of acupoint specificity were mostly based on model-based methods which were limited to make exploration of acupoint specificity because of the inaccurate specified prior. Here we applied multi-voxel pattern analysis (MVPA) to investigate the specificity of brain activation patterns induced by acupuncture stimulations at a vision-related acupoint (GB37) and a nearby nonacupoint (NAP). Results showed that multiple brain areas could differentiate the central neural response patterns induced by acupuncture stimulation at these two sites with higher accuracy above the chance level. These regions included occipital cortex, limbic-cerebellar areas and somatosensory cortex. Our results support that the characteristic neural response patterns of brain cortex to the acupuncture stimulation at GB37 and a nearby NAP could differ from each other effectively with the application of MVPA approach.</description><dc:title>Exploring vision-related acupuncture point specificity with multivoxel pattern analysis - Corrected Proof</dc:title><dc:creator>Linling Li, Wei Qin, Lijun Bai, Jie Tian</dc:creator><dc:identifier>10.1016/j.mri.2009.11.009</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-14</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-14</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09002926/abstract?rss=yes"><title>EEG topography-specific BOLD changes: a continuous EEG-fMRI study in a patient with focal epilepsy - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09002926/abstract?rss=yes</link><description>Abstract: Blood oxygenation level dependent (BOLD) response related to interictal activity was evaluated in a patient with post-traumatic focal epilepsy at repeated continuous electroencephalogram (EEG)-functional magnetic resonance imaging examinations. Lateralized interictal EEG activity induced a main cluster of activation co-localized with the anatomical lesion. Spreading of EEG interictal activity to both frontal lobes evoked bilateral clusters of activation indicating that topography of BOLD response might depend on the spatial distribution of epileptiform activity.</description><dc:title>EEG topography-specific BOLD changes: a continuous EEG-fMRI study in a patient with focal epilepsy - Corrected Proof</dc:title><dc:creator>Mirco Cosottini, Ilaria Pesaresi, Patrizia Maritato, Gina Belmonte, Arianna Taddei, Ferdinando Sartucci, Mario Mascalchi, Luigi Murri</dc:creator><dc:identifier>10.1016/j.mri.2009.11.011</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-14</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-14</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X0900294X/abstract?rss=yes"><title>Experimental hypoxic–ischemic encephalopathy: comparison of apparent diffusion coefficients and proton magnetic resonance spectroscopy - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X0900294X/abstract?rss=yes</link><description>Abstract: This study aims to compare the apparent diffusion coefficients (ADCs) and proton magnetic resonance spectroscopy (1H-MRS) in the first 24 h of acute hypoxic-ischemic brain damage (HIBD) in piglets. Twenty-five 7-day-old piglets were subjected to transient bilateral common carotid artery occlusion followed by ventilation with 4% oxygen for 1 h. Diffusion-weighted imaging (DWI) and 1H-MRS were performed on cessation of the insult or at 3, 6, 12 or 24 h after resuscitation (all n=5). ADCs, N-acetylaspartate/choline (NAA/Cho), NAA/creatine (NAA/Cr), lactate/NAA (Lac/NAA), Lac/Cho and Lac/Cr were calculated. Cerebral injury was evaluated by pathological study and Hsp70 immunohistochemical analysis. On cessation of the insult, ADCs, NAA/Cho and NAA/Cr reduced, Lac/NAA, Lac/Cho and Lac/Cr increased. From 3 to 12 h after resuscitation, ADCs, Lac/NAA, Lac/Cho and Lac/Cr recovered, NAA/Cho and NAA/Cr reduced. Twenty-four hours after resuscitation, ADCs reduced once more, Lac/NAA, Lac/Cho and Lac/Cr increased again, whereas NAA/Cho and NAA/Cr decreased continuously. Pathological study revealed mild cerebral edema on cessation of the insult and more and more severe cerebral injury after resuscitation. No Hsp70-positive cells were detected on cessation of the insult. From 3 to 12 hours after resuscitation, Hsp70-positive cells gradually increased. Twenty-four hours after resuscitation, Hsp70-positive cells decreased. Throughout the experiment, changes in NAA/Cho and pathology had the best correlation (R=–0.729). In conclusion, NAA/Cho is the most precise ratio to reflect the pathological changes of early HIBD. Transient ADCs and Lac ratios recovery do not predict the reversal of histological damage of early HIBD. Reducing astrocytic swelling is of great clinical significance.</description><dc:title>Experimental hypoxic–ischemic encephalopathy: comparison of apparent diffusion coefficients and proton magnetic resonance spectroscopy - Corrected Proof</dc:title><dc:creator>Yang-Kang Li, Guo-Rui Liu, Xiu-Guo Zhou, Ai-Qun Cai</dc:creator><dc:identifier>10.1016/j.mri.2009.12.002</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-14</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-14</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09002963/abstract?rss=yes"><title>Double-spin-echo diffusion weighting with a modified eddy current adjustment - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09002963/abstract?rss=yes</link><description>Abstract: Magnetic field inhomogeneities like eddy current-related gradient fields cause geometric distortions in echo-planar imaging (EPI). This in particular affects diffusion-weighted imaging where these distortions vary with the direction of the diffusion weighting and hamper the accurate determination of diffusion parameters. The double-spin-echo preparation often used aims to reduce the cumulative eddy current effect by adjusting the diffusion-weighting gradient pulse durations to the time constant of the dominant eddy current contribution. However, eddy currents with a variety of time constants may be present and cause residual distortions. Here, a modification is proposed where the two bipolar gradient pairs of the preparation are adjusted independently to different time constants. At the expense of a slightly prolonged echo time, residual geometric distortions and correspondingly increased values of the diffusion anisotropy can be reduced as is demonstrated in phantoms and the human brain. Thus, it may help to improve the reliability of diffusion-weighted EPI.</description><dc:title>Double-spin-echo diffusion weighting with a modified eddy current adjustment - Corrected Proof</dc:title><dc:creator>Jürgen Finsterbusch</dc:creator><dc:identifier>10.1016/j.mri.2009.12.004</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-14</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-14</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09003038/abstract?rss=yes"><title>Unfolding the long-term pathophysiological processes following an acute inflammatory demyelinating lesion of multiple sclerosis - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09003038/abstract?rss=yes</link><description>Abstract: Background: Acute symptomatic inflammation is a main feature of multiple sclerosis but pathophysiological processes underlying total or partial recovery are poorly understood.Objective: To characterize in vivo these processes at molecular, structural and functional levels using multimodal MR methods.Methods: A neuroimaging 3-year follow-up (Weeks 0, 3, 11, 29, 59 and 169) was conducted on a 41-year-old woman presenting at baseline with a large acute demyelinating lesion of multiple sclerosis. Conventional magnetic resonance imaging (MRI), magnetization transfer imaging, diffusion-weighted imaging, functional MRI and magnetic resonance spectroscopy were conducted at 1.5 T.Results: Patient presenting with subacute left hemiplegia recovered progressively (expended disability status scale 7 to 5.5). The MR exploration demonstrated structural functional and metabolic impairments at baseline. Despite restoration of the blood brain barrier integrity, high lactate levels persisted for several weeks concomitant with glial activation. Slow and progressive structural and metabolic restorations occurred from baseline to W169 (lesion volume −64%; apparent diffusion coefficient −14.7%, magnetization transfer ratio +14%, choline −51%, lipids −78%, N-acetylaspartate +77%) while functionality of the motor system recovered.Conclusions: Multimodal MRI/MRS evidenced long-term dynamics recovery processes involving tissue repair, glial activation, recovery of neuronal function and functional systems. This may impact on customized rehabilitation strategies generally focused on the first months following the onset of symptoms.</description><dc:title>Unfolding the long-term pathophysiological processes following an acute inflammatory demyelinating lesion of multiple sclerosis - Corrected Proof</dc:title><dc:creator>Wafaa Zaaraoui, Audrey Rico, Bertrand Audoin, Françoise Reuter, Irina Malikova, Elisabeth Soulier, Patrick Viout, Yann Le Fur, Sylviane Confort-Gouny, Patrick J. Cozzone, Jean Pelletier, Jean-Philippe Ranjeva</dc:creator><dc:identifier>10.1016/j.mri.2009.12.011</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-14</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-14</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X0900277X/abstract?rss=yes"><title>Quantitative evaluation of optimal imaging parameters for single-cell detection in MRI using simulation - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X0900277X/abstract?rss=yes</link><description>Abstract: Super-paramagnetic iron oxide (SPIO) nanoparticles are actively investigated to enhance disease detection through molecular imaging using magnetic resonance imaging (MRI). Detection of the cells labeled by SPIO depends on the MRI protocols and pulse sequence parameters that can be optimized. To evaluate the sensitivity and specificity of the image acquisition methods and to obtain optimal imaging parameters for single-cell detection, we further developed an MRI simulator. The simulator models an object (tissue) at a microscopic level to evaluate effects of spatial distribution and concentration of nanoparticles on the resulting image. In this study, the simulator was used to evaluate and compare imaging of the labeled cells by the gradient-echo (GE), true-FISP [fast imaging employing steady-state acquisition (FIESTA)] and echo-planar imaging (EPI) pulse sequences. Effects of the imaging and object parameters, such as field strength, imaging protocol and pulse sequence parameters, imaging resolution, cell iron load, position of SPIO within the voxel and cell division within the voxel, were investigated in the work. The results suggest that true-FISP has the highest sensitivity for single-cell detection by MRI.</description><dc:title>Quantitative evaluation of optimal imaging parameters for single-cell detection in MRI using simulation - Corrected Proof</dc:title><dc:creator>Ali-Reza Mohammadi-Nejad, Gholam-Ali Hossein-Zadeh, Hamid Soltanian-Zadeh</dc:creator><dc:identifier>10.1016/j.mri.2009.11.001</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-11</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-11</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09002835/abstract?rss=yes"><title>Diffusion tensor magnetic resonance imaging of the normal breast - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09002835/abstract?rss=yes</link><description>Abstract: Purpose: The objective of this study was to evaluate diffusion anisotropy of the breast parenchyma and assess the range and repeatability of diffusion tensor imaging (DTI) parameters in normal breast tissue.Materials and Methods: The study was approved by our institutional review board and included 12 healthy females (median age, 36 years). Diffusion tensor imaging was performed at 1.5 T using a diffusion-weighted echo planar imaging sequence. Diffusion tensor imaging parameters including tensor eigenvalues (λ1, λ2, λ3), fractional anisotropy (FA) and apparent diffusion coefficient (ADC) were measured for anterior, central and posterior breast regions.Results: Mean normal breast DTI measures were λ1=2.51×10−3 mm2/s, λ2=1.89×10−3 mm2/s, λ3=1.39×10−3 mm2/s, ADC=1.95±0.24×10−3 mm2/s and FA=0.29±0.05 for b=600 s/mm2. Significant regional differences were observed for both FA and ADC (P&lt;.05), with higher ADC in the central breast and higher FA in the posterior breast. Comparison of DTI values calculated using b=0, 600 s/mm2 vs. b=0, 1000 s/mm2, showed significant differences in ADC (P&lt;.001), but not FA. Repeatability assessment produced within-subject coefficient of variations of 4.5% for ADC and 11.4% for FA measures.Conclusion: This study demonstrates anisotropy of water diffusion in normal breast tissue and establishes a normative range of breast FA values. Attention to the influence of breast region and b value on breast DTI measurements may be important for clinical interpretation and standardization of techniques.</description><dc:title>Diffusion tensor magnetic resonance imaging of the normal breast - Corrected Proof</dc:title><dc:creator>Savannah C. Partridge, Revathi S. Murthy, Ali Ziadloo, Steven W. White, Kimberly H. Allison, Constance D. Lehman</dc:creator><dc:identifier>10.1016/j.mri.2009.10.003</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-11</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-11</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09002847/abstract?rss=yes"><title>A method for automatic identification of water and fat images from a symmetrically sampled dual-echo Dixon technique - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09002847/abstract?rss=yes</link><description>Abstract: Sampling water and fat signals symmetrically (i.e., at 0° and 180° relative phase angles) in a dual-echo Dixon technique offers high intrinsic tolerance to phase fluctuations in postprocessing and maximum signal-to-noise performance for the separated water and fat images. However, identification of which image is water and which image is fat after their separation is not possible based on the phase information alone. In this work, we proposed a semiempirical automatic image identification method that is based on the intrinsic asymmetry between the water and fat chemical shift spectra. Specifically, the approximately bimodal feature of the fat spectra and the observation that most in vivo tissues are either predominantly water or predominantly fat are used to construct a spectrum-based algorithm. Additional refinement is accomplished by considering the spatial distribution of the tissues that may have a coexistence of water and fat. The final improved algorithm was tested on a total of 131 three-dimensional patient datasets collected from different scanners and found to yield correct water and fat identification in all datasets.</description><dc:title>A method for automatic identification of water and fat images from a symmetrically sampled dual-echo Dixon technique - Corrected Proof</dc:title><dc:creator>Moiz Ahmad, Yinan Liu, Zachary W. Slavens, Russell Low, Elmar Merkle, Ken-Pin Hwang, Anthony Vu, Jingfei Ma</dc:creator><dc:identifier>10.1016/j.mri.2009.11.005</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-11</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-11</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09002938/abstract?rss=yes"><title>Assessment of cardiac iron by MRI susceptometry and R2* in patients with thalassemia - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09002938/abstract?rss=yes</link><description>Abstract: A magnetic resonance imaging cardiac magnetic susceptometry (MRI-CS) technique for assessing cardiac tissue iron concentration based on phase mapping was developed. Normal control subjects (n=9) and thalassemia patients (n=13) receiving long-term blood transfusion therapy underwent MRI-CS and MRI measurements of the cardiac relaxation rate R2*. Using MRI-CS, subepicardium and subendocardium iron concentrations were quantified exploiting the hemosiderin/ferritin iron specific magnetic susceptibility. The average of subepicardium and subendocardium iron concentrations and R2* of the septum were found to be strongly correlated (r=0.96, P&lt;.0001), and linear regression analysis yielded CIC (μg Fe/gwet tissue)=(6.4±0.4)·R2* septum (s−1) − (120±40). The results demonstrated that septal R2* indeed measures cardiac iron level.</description><dc:title>Assessment of cardiac iron by MRI susceptometry and R2* in patients with thalassemia - Corrected Proof</dc:title><dc:creator>Zhiyue J. Wang, Roland Fischer, Zili Chu, Donald H. Mahoney, Brigitta U. Mueller, Raja Muthupillai, Ellen B. James, Rajesh Krishnamurthy, Taylor Chung, Eric Padua, Elliott Vichinsky, Paul Harmatz</dc:creator><dc:identifier>10.1016/j.mri.2009.12.001</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-11</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-11</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09002987/abstract?rss=yes"><title>On the measurement of multi-component T2 relaxation in cartilage by MR spectroscopy and imaging - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09002987/abstract?rss=yes</link><description>Abstract: The multicomponent T2 relaxation in bovine nasal cartilage (BNC) was investigated by nuclear magnetic resonance spectroscopy using the Carr-Purcell-Meiboom-Gill (CPMG) sequence and microscopic magnetic resonance imaging (μMRI) method using a CPMG-SE imaging sequence. All experimental data were analyzed by the non-negative least square (NNLS) procedure. Only one T2 component was found in BNC by both experimental methods (about 113 and 170 ms before and after being enzymatically digested by trypsin). Several experimental and specimen-related factors were investigated in this study, and it was found that some of them could produce artificial multi-component T2, including the use of the standard MSME imaging sequence at certain imaging gradients.</description><dc:title>On the measurement of multi-component T2 relaxation in cartilage by MR spectroscopy and imaging - Corrected Proof</dc:title><dc:creator>ShaoKuan Zheng, Yang Xia</dc:creator><dc:identifier>10.1016/j.mri.2009.12.006</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-11</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-11</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09003014/abstract?rss=yes"><title>Determining uterine blood flow in pregnancy with magnetic resonance imaging - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09003014/abstract?rss=yes</link><description>Abstract: Objective: The purpose of this study is to determine the feasibility of measuring total uterine blood flow in pregnancy using magnetic resonance imaging (MRI) technique.Methods: Uterine blood flow was determined in pregnant women in whom MRI was being carried out to assess a fetal anomaly. A two-dimensional time-of-flight magnetic resonance (MR) angiogram sequence was performed. Scout images and a peripherally gated phase contrast MR sequence were planned to study simultaneous blood flow in the uterine and ovarian arteries.Results: The MR pelvic angiogram sequence was completed in 13 women. The uterine arteries were visualized and their cross-sectional area determined. The complexity of the pelvic blood supply prevented the calculation of blood flow velocity and, thus, total uterine blood flow.Conclusion: The measurement of total uterine blood flow during pregnancy was not possible using our MR technique. The ovarian vessels were not consistently visualized. Doppler ultrasonography remains the best modality by which to estimate total uterine blood flow in pregnancy.</description><dc:title>Determining uterine blood flow in pregnancy with magnetic resonance imaging - Corrected Proof</dc:title><dc:creator>Jason A. Pates, Mustapha R. Hatab, Donald D. McIntire, F. Gary Cunningham, Diane M. Twickler</dc:creator><dc:identifier>10.1016/j.mri.2009.12.009</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-11</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-11</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09003051/abstract?rss=yes"><title>Incidental abdominal aortic aneurysm on lumbosacral magneticresonance imaging — a case series - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09003051/abstract?rss=yes</link><description>Abstract: Magnetic resonance imaging (MRI) is commonly used as part of the assessment of patients presenting with leg/back pain to the orthopedic spinal outpatient clinic. Abdominal aortic aneurysm (AAA) can cause symptoms often similar to those of spinal stenosis. We report a case series of four patients who had incidental AAA detected on lumbosacral MRI. All patients were suffering from degenerative spinal disease and had been referred to the orthopedic spinal clinic. After history, examination and review of the imaging, all patients were referred to a vascular surgeon, and three were found to be completely asymptomatic from their aneurysm. One patient required open repair with an aortic graft due to the size of the aneurysm, although his symptoms were attributable to his spinal disease. All patients still required management of their degenerative spinal disease after their vascular review. We can find no other case reports of AAA as an incidental finding on lumbosacral MRI. This case series highlights the importance of looking at all aspects of our imaging and remembering the nonspinal causes of back and leg pains. Furthermore, in the presence of AAA when managing patients in the orthopedic outpatient setting, the authors recommend vascular review before offering orthopedic interventional management options to these patients.</description><dc:title>Incidental abdominal aortic aneurysm on lumbosacral magneticresonance imaging — a case series - Corrected Proof</dc:title><dc:creator>Alex J. Trompeter, Guy P. Paremain</dc:creator><dc:identifier>10.1016/j.mri.2009.12.013</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-11</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-11</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09003105/abstract?rss=yes"><title>Cardiac magnetic resonance imaging using radial k-space sampling and self-calibrated partial parallel reconstruction - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09003105/abstract?rss=yes</link><description>Abstract: Radial sampling has been demonstrated to be potentially useful in cardiac magnetic resonance imaging because it is less susceptible to motion than Cartesian sampling. Nevertheless, its capability of imaging acceleration remains limited by undersampling-induced streaking artifacts. In this study, a self-calibrated reconstruction method was developed to suppress streaking artifacts for highly accelerated parallel radial acquisitions in cardiac magnetic resonance imaging. Two- (2D) and three-dimensional (3D) radial k-space data were collected from a phantom and healthy volunteers. Images reconstructed using the proposed method and the conventional regridding method were compared based on statistical analysis on a four-point scale imaging scoring. It was demonstrated that the proposed method can effectively remove undersampling streaking artifacts and significantly improve image quality (P&lt;.05). With the use of the proposed method, image score (1–4, 1=poor, 2=good, 3=very good, 4=excellent) was improved from 2.14 to 3.34 with the use of an undersampling factor of 4 and from 1.09 to 2.5 with the use of an undersampling factor of 8. Our study demonstrates that the proposed reconstruction method is effective for highly accelerated cardiac imaging applications using parallel radial acquisitions without calibration data.</description><dc:title>Cardiac magnetic resonance imaging using radial k-space sampling and self-calibrated partial parallel reconstruction - Corrected Proof</dc:title><dc:creator>Jingsi Xie, Peng Lai, Feng Huang, Yu Li, Debiao Li</dc:creator><dc:identifier>10.1016/j.mri.2009.12.018</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-11</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-11</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X0900280X/abstract?rss=yes"><title>Initial in vivo rodent sodium and proton MR imaging at 21.1 T - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X0900280X/abstract?rss=yes</link><description>Abstract: The first in vivo sodium and proton magnetic resonance (MR) images and localized spectra of rodents were attained using the wide bore (105 mm) high resolution 21.1-T magnet, built and operated at the National High Magnetic Field Laboratory (Tallahassee, FL, USA). Head images of normal mice (C57BL/6J) and Fisher rats (∼250 g) were acquired with custom designed radiofrequency probes at frequencies of 237/900 MHz for sodium and proton, respectively. Sodium MR imaging resolutions of ∼0.125 μl for mouse and rat heads were achieved by using a 3D back-projection pulse sequence. A gain in SNR of ∼3 for sodium and ∼2 times for proton were found relative to corresponding MR images acquired at 9.4 T. 3D Fast Low Angle Shot (FLASH) proton mouse images (50×50×50 μm3) were acquired in 90 min and corresponding rat images (100×100×100 μm3) within a total time of 120 min. Both in vivo large rodent MR imaging and localized spectroscopy at the extremely high field of 21.1 T are feasible and demonstrate improved resolution and sensitivity valuable for structural and functional brain analysis.</description><dc:title>Initial in vivo rodent sodium and proton MR imaging at 21.1 T - Corrected Proof</dc:title><dc:creator>Victor D. Schepkin, William W. Brey, Peter L. Gor'kov, Samuel C. Grant</dc:creator><dc:identifier>10.1016/j.mri.2009.10.002</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-04</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-04</prism:publicationDate></item><item rdf:about="http://www.mrijournal.com/article/PIIS0730725X09002811/abstract?rss=yes"><title>Quantitative SENSE-MRSI of the human brain - Corrected Proof</title><link>http://www.mrijournal.com/article/PIIS0730725X09002811/abstract?rss=yes</link><description>Abstract: Purpose: To develop a method for estimating metabolite concentrations using phased-array coils and sensitivity-encoded (SENSE) magnetic resonance spectroscopic images (MRSI) of the human brain.Materials and Methods: The method is based on the phantom replacement technique and uses receive coil sensitivity maps and body-coil loading factors to account for receive B1 inhomogeneity and variable coil loading, respectively. Corrections for cerebrospinal fluid content from the MRSI voxel were also applied, and the total protocol scan time was less than 15 min. The method was applied to 10 normal human volunteers using a multislice 2D-MRSI sequence at 3 T, and seven different brain regions were quantified.Results: N-Acetyl aspartate (NAA) concentrations varied from 9.7 to 14.7 mM, creatine (Cr) varied from 6.6 to 10.6 mM and choline (Cho) varied from 1.6 to 3.0 mM, in good general agreement with prior literature values.Conclusions: Quantitative SENSE-MRSI of the human brain is routinely possible using an adapted phantom-replacement technique. The method may also be applied to other MRSI techniques, including conventional phase encoding, with phased-array receiver coils, provided that coil sensitivity profiles can be measured.</description><dc:title>Quantitative SENSE-MRSI of the human brain - Corrected Proof</dc:title><dc:creator>David Bonekamp, Mari A. Smith, He Zhu, Peter B. Barker</dc:creator><dc:identifier>10.1016/j.mri.2009.11.003</dc:identifier><dc:source>Magnetic Resonance Imaging (2010)</dc:source><dc:date>2010-01-04</dc:date><prism:publicationName>Magnetic Resonance Imaging</prism:publicationName><prism:publicationDate>2010-01-04</prism:publicationDate></item></rdf:RDF>