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<title>Magnetic_Resonance_Imaging RSS : Gourt</title>
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<dc:rights>Copyright 2007, Gourt.com</dc:rights>
<dc:date>2009-11-08T02:15+27:00
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<item rdf:about="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19535208&#x26;dopt=Abstract">
<title>Improvement of spectral density-based activation detection of event-related fMRI data.</title>
<link>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19535208&#x26;dopt=Abstract</link>
<description><![CDATA[
	 Related Articles
        Improvement of spectral density-based activation detection of event-related fMRI data.
        Magn Reson Imaging. 2009 Sep;27(7):879-94
        Authors:  Ngan SC, Hu X, Tan LH, Khong PL
        For event-related data obtained from an experimental paradigm with a periodic design, spectral density at the fundamental frequency of the paradigm has been used as a template-free activation detection measure. In this article, we build and expand upon this detection measure to create an improved, integrated measure. Such an integrated measure linearly combines information contained in the spectral densities at the fundamental frequency as well as the harmonics of the paradigm and in a spatial correlation function characterizing the degree of co-activation among neighboring voxels. Several figures of merit are described and used to find appropriate values for the coefficients in the linear combination. Using receiver-operating characteristic analysis on simulated functional magnetic resonance imaging (fMRI) data sets, we quantify and validate the improved performance of the integrated measure over the spectral density measure based on the fundamental frequency as well as over some other popular template-free data analysis methods. We then demonstrate the application of the new method on an experimental fMRI data set. Finally, several extensions to this work are suggested.
        PMID: 19535208 [PubMed - indexed for MEDLINE]
    ]]></description>
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<item rdf:about="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19525079&#x26;dopt=Abstract">
<title>On MRI turbulence quantification.</title>
<link>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19525079&#x26;dopt=Abstract</link>
<description><![CDATA[
	 Related Articles
        On MRI turbulence quantification.
        Magn Reson Imaging. 2009 Sep;27(7):913-22
        Authors:  Dyverfeldt P, G&#xE5;rdhagen R, Sigfridsson A, Karlsson M, Ebbers T
        Turbulent flow, characterized by velocity fluctuations, accompanies many forms of cardiovascular disease and may contribute to their progression and hemodynamic consequences. Several studies have investigated the effects of turbulence on the magnetic resonance imaging (MRI) signal. Quantitative MRI turbulence measurements have recently been shown to have great potential for application both in human cardiovascular flow and in engineering flow. In this article, potential pitfalls and sources of error in MRI turbulence measurements are theoretically and numerically investigated. Data acquisition strategies suitable for turbulence quantification are outlined. The results show that the sensitivity of MRI turbulence measurements to intravoxel mean velocity variations is negligible, but that noise may degrade the estimates if the turbulence encoding parameter is set improperly. Different approaches for utilizing a given amount of scan time were shown to influence the dynamic range and the uncertainty in the turbulence estimates due to noise. The findings reported in this work may be valuable for both in vitro and in vivo studies employing MRI methods for turbulence quantification.
        PMID: 19525079 [PubMed - indexed for MEDLINE]
    ]]></description>
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<title>Relaxo-volumetric multispectral quantitative magnetic resonance imaging of the brain over the human lifespan: global and regional aging patterns.</title>
<link>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19520539&#x26;dopt=Abstract</link>
<description><![CDATA[
	 Related Articles
        Relaxo-volumetric multispectral quantitative magnetic resonance imaging of the brain over the human lifespan: global and regional aging patterns.
        Magn Reson Imaging. 2009 Sep;27(7):895-906
        Authors:  Saito N, Sakai O, Ozonoff A, Jara H
        The objective of this study was to determine the T1, T2 and secular-T2 relaxo-volumetric brain aging patterns using multispectral quantitative magnetic resonance imaging, both globally and regionally, and covering an age range approaching the full human lifespan. Fifty-one subjects (28 males, 23 females; age range: 0.5-87 years) were studied consisting of 18 healthy volunteers and 33 patients. Patients were selected after carefully reviewing their radiology reports to have either normal-by-MRI findings (25 patient subjects) or small focal pathology less than 6 mm in size (eight patient subjects). All subjects were MR imaged at 1.5 T with the mixed turbo spin echo pulse sequence. The soft tissues inside the cranial vault, termed intracranial matter (ICM), were segmented using a dual-clustering segmentation algorithm. ICM segments were further divided into six subsegments: bilateral anterior cerebral, posterior cerebral and cerebellar subsegments. T1, T2 and secular-T2 relaxation time histograms of all segments were generated and modeled with Gaussian functions. For each segment, the volumes of white matter, gray matter and cerebrospinal fluid were calculated from the T1 histograms. The age-related tendencies of three quantitative MRI parameters (T1, T2 and secular-T2) and the fractional tissue volumes showed four distinct periods of life, specifically a maturation period (0-2 years), a development period (2-20 years), an adulthood period (20-60 years) and a senescence period (60 years and older). For all ages, the anterior cerebral subsegment exhibited consistently longer gray matter T1s and shorter white matter T1s than the posterior cerebral and cerebellar subsegments. Volumetric age-related changes of the cerebellar subsegment were more gradual than in the cerebral subsegments. This study shows that relaxometric and volumetric age-related changes are synchronized and define the same four periods of brain evolution both globally and regionally.
        PMID: 19520539 [PubMed - indexed for MEDLINE]
    ]]></description>
</item>

<item rdf:about="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19520536&#x26;dopt=Abstract">
<title>Fast low-angle positive contrast steady-state free precession imaging of USPIO-labeled macrophages: theory and in vitro experiment.</title>
<link>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19520536&#x26;dopt=Abstract</link>
<description><![CDATA[
	 Related Articles
        Fast low-angle positive contrast steady-state free precession imaging of USPIO-labeled macrophages: theory and in vitro experiment.
        Magn Reson Imaging. 2009 Sep;27(7):961-9
        Authors:  Mascheri N, Dharmakumar R, Zhang Z, Paunesku T, Woloschak G, Li D
        The feasibility of imaging macrophages labeled with ultrasmall superparamagnetic iron-oxide nanoparticles (USPIO) with fast low-angle positive contrast steady-state free precession (FLAPS) was investigated through theory and in vitro experiment. Human macrophage cells were labeled with USPIO and imaged at 1.5 T. The metric "visibility," which combines magnitude and spatial extent of positive contrast, was used to evaluate the images. Negative contrast steady-state free precession (SSFP) and gradient-echo (GRE) imaging were also evaluated. Positive contrast was observed for relatively high concentrations of labeled cells for flip angles less than alpha=25 degrees . Theoretical and experimental results indicate that positive visibility (VIS(POS)) was maximized at alpha=10 degrees and 15 degrees. Low flip angle SSFP also provided negative contrast comparable to standard SSFP and GRE imaging. Results suggest that USPIO-labeled macrophages are capable of producing the conditions necessary for positive contrast with FLAPS at clinical field strength (1.5 T) and resolution (0.8x0.8x3 mm(3)).
        PMID: 19520536 [PubMed - indexed for MEDLINE]
    ]]></description>
</item>

<item rdf:about="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19395212&#x26;dopt=Abstract">
<title>A fully automated algorithm under modified FCM framework for improved brain MR image segmentation.</title>
<link>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19395212&#x26;dopt=Abstract</link>
<description><![CDATA[
	 Related Articles
        A fully automated algorithm under modified FCM framework for improved brain MR image segmentation.
        Magn Reson Imaging. 2009 Sep;27(7):994-1004
        Authors:  Sikka K, Sinha N, Singh PK, Mishra AK
        Automated brain magnetic resonance image (MRI) segmentation is a complex problem especially if accompanied by quality depreciating factors such as intensity inhomogeneity and noise. This article presents a new algorithm for automated segmentation of both normal and diseased brain MRI. An entropy driven homomorphic filtering technique has been employed in this work to remove the bias field. The initial cluster centers are estimated using a proposed algorithm called histogram-based local peak merger using adaptive window. Subsequently, a modified fuzzy c-mean (MFCM) technique using the neighborhood pixel considerations is applied. Finally, a new technique called neighborhood-based membership ambiguity correction (NMAC) has been used for smoothing the boundaries between different tissue classes as well as to remove small pixel level noise, which appear as misclassified pixels even after the MFCM approach. NMAC leads to much sharper boundaries between tissues and, hence, has been found to be highly effective in prominently estimating the tissue and tumor areas in a brain MR scan. The algorithm has been validated against MFCM and FMRIB software library using MRI scans from BrainWeb. Superior results to those achieved with MFCM technique have been observed along with the collateral advantages of fully automatic segmentation, faster computation and faster convergence of the objective function.
        PMID: 19395212 [PubMed - indexed for MEDLINE]
    ]]></description>
</item>

<item rdf:about="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19369023&#x26;dopt=Abstract">
<title>Image correction during large and rapid B(0) variations in an open MRI system with permanent magnets using navigator echoes and phase compensation.</title>
<link>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19369023&#x26;dopt=Abstract</link>
<description><![CDATA[
	 Related Articles
        Image correction during large and rapid B(0) variations in an open MRI system with permanent magnets using navigator echoes and phase compensation.
        Magn Reson Imaging. 2009 Sep;27(7):988-93
        Authors:  Li J, Wang Y, Jiang Y, Xie H, Li G
        An open permanent magnet system with vertical B(0) field and without self-shielding can be quite susceptible to perturbations from external magnetic sources. B(0) variation in such a system located close to a subway station was measured to be greater than 0.7 microT by both MRI and a fluxgate magnetometer. This B(0) variation caused image artifacts. A navigator echo approach that monitored and compensated the view-to-view variation in magnetic resonance signal phase was developed to correct for image artifacts. Human brain imaging experiments using a multislice gradient-echo sequence demonstrated that the ghosting and blurring artifacts associated with B(0) variations were effectively removed using the navigator method.
        PMID: 19369023 [PubMed - indexed for MEDLINE]
    ]]></description>
</item>

<item rdf:about="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19369022&#x26;dopt=Abstract">
<title>Magnetic resonance imaging tracking of alginate beads used for drug delivery of growth factors at sites of cardiac damage.</title>
<link>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19369022&#x26;dopt=Abstract</link>
<description><![CDATA[
	 Related Articles
        Magnetic resonance imaging tracking of alginate beads used for drug delivery of growth factors at sites of cardiac damage.
        Magn Reson Imaging. 2009 Sep;27(7):970-5
        Authors:  Gruwel ML, Yang Y, de Gervai P, Sun J, Kupriyanov VV
        Alginate-based beads labeled with contrast agent and loaded with vascular growth hormones were used for site-specific chronic delivery of hormones at the site of myocardial damage in a porcine model. Position of the beads within the pericardium could be monitored by MRI for optimal hormone delivery due to the presence of contrast agent. The beads facilitate the slow release of cytochrome c, myoglobin and methemoglobin used as protein models of growth factors. This application allows for site-specific delivery of hormones while the incorporated contrast agent in the beads provides a tool for MRI tracking in chronic studies.
        PMID: 19369022 [PubMed - indexed for MEDLINE]
    ]]></description>
</item>

<item rdf:about="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19369021&#x26;dopt=Abstract">
<title>A nonlinear BOLD model accounting for refractory effect by applying the longitudinal relaxation in NMR to the linear BOLD model.</title>
<link>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19369021&#x26;dopt=Abstract</link>
<description><![CDATA[
	 Related Articles
        A nonlinear BOLD model accounting for refractory effect by applying the longitudinal relaxation in NMR to the linear BOLD model.
        Magn Reson Imaging. 2009 Sep;27(7):907-12
        Authors:  Jung KJ
        A mathematical model to regress the nonlinear blood oxygen level-dependent (BOLD) fMRI signal has been developed by incorporating the refractory effect into the linear BOLD model of the biphasic gamma variate function. The refractory effect was modeled as a relaxation of two separate BOLD capacities corresponding to the biphasic components of the BOLD signal in analogy with longitudinal relaxation of magnetization in NMR. When tested with the published fMRI data of finger tapping, the nonlinear BOLD model with the refractory effect reproduced the nonlinear BOLD effects such as reduced poststimulus undershoot and saddle pattern in a prolonged stimulation as well as the reduced BOLD signal for repetitive stimulation.
        PMID: 19369021 [PubMed - indexed for MEDLINE]
    ]]></description>
</item>

<item rdf:about="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19369020&#x26;dopt=Abstract">
<title>Acute pancreatic graft fistula and peripancreatic fluid collection: demonstration by secretin-stimulated MRI.</title>
<link>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19369020&#x26;dopt=Abstract</link>
<description><![CDATA[
	 Related Articles
        Acute pancreatic graft fistula and peripancreatic fluid collection: demonstration by secretin-stimulated MRI.
        Magn Reson Imaging. 2009 Sep;27(7):1005-8
        Authors:  Alkaade S, Fattahi R, Balci NC, Akduman EI, Garvin PJ, Modanlou KA, Burton FR
        Peripancreatic fluid collections are among the common post pancreas transplant complications, which are mainly due to leakage from the anastomosis site to bowel and graft pancreatitis. Differentiation between these two entities is important because they are treated differently. In this case, secretin stimulated magnetic resonance cholangiopancreatography revealed gradual intraperitoneal fluid collection and accumulation of fluid in small bowel excluded leakage from the anastomosis of the pancreas to bowel and changed the management from surgery to medical treatment.
        PMID: 19369020 [PubMed - indexed for MEDLINE]
    ]]></description>
</item>

<item rdf:about="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19356874&#x26;dopt=Abstract">
<title>MRI findings in nonalcoholic steatohepatitis: correlation with histopathology and clinical staging.</title>
<link>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19356874&#x26;dopt=Abstract</link>
<description><![CDATA[
	 Related Articles
        MRI findings in nonalcoholic steatohepatitis: correlation with histopathology and clinical staging.
        Magn Reson Imaging. 2009 Sep;27(7):976-87
        Authors:  Elias J, Altun E, Zacks S, Armao DM, Woosley JT, Semelka RC
        PURPOSE: To evaluate magnetic resonance imaging (MRI) findings of nonalcoholic steatohepatitis (NASH) and to determine the correlation of MRI findings with histopathology and Mayo End-Stage Liver Disease (MELD) score. MATERIALS AND METHODS: Thirty patients (18 males, 12 females; mean age: 57+/-8.9 years; age range: 35-71 years) with histopathologically proven NASH who underwent MRI examinations between January 2001 and October 2005 were included in the study. Two radiologists retrospectively reviewed all magnetic resonance (MR) examinations in consensus to evaluate the presence and extent of predetermined findings of NASH including liver steatosis, early patchy liver enhancement indicating inflammation and liver fibrosis. The findings detected on MRI were correlated and compared to histopathological findings and MELD score by using nonparametric Spearman correlation coefficient and Kruskal-Wallis analysis of variance. RESULTS: Liver steatosis was observed in 10 of 30 patients; early patchy liver enhancement, in 8 of 30 patients and liver fibrosis in 19 of 30 patients on MR images. Liver fibrosis was reticular in all these patients. There were statistically significant moderate correlations between MRI findings of liver steatosis and histopathologic grades of steatosis (r=0.43; P&lt;.05), and between MRI findings of fibrosis and histopathologic stages of fibrosis (r=0.61; P&lt;.001). Early patchy enhancement did not demonstrate statistically significant correlation with inflammation (P=.28). There was no statistically significant overall correlation between MRI findings of NASH and MELD score. CONCLUSION: MRI findings of liver steatosis and fibrosis in NASH showed moderate correlations with histopathologic grades of steatosis and stages of fibrosis, but MRI findings of NASH did not demonstrate any significant correlations with MELD score.
        PMID: 19356874 [PubMed - indexed for MEDLINE]
    ]]></description>
</item>

<item rdf:about="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19286338&#x26;dopt=Abstract">
<title>Improved SNR in linear reordered 2D bSSFP imaging using variable flip angles.</title>
<link>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19286338&#x26;dopt=Abstract</link>
<description><![CDATA[
	 Related Articles
        Improved SNR in linear reordered 2D bSSFP imaging using variable flip angles.
        Magn Reson Imaging. 2009 Sep;27(7):933-41
        Authors:  Paul D, Zaitsev M
        This article presents a variable flip-angle approach for balanced steady-state free precession (bSSFP) imaging, which allows increases in signal-to-noise ratio (SNR) and contrast-to-noise ratio (CNR) while keeping specific absorption rate (SAR) constant or reduces SAR for given CNR and SNR. The gain in SNR is achieved by utilizing the higher signal in the transient phase. Flip-angle variation during the echo train is realized using a trigonometric function with M steps (ramp length). Variation is combined with a linear k-space reordering such that outer parts of k-space are sampled using a lower flip angle alpha(min), while the central part of k-space is acquired with a higher flip angle alpha(max). No additional preparation or dummy cycles are applied prior to data acquisition. Several variation schemes with different starting flip angles alpha(min) and ramp length M are considered. For example, using alpha(min)=1 degrees and M=96, alpha(max) can be set to 47 degrees without exceeding SAR limits at 3 T and gaining up to 50% in SNR, while, conventionally, alpha=34 degrees is the maximal possible flip angle. Resolution seems unaffected in volunteer imaging. In all cases, no transient artifacts due to flip-angle variation were observed. This article demonstrates the use of flip-angle variations in bSSFP to increase SNR and CNR while keeping SAR constant, which is especially important at higher field strengths. Flip-angle variation can also be combined with other methods such as parallel imaging techniques for further SAR reduction.
        PMID: 19286338 [PubMed - indexed for MEDLINE]
    ]]></description>
</item>

<item rdf:about="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19282122&#x26;dopt=Abstract">
<title>Noninvasive monitoring of brain temperature during mild hypothermia.</title>
<link>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19282122&#x26;dopt=Abstract</link>
<description><![CDATA[
	 Related Articles
        Noninvasive monitoring of brain temperature during mild hypothermia.
        Magn Reson Imaging. 2009 Sep;27(7):923-32
        Authors:  Weis J, Covaciu L, Rubertsson S, Allers M, Lunderquist A, Ahlstr&#xF6;m H
        The main purpose of this study was to verify the feasibility of brain temperature mapping with high-spatial- and reduced-spectral-resolution magnetic resonance spectroscopic imaging (MRSI). A secondary goal was to determine the temperature coefficient of water chemical shift in the brain with and without internal spectral reference. The accuracy of the proposed MRSI method was verified using a water and vegetable oil phantom. Selective decrease of the brain temperature of pigs was induced by intranasal cooling. Temperature reductions between 2 degrees C and 4 degrees C were achieved within 20 min. The relative changes in temperature during the cooling process were monitored using MRSI. The reference temperature was measured with MR-compatible fiber-optic probes. Single-voxel (1)H MRS was used for measurement of absolute brain temperature at baseline and at the end of cooling. The temperature coefficient of the water chemical shift of brain tissue measured by MRSI without internal reference was -0.0192+/-0.0019 ppm/degrees C. The temperature coefficients of the water chemical shift relative to N-acetylaspartate, choline-containing compounds and creatine were -0.0096+/-0.0009, -0.0083+/-0.0007 and -0.0091+/-0.0011 ppm/degrees C, respectively. The results of this study indicate that MRSI with high spatial and reduced spectral resolutions is a reliable tool for monitoring long-term temperature changes in the brain.
        PMID: 19282122 [PubMed - indexed for MEDLINE]
    ]]></description>
</item>

<item rdf:about="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19282121&#x26;dopt=Abstract">
<title>Assessment of the internal craniocervical ligaments with a new magnetic resonance imaging sequence: three-dimensional turbo spin echo with variable flip-angle distribution (SPACE).</title>
<link>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19282121&#x26;dopt=Abstract</link>
<description><![CDATA[
	 Related Articles
        Assessment of the internal craniocervical ligaments with a new magnetic resonance imaging sequence: three-dimensional turbo spin echo with variable flip-angle distribution (SPACE).
        Magn Reson Imaging. 2009 Sep;27(7):954-60
        Authors:  Baumert B, W&#xF6;rtler K, Steffinger D, Schmidt GP, Reiser MF, Baur-Melnyk A
        PURPOSE: Lesions close to the internal craniocervical ligaments are a common problem in patients with whiplash injuries. The aim of this study was to evaluate the morphology and visibility of these ligamentous structures with a new isotropic three-dimensional (3D) turbo-spin-echo (TSE) technique. MATERIALS AND METHODS: MR (MR) images of the cervical spine of 52 healthy subjects (27 women and 25 men; mean age=29 years; age range=18-40 years) were taken with a T2-weighted 3D TSE sequence with variable flip-angle distribution [SPACE (Sampling Perfection with Application optimized Contrasts using different flip-angle Evolution)] at 1.5 T (Magnetom Avanto, Siemens Erlangen, Germany). Two experienced musculoskeletal radiologists read the images independently on a 3D imaging and postprocessing workstation. The visibility and morphology of the alar ligaments were evaluated on a five-point scale, and inter-reader correlation was assessed with kappa statistics. RESULTS: Both alar ligaments were detected in all subjects. Twenty-eight (53.8%) of the alar ligaments could not be seen within one slice of the standard coronal imaging plane but could adequately be visualized in an oblique reconstruction adapted to the orientation of the ligaments on the axial slices. Inter-reader correlation for visibility on MR imaging (MRI) of the internal craniocervical ligaments was high (left+right side, kappa=0.95). Most (94%) alar ligaments presented symmetrically. In the axial plane, 60% were oriented neutral and 40% had a backward orientation. In the coronal plane, 67% were oriented caudocranially and 33% were oriented horizontally. The shape of the ligaments was parallel in half and was V-shaped in the other half. The alar ligaments had homogeneous low-signal intensity in 56% and heterogeneous low-signal intensity in 44%. The apical ligament of the dens was seen (excellent-good-moderate) in 61% (reader 1) and 52% (reader 2). The tectorial membranes and the transverse ligament of the atlas were shown (excellent-good) in all subjects. CONCLUSIONS: MRI with acquisition of an isotropic SPACE technique allows high-resolution imaging of the craniocervical ligaments in all orientations. Reconstruction of the image data in the variable orientation of the alar ligaments allowed for excellent depiction within one slice such that partial volume artifacts that hamper image analysis can be eliminated.
        PMID: 19282121 [PubMed - indexed for MEDLINE]
    ]]></description>
</item>

<item rdf:about="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19269768&#x26;dopt=Abstract">
<title>Improved matrix inversion in image plane parallel MRI.</title>
<link>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19269768&#x26;dopt=Abstract</link>
<description><![CDATA[
	 Related Articles
        Improved matrix inversion in image plane parallel MRI.
        Magn Reson Imaging. 2009 Sep;27(7):942-53
        Authors:  Wu B, Millane RP, Watts R, Bones PJ
        A new 3D parallel magnetic resonance imaging (MRI) method named Generalized Unaliasing Incorporating Support constraint and sensitivity Encoding (GUISE) is presented. GUISE allows direct image recovery from arbitrary Cartesian k-space trajectories. However, periodic k-space sampling patterns are considered for reconstruction efficiency. Image recovery methods such as 2D SENSE (SENSitivity Encoding) and 2D CAIPIRINHA (Controlled Aliasing In Parallel Imaging Results IN Higher Acceleration) are special instances of GUISE where specific restrictions are placed on the k-space sampling patterns used. It is shown that the sampling pattern has large impacts on the image reconstruction error due to noise. An efficient sampling pattern design method that incorporates prior knowledge of object support and coil sensitivity profile is proposed. It requires no experimental trials and could be used in clinical imaging. Comparison of the proposed sampling pattern design method with 2D SENSE and 2D CAIPIRINHA are made based on both simulation and experiment results. It is seen that this new adaptive sampling pattern design method results in a lower noise level in reconstructions due to better exploitation of the coil sensitivity variation and object support constraint. In addition, elimination of the non-object region from reconstruction potentially allows an acceleration factor higher than the number of receiver coils used.
        PMID: 19269768 [PubMed - indexed for MEDLINE]
    ]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22142">
<title>3D noncontrast MR angiography of the distal lower extremities using flow-sensitive dephasing (FSD)-prepared balanced SSFP</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22142</link>
<description><![CDATA[While three-dimensional contrast-enhanced MR angiography (MRA) is becoming the method of choice for clinical peripheral arterial disease (PAD) examinations, safety concerns with contrast administration in patients with renal insufficiency have triggered a renaissance of noncontrast MRA. In this work, a noncontrast-MRA technique using electrocardiography-triggered three-dimensional segmented balanced steady-state free precession with flow-sensitive dephasing (FSD) magnetization preparation was developed and tested in the distal lower extremities. FSD preparation was used to induce arterial flow voids at systolic cardiac phase while having little effect on venous blood and static tissues. High-spatial-resolution MRA was obtained by means of magnitude subtraction between a dark-artery scan with FSD preparation at systole and a bright-artery scan without FSD preparation at mid-diastole. In nine healthy volunteers, FSD parameters, including the gradient waveform and the first-order gradient moment, were optimized for excellent MRA image quality. Furthermore, arterial stenosis and occlusion in two peripheral arterial disease patients were identified using the noncontrast-MRA technique, as confirmed by contrast-enhanced MRA. In conclusion, FSD-prepared balanced steady-state free precession in conjunction with electrocardiography gating and image subtraction provides a promising noncontrast-MRA strategy for the distal lower extremities. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22100">
<title>Characterizing and correcting gradient errors in non-cartesian imaging: Are gradient errors linear time-invariant (LTI)?</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22100</link>
<description><![CDATA[Non-Cartesian and rapid imaging sequences are more sensitive to scanner imperfections such as gradient delays and eddy currents. These imperfections vary between scanners and over time and can be a significant impediment to successful implementation and eventual adoption of non-Cartesian techniques by scanner manufacturers. Differences between the k-space trajectory desired and the trajectory actually acquired lead to misregistration and reduction in image quality. While early calibration methods required considerable scan time, more recent methods can work more quickly by making certain approximations. We examine a rapid gradient calibration procedure applied to multiecho three-dimensional projection reconstruction (3DPR) acquisitions in which the calibration runs as part of every scan. After measuring the trajectories traversed for excitations on each of the orthogonal gradient axes, trajectories for the oblique projections actually acquired during the scan are synthesized as linear combinations of these measurements. The ability to do rapid calibration depends on the assumption that gradient errors are linear and time-invariant (LTI). This work examines the validity of these assumptions and shows that the assumption of linearity is reasonable, but that gradient errors can vary over short time periods (due to changes in gradient coil temperature) and thus it is important to use calibration data matched to the scan data. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22122">
<title>Robust GRAPPA-accelerated diffusion-weighted readout-segmented (RS)-EPI</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22122</link>
<description><![CDATA[Readout segmentation (RS-EPI) has been suggested as a promising variant to echo-planar imaging (EPI) for high-resolution imaging, particularly when combined with parallel imaging. This work details some of the technical aspects of diffusion-weighted (DW)-RS-EPI, outlining a set of reconstruction methods and imaging parameters that can both minimize the scan time and afford high-resolution diffusion imaging with reduced distortions. These methods include an efficient generalized autocalibrating partially parallel acquisition (GRAPPA) calibration for DW-RS-EPI data without scan time penalty, together with a variant for the phase correction of partial Fourier RS-EPI data. In addition, the role of pulsatile and rigid-body brain motion in DW-RS-EPI was assessed. Corrupt DW-RS-EPI data arising from pulsatile nonlinear brain motion had a prevalence of [sim]7% and were robustly identified via k-space entropy metrics. For DW-RS-EPI data corrupted by rigid-body motion, we showed that no blind overlap was required. The robustness of RS-EPI toward phase errors and motion, together with its minimized distortions compared with EPI, enables the acquisition of exquisite 3 T DW images with matrix sizes close to 5122. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22145">
<title>Investigation and modeling of magnetization transfer effects in two-dimensional multislice turbo spin echo sequences with low constant or variable flip angles at 3 T</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22145</link>
<description><![CDATA[Magnetization transfer effects represent a major source of contrast in multislice turbo spin echo sequences (TSE)/fast spin echo sequences. Generally, low refocusing flip angles have become common in such MRI sequences, especially to mitigate specific absorption rate problems. Since the strength of magnetization transfer effects is related to the radiofrequency power and therefore specific absorption rate applied, magnetization transfer induced signal attenuations are investigated for a variety of TSE sequences with low constant and variable flip angles. Noticeable differences between the sequences have been observed. In particular, fewer signal attenuations are observed for TSE with low flip angles such as hyperecho-TSE and smooth transitions between pseudo steady states-TSE, leading to contrast that is less dependent on the number of slices. It is shown that the strength of the magnetization transfer-induced signal attenuations can be understood and described by a physical framework, which is based on the mean square flip angle of a given TSE sequence. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22219">
<title>A 2D MTF approach to evaluate and guide dynamic imaging developments</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22219</link>
<description><![CDATA[As the number and complexity of partially sampled dynamic imaging methods continue to increase, reliable strategies to evaluate performance may prove most useful. In the present work, an analytical framework to evaluate given reconstruction methods is presented. A perturbation algorithm allows the proposed evaluation scheme to perform robustly without requiring knowledge about the inner workings of the method being evaluated. A main output of the evaluation process consists of a two-dimensional modulation transfer function, an easy-to-interpret visual rendering of a method's ability to capture all combinations of spatial and temporal frequencies. Approaches to evaluate noise properties and artifact content at all spatial and temporal frequencies are also proposed. One fully sampled phantom and three fully sampled cardiac cine datasets were subsampled (R = 4 and 8) and reconstructed with the different methods tested here. A hybrid method, which combines the main advantageous features observed in our assessments, was proposed and tested in a cardiac cine application, with acceleration factors of 3.5 and 6.3 (skip factors of 4 and 8, respectively). This approach combines features from methods such as k-t sensitivity encoding, unaliasing by Fourier encoding the overlaps in the temporal dimension-sensitivity encoding, generalized autocalibrating partially parallel acquisition, sensitivity profiles from an array of coils for encoding and reconstruction in parallel, self, hybrid referencing with unaliasing by Fourier encoding the overlaps in the temporal dimension and generalized autocalibrating partially parallel acquisition, and generalized autocalibrating partially parallel acquisition-enhanced sensitivity maps for sensitivity encoding reconstructions. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22168">
<title>Initial results on in vivo human coronary MR angiography at 7 T</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22168</link>
<description><![CDATA[Seven tesla (T) MR imaging is potentially promising for the morphologic evaluation of coronary arteries because of the increased signal-to-noise ratio compared to lower field strengths, in turn allowing improved spatial resolution, improved temporal resolution, or reduced scanning times. However, there are a large number of technical challenges, including the commercial 7 T systems not being equipped with homogeneous body radiofrequency coils, conservative specific absorption rate constraints, and magnified sample-induced amplitude of radiofrequency field inhomogeneity. In the present study, an initial attempt was made to address these challenges and to implement coronary MR angiography at 7 T. A single-element radiofrequency transmit and receive coil was designed and a 7 T specific imaging protocol was implemented, including significant changes in scout scanning, contrast generation, and navigator geometry compared to current protocols at 3 T. With this methodology, the first human coronary MR images were successfully obtained at 7 T, with both qualitative and quantitative findings being presented. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22167">
<title>Tailored RF pulse for magnetization inversion at ultrahigh field</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22167</link>
<description><![CDATA[The radiofrequency (RF) transmit field is severely inhomogeneous at ultrahigh field due to both RF penetration and RF coil design issues. This particularly impairs image quality for sequences that use inversion pulses such as magnetization prepared rapid acquisition gradient echo and limits the use of quantitative arterial spin labeling sequences such as flow-attenuated inversion recovery. Here we have used a search algorithm to produce inversion pulses tailored to take into account the heterogeneity of the RF transmit field at 7 T. This created a slice selective inversion pulse that worked well (good slice profile and uniform inversion) over the range of RF amplitudes typically obtained in the head at 7 T while still maintaining an experimentally achievable pulse length and pulse amplitude in the brain at 7 T. The pulses used were based on the frequency offset correction inversion technique, as well as time dilation of functions, but the RF amplitude, frequency sweep, and gradient functions were all generated using a genetic algorithm with an evaluation function that took into account both the desired inversion profile and the transmit field inhomogeneity. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22166">
<title>Delayed gadolinium-enhanced magnetic resonance imaging (dGEMRIC) of hip joint cartilage in femoroacetabular impingement (FAI): Are pre- and postcontrast imaging both necessary?</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22166</link>
<description><![CDATA[The purpose of this study was to assess if delayed gadolinium MRI of cartilage using postcontrast T1 (T1Gd) is sufficient for evaluating cartilage damage in femoroacetabular impingement without using noncontrast values (T10). T1Gd and [Delta]R1 (1/T1Gd - 1/T10) that include noncontrast T1 measurements were studied in two grades of osteoarthritis and in a control group of asymptomatic young-adult volunteers. Differences between T1Gd and [Delta]R1 values for femoroacetabular impingement patients and volunteers were compared. There was a very high correlation between T1Gd and [Delta]R1 in all study groups. In the study cohort with Tonnis grade 0, correlation (r) was -0.95 and -0.89 with Tonnis grade 1 and -0.88 in asymptomatic volunteers, being statistically significant (P < 0.001) for all groups. For both T1Gd and [Delta]R1, a statistically significant difference was noted between patients and control group. Significant difference was also noted for both T1Gd and [Delta]R1 between the patients with Tonnis grade 0 osteoarthritis and those with grade 1 changes. Our results prove a linear correlation between T1Gd and [Delta]R1, suggesting that T1Gd assessment is sufficient for the clinical utility of delayed gadolinium MRI of cartilage in this setting and additional time-consuming T10 evaluation may not be needed. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22159">
<title>Disease state prediction from resting state functional connectivity</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22159</link>
<description><![CDATA[The application of multivoxel pattern analysis methods has attracted increasing attention, particularly for brain state prediction and real-time functional MRI applications. Support vector classification is the most popular of these techniques, owing to reports that it has better prediction accuracy and is less sensitive to noise. Support vector classification was applied to learn functional connectivity patterns that distinguish patients with depression from healthy volunteers. In addition, two feature selection algorithms were implemented (one filter method, one wrapper method) that incorporate reliability information into the feature selection process. These reliability feature selections methods were compared to two previously proposed feature selection methods. A support vector classifier was trained that reliably distinguishes healthy volunteers from clinically depressed patients. The reliability feature selection methods outperformed previously utilized methods. The proposed framework for applying support vector classification to functional connectivity data is applicable to other disease states beyond major depression. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22178">
<title>T2 measurement in articular cartilage: Impact of the fitting method on accuracy and precision at low SNR</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22178</link>
<description><![CDATA[T2 relaxation time is a promising MRI parameter for the detection of cartilage degeneration in osteoarthritis. However, the accuracy and precision of the measured T2 may be substantially impaired by the low signal-to-noise ratio of images available from clinical examinations. The purpose of this work was to assess the accuracy and precision of the traditional fit methods (linear least-squares regression and nonlinear fit to an exponential) and two new noise-corrected fit methods: fit to a noise-corrected exponential and fit of the noise-corrected squared signal intensity to an exponential. Accuracy and precision have been analyzed in simulations, in phantom measurements, and in seven repetitive acquisitions of the patellar cartilage in six healthy volunteers. Traditional fit methods lead to a poor accuracy for low T2, with overestimations of the exact T2 up to 500%. The noise-corrected fit methods demonstrate a very good accuracy for all T2 values and signal-to-noise ratio. Even more, the fit to a noise-corrected exponential results in precisions comparable to the best achievable precisions (Cramér-Rao lower bound). For in vivo images, the traditional fit methods considerably overestimate T2 near the bone-cartilage interface. Therefore, using an adequate fit method may substantially improve the sensitivity of T2 to detect pathology in cartilage and change in T2 follow-up examinations. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22197">
<title>IIR GRAPPA for parallel MR image reconstruction</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22197</link>
<description><![CDATA[Accelerated parallel MRI has advantage in imaging speed, and its image quality has been improved continuously in recent years. This paper introduces a two-dimensional infinite impulse response model of inverse filter to replace the finite impulse response model currently used in generalized autocalibrating partially parallel acquisitions class image reconstruction methods. The infinite impulse response model better characterizes the correlation of k-space data points and better approximates the perfect inversion of parallel imaging process, resulting in a novel generalized image reconstruction method for accelerated parallel MRI. This k-space-based reconstruction method includes the conventional generalized autocalibrating partially parallel acquisitions class methods as special cases and has a new infinite impulse response data estimation mechanism for effective improvement of image quality. The experiments on in vivo MRI data show that the proposed method significantly reduces reconstruction errors compared with the conventional two-dimensional generalized autocalibrating partially parallel acquisitions method, particularly at the high acceleration rates. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22186">
<title>Improved technique for measurement of regional fractional ventilation by hyperpolarized 3He MRI</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22186</link>
<description><![CDATA[Quantitative measurement of regional lung ventilation is of great significance in assessment of lung function in many obstructive and restrictive pulmonary diseases. A new technique for regional measurement of fractional ventilation using hyperpolarized 3He MRI is proposed, addressing the shortcomings of an earlier approach that limited its use to small animals. The new approach allows for the acquisition of similar quantitative maps over a shortened period and requires substantially less 3He gas. This technique is therefore a better platform for implementation in large species, including humans. The measurements using the two approaches were comparable to a great degree, as verified in a healthy rat lung, and are very reproducible. Preliminary validation is performed in a lung phantom system. Volume dependency of measurements was assessed both in vivo and in vitro. A scheme for selecting an optimum flip angle is proposed. In addition, a dead space modeling approach is proposed to yield more accurate measurements of regional fractional ventilation using either method. Finally, sensitivity of the new technique to model parameters, noise, and number of included images were assessed numerically. As a prelude to application in humans, the technique was implemented in a large animal study successfully. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22183">
<title>3D steady-state diffusion-weighted imaging with trajectory using radially batched internal navigator echoes (TURBINE)</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22183</link>
<description><![CDATA[While most diffusion-weighted imaging (DWI) is acquired using single-shot diffusion-weighted spin-echo echo-planar imaging, steady-state DWI is an alternative method with the potential to achieve higher-resolution images with less distortion. Steady-state DWI is, however, best suited to a segmented three-dimensional acquisition and thus requires three-dimensional navigation to fully correct for motion artifacts. In this paper, a method for three-dimensional motion-corrected steady-state DWI is presented. The method uses a unique acquisition and reconstruction scheme named trajectory using radially batched internal navigator echoes (TURBINE). Steady-state DWI with TURBINE uses slab-selection and a short echo-planar imaging (EPI) readout each pulse repetition time. Successive EPI readouts are rotated about the phase-encode axis. For image reconstruction, batches of cardiac-synchronized readouts are used to form three-dimensional navigators from a fully sampled central k-space cylinder. In vivo steady-state DWI with TURBINE is demonstrated in human brain. Motion artifacts are corrected using refocusing reconstruction and TURBINE images prove less distorted compared to two-dimensional single-shot diffusion-weighted-spin-EPI. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22180">
<title>Optimization of k-space trajectories for compressed sensing by Bayesian experimental design</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22180</link>
<description><![CDATA[The optimization of k-space sampling for nonlinear sparse MRI reconstruction is phrased as a Bayesian experimental design problem. Bayesian inference is approximated by a novel relaxation to standard signal processing primitives, resulting in an efficient optimization algorithm for Cartesian and spiral trajectories. On clinical resolution brain image data from a Siemens 3T scanner, automatically optimized trajectories lead to significantly improved images, compared to standard low-pass, equispaced, or variable density randomized designs. Insights into the nonlinear design optimization problem for MRI are given. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22177">
<title>Robust water/fat separation in the presence of large field inhomogeneities using a graph cut algorithm</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22177</link>
<description><![CDATA[Water/fat separation is a classical problem for in vivo proton MRI. Although many methods have been proposed to address this problem, robust water/fat separation remains a challenge, especially in the presence of large amplitude of static field inhomogeneities. This problem is challenging because of the nonuniqueness of the solution for an isolated voxel. This paper tackles the problem using a statistically motivated formulation that jointly estimates the complete field map and the entire water/fat images. This formulation results in a difficult optimization problem that is solved effectively using a novel graph cut algorithm, based on an iterative process where all voxels are updated simultaneously. The proposed method has good theoretical properties, as well as an efficient implementation. Simulations and in vivo results are shown to highlight the properties of the proposed method and compare it to previous approaches. Twenty-five cardiac datasets acquired on a short, wide-bore scanner with different slice orientations were used to test the proposed method, which produced robust water/fat separation for these challenging datasets. This paper also shows example applications of the proposed method, such as the characterization of intramyocardial fat. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22173">
<title>Quantitative T2 analysis: The effects of noise, regularization, and multivoxel approaches</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22173</link>
<description><![CDATA[Typical quantitative T2 (qT2) analysis involves creating T2 distributions using a regularized algorithm from region-of-interest averaged decay data. This study uses qT2 analysis of simulated and experimental decay signals to determine how (a) noise-type, (b) regularization, and (c) region-of-interest versus multivoxel analyses affect T2 distributions. Our simulations indicate that regularization causes myelin water fraction and intra/extracellular water geometric mean T2 underestimation that worsens as the signal-to-noise ratio decreases. The underestimation was greater for intra/extracellular water geometric mean T2 measures using Rician noise. Simulations showed significant differences between myelin water fractions determined using region-of-interest and multivoxel approaches compared to the true value. The nonregularized voxel-based approach gave the most accurate measure of myelin water fraction and intra/extracellular water geometric mean T2 for a given signal-to-noise ratio and noise type. Additionally, multivoxel analysis provides important information about the variability of the analysis. Results obtained from in vivo rat data were similar to our simulation results. In each case, a nonregularized, multivoxel analysis provided myelin water fractions significantly different from the regularized approaches and obtained the largest myelin water fraction. We conclude that quantitative T2 analysis is best performed using a nonregularized, multivoxel approach. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22172">
<title>Radial k-t FOCUSS for high-resolution cardiac cine MRI</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22172</link>
<description><![CDATA[A compressed sensing dynamic MR technique called k-t FOCUSS (k-t FOCal Underdetermined System Solver) has been recently proposed. It outperforms the conventional k-t BLAST/SENSE (Broad-use Linear Acquisition Speed-up Technique/SENSitivity Encoding) technique by exploiting the sparsity of x-f signals. This paper applies this idea to radial trajectories for high-resolution cardiac cine imaging. Radial trajectories are more suitable for high-resolution dynamic MRI than Cartesian trajectories since there is smaller tradeoff between spatial resolution and number of views if streaking artifacts due to limited views can be resolved. As shown for Cartesian trajectories, k-t FOCUSS algorithm efficiently removes artifacts while preserving high temporal resolution. k-t FOCUSS algorithm applied to radial trajectories is expected to enhance dynamic MRI quality. Rather than using an explicit gridding method, which transforms radial k-space sampling data to Cartesian grid prior to applying k-t FOCUSS algorithms, we use implicit gridding during FOCUSS iterations to prevent k-space sampling errors from being propagated. In addition, motion estimation and motion compensation after the first FOCUSS iteration were used to further sparsify the residual image. By applying an additional k-t FOCUSS step to the residual image, improved resolution was achieved. In vivo experimental results show that this new method can provide high spatiotemporal resolution even from a very limited radial data set. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22170">
<title>Reconstruction from free-breathing cardiac MRI data using reproducing kernel Hilbert spaces</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22170</link>
<description><![CDATA[This paper describes a rigorous framework for reconstructing MR images of the heart, acquired continuously over the cardiac and respiratory cycle. The framework generalizes existing techniques, commonly referred to as retrospective gating, and is based on the properties of reproducing kernel Hilbert spaces. The reconstruction problem is formulated as a moment problem in a multidimensional reproducing kernel Hilbert spaces (a two-dimensional space for cardiac and respiratory resolved imaging). Several reproducing kernel Hilbert spaces were tested and compared, including those corresponding to commonly used interpolation techniques (sinc-based and splines kernels) and a more specific kernel allowed by the framework (based on a first-order Sobolev RKHS). The Sobolev reproducing kernel Hilbert spaces was shown to allow improved reconstructions in both simulated and real data from healthy volunteers, acquired in free breathing. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22157">
<title>Sodium MRI using a density-adapted 3D radial acquisition technique</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22157</link>
<description><![CDATA[A density-adapted three-dimensional radial projection reconstruction pulse sequence is presented which provides a more efficient k-space sampling than conventional three-dimensional projection reconstruction sequences. The gradients of the density-adapted three-dimensional radial projection reconstruction pulse sequence are designed such that the averaged sampling density in each spherical shell of k-space is constant. Due to hardware restrictions, an inner sphere of k-space is sampled without density adaption. This approach benefits from both the straightforward handling of conventional three-dimensional projection reconstruction sequence trajectories and an enhanced signal-to-noise ratio (SNR) efficiency akin to the commonly used three-dimensional twisted projection imaging trajectories. Benefits for low SNR applications, when compared to conventional three-dimensional projection reconstruction sequences, are demonstrated with the example of sodium imaging. In simulations of the point-spread function, the SNR of small objects is increased by a factor 1.66 for the density-adapted three-dimensional radial projection reconstruction pulse sequence sequence. Using analytical and experimental phantoms, it is shown that the density-adapted three-dimensional radial projection reconstruction pulse sequence allows higher resolutions and is more robust in the presence of field inhomogeneities. High-quality in vivo images of the healthy human leg muscle and the healthy human brain are acquired. For equivalent scan times, the SNR is up to a factor of 1.8 higher and anatomic details are better resolved using density-adapted three-dimensional radial projection reconstruction pulse sequence. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22147">
<title>Classification of brain tumor type and grade using MRI texture and shape in a machine learning scheme</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22147</link>
<description><![CDATA[The objective of this study is to investigate the use of pattern classification methods for distinguishing different types of brain tumors, such as primary gliomas from metastases, and also for grading of gliomas. The availability of an automated computer analysis tool that is more objective than human readers can potentially lead to more reliable and reproducible brain tumor diagnostic procedures. A computer-assisted classification method combining conventional MRI and perfusion MRI is developed and used for differential diagnosis. The proposed scheme consists of several steps including region-of-interest definition, feature extraction, feature selection, and classification. The extracted features include tumor shape and intensity characteristics, as well as rotation invariant texture features. Feature subset selection is performed using support vector machines with recursive feature elimination. The method was applied on a population of 102 brain tumors histologically diagnosed as metastasis (), meningiomas (), gliomas World Health Organization grade II (), gliomas World Health Organization grade III (), and glioblastomas (). The binary support vector machine classification accuracy, sensitivity, and specificity, assessed by leave-one-out cross-validation, were, respectively, 85%, 87%, and 79% for discrimination of metastases from gliomas and 88%, 85%, and 96% for discrimination of high-grade (grades III and IV) from low-grade (grade II) neoplasms. Multiclass classification was also performed via a one-vs-all voting scheme. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22131">
<title>Characterizing healthy and diseased white matter using quantitative magnetization transfer and multicomponent T2 relaxometry: A unified view via a four-pool model</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22131</link>
<description><![CDATA[Nuclear magnetic resonance relaxation and magnetization transfer in cerebral white matter can be described using a four-pool model: two for water protons (in separate myelin and intra/extracellular compartments) and two for protons associated with the lipids and proteins of biologic membranes (of myelin and nonmyelin semisolids). This model was used to gain insight into the observations from multicomponent quantitative T2 relaxometry and quantitative magnetization transfer imaging, both based on simplified white matter models and experimentally feasible in vivo. Using a set of coupled Bloch equations describing the behavior of the magnetization in a four-pool model of white matter, simulations of the quantitative T2 relaxometry and quantitative magnetization transfer imaging techniques were performed. Pathology-inspired modifications were made to the four-pool model to gauge their impact on quantitative T2 relaxometry and quantitative magnetization transfer imaging observations. Our results show that changes in the rate of water movement between microanatomic compartments may impact otherwise stable quantitative T2 relaxometry observations; that the measure of the quantitative magnetization transfer imaging-based semisolid pool population is robust, despite the presence of two distinct semisolid components; and that quantitative magnetization transfer imaging compartment size estimates are not influenced by changes in the T2 of the intra/extracellular water pool. The four-pool model, while impractical for in vivo characterization, yields important insight into the interpretation of changes observed with these quantitative MRI methods based on simplified models of white matter. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22109">
<title>Viable tumor tissue detection in murine metastatic breast cancer by whole-body MRI and multispectral analysis</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22109</link>
<description><![CDATA[Whole-body MRI combined with a semiautomated hierarchical multispectral image analysis technique was evaluated as a method for detecting viable tumor tissue in a murine model of metastatic breast cancer (4T1 cell line). Whole-body apparent diffusion coefficient, T2, and proton density maps were acquired in this study. The viable tumor tissue segmentation included three-stage k-means clustering of the parametric maps, morphologic operations, application of a size threshold, and reader discrimination of the segmented objects. The segmentation results were validated by histologic evaluation, and the detection accuracy of the technique was evaluated at three size thresholds (15, 100, and 500 voxels). The accuracy was 88.9% for a 500-voxel size threshold, and the area under receiver operating characteristic curve was 0.84. The regions of segmented viable tumor tissue within the primary tumors were found mostly on the periphery of the tumors in agreement with the histologic findings. The presented technique was found capable of detecting metastases and segmenting the viable tumor from necrotic regions within tumors found in this model. It offers a noninvasive, whole-body, viable tumor tissue detection method for preclinical and potentially clinical applications such as tumor screening and evaluating therapeutic efficacy. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22106">
<title>Complex-valued analysis of arterial spin labeling-based functional magnetic resonance imaging signals</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22106</link>
<description><![CDATA[Cerebral blood flow-dependent phase differences between tagged and control arterial spin labeling images are reported. A biophysical model is presented to explain the vascular origin of this difference. Arterial spin labeling data indicated that the phase difference is largest when the arterial component of the signals is preserved but is greatly reduced as the arterial contribution is suppressed by postinversion delays or flow-crushing gradients. Arterial vasculature imaging by saturation data of activation and hypercapnia conditions showed increases in phase accompanying blood flow increases.An arterial spin labeling functional magnetic resonance imaging study yielded significant activation by magnitude-only, phase-only, and complex analyses when preserving the whole arterial spin labeling signal. After suppression of the arterial signal by postinversion delays, magnitude-only and complex models yielded similar activation levels, but the phase-only model detected nearly no activation. When flow crushers were used for arterial suppression, magnitude-only activation was slightly lower and fluctuations in phase were dramatically higher than when postinversion delays were used.Although the complex analysis performed did not improve detection, a simulation study indicated that the complex-valued activation model exhibits combined magnitude and phase detection power and thus maximizes sensitivity under ideal conditions. This suggests that, as arterial spin labeling imaging and image correction methods develop, the complex-valued detection model may become helpful in signal detection. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22156">
<title>Characterization of T2* heterogeneity in human brain white matter</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22156</link>
<description><![CDATA[Recent in vivo MRI studies at 7.0 T have demonstrated extensive heterogeneity of T2* relaxation in white matter of the human brain. In order to study the origin of this heterogeneity, we performed T2* measurements at 1.5, 3.0, and 7.0 T in normal volunteers. Formalin-fixed brain tissue specimens were also studied using T2*-weighted MRI, histologic staining, chemical analysis, and electron microscopy. We found that T2* relaxation rate (R2* = 1/T2*) in white matter in living human brain is linearly dependent on the main magnetic field strength, and the T2* heterogeneity in white matter observed at 7.0 T can also be detected, albeit more weakly, at 1.5 and 3.0 T. The T2* heterogeneity exists also in white matter of the formalin-fixed brain tissue specimens, with prominent differences between the major fiber bundles such as the cingulum (CG) and the superior corona radiata. The white matter specimen with substantial difference in T2* has no significant difference in the total iron content, as determined by chemical analysis. On the other hand, evidence from histologic staining and electron microscopy demonstrates these tissue specimens have apparent difference in myelin content and microstructure. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22123">
<title>Superparamagnetic iron oxide nanoparticles as a dual imaging probe for targeting hepatocytes in vivo</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22123</link>
<description><![CDATA[Hepatocyte-specific targeting agents are useful for evaluation of the hepatocytic function and the monitoring of disease progress. Superparamagnetic iron oxide nanoparticles (SPION) bearing terminal galactose groups exhibit a high affinity for the asialoglycoprotein receptor on the hepatocyte surface. In this study, we synthesized and characterized the dual probe SPION detectable by both nuclear and MR imaging modality for specifically targeting hepatocytes in vivo. SPION with 12-nm diameter were functionalized with dopamine. Surface modification of the SPION was performed to target asialoglycoprotein receptor on hepatocytes, using lactobionic acid. Transmission electron microscope images demonstrated that SPION displayed highly uniform characteristics in terms of both particle size and shape. The X-ray diffraction pattern of SPION revealed a nanocrystal structure of magnetite. To radiolabel the magnetite with 99mTc, diethylenetriaminepentaacetic acid was conjugated to unreacted functional groups of dopamine. 99mTc-labeled lactobionic acid-SPION showed high accumulation in liver, with 38.43 ± 6.45% injected dose per gram. In MR imaging, the reduction of the T2 signal in the liver by lactobionic acid-SPION was approximately 50.8 ± 7.3%. Competition studies and transmission electron microscope images of liver tissues demonstrated that the lactobionic acid-SPION were localized in hepatocytes. Therefore, the lactobionic acid-SPION may be used as a hepatocyte-targeted dual contrast agent for both nuclear and MR imaging. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22113">
<title>Three-dimensional micro-MRI analysis of cerebral artery development in mouse embryos</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22113</link>
<description><![CDATA[Vascular system development involves a complex, three-dimensional branching process that is critical for normal embryogenesis. In the brain, the arterial systems appear to develop in a stereotyped fashion, but no detailed quantitative analyses of the mouse embryonic cerebral arteries have been described. In this study, a gadolinium-based contrast perfusion method was developed to selectively enhance the cerebral arteries in fixed mouse embryos. Three-dimensional magnetic resonance micro-imaging (micro-MRI) data were acquired simultaneously from multiple embryos staged between 10 and 17 days of gestation, and a variety of image analysis methods was used to extract and analyze the cerebral arterial patterns. The results show that the primary arterial branches in the mouse brain are very similar between individuals, with the patterns established early and growth occurring by extension of the segments, while maintaining the underlying vascular geometry. To investigate the utility of this method for mutant mouse phenotype analysis, contrast-enhanced micro-MRI data were acquired from Gli2-/- mutant embryos and their wild-type littermates, showing several previously unreported vascular phenotypes in Gli2-/- embryos, including the complete absence of the basilar artery. These results demonstrate that contrast-enhanced micro-MRI provides a powerful tool for analyzing vascular phenotypes in a variety of genetically engineered mice. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22101">
<title>Model-based blind estimation of kinetic parameters in dynamic contrast enhanced (DCE)-MRI</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22101</link>
<description><![CDATA[A method to simultaneously estimate the arterial input function (AIF) and pharmacokinetic model parameters from dynamic contrast-enhanced (DCE)-MRI data was developed. This algorithm uses a parameterized functional form to model the AIF and k-means clustering to classify tissue time-concentration measurements into a set of characteristic curves. An iterative blind estimation algorithm alternately estimated parameters for the input function and the pharmacokinetic model. Computer simulations were used to investigate the algorithm's sensitivity to noise and initial estimates. In 12 patients with sarcomas, pharmacokinetic parameter estimates were compared with "truth" obtained from model regression using a measured AIF. When arterial voxels were included in the blind estimation algorithm, the resulting AIF was similar to the measured input function. The "true" Ktrans values in tumor regions were not significantly different than the estimated values, 0.99 ± 0.41 and 0.86 ± 0.40 min-1, respectively, P = 0.27. "True" kep values also matched closely, 0.70 ± 0.24 and 0.65 ± 0.25 min-1, P = 0.08. When only tissue curves free of significant vascular contribution are used (vp < 0.05), the resulting AIF showed substantial delay and dispersion consistent with a more local AIF such as has been observed in dynamic susceptibility contrast imaging in the brain. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22091">
<title>High-frequency mode conversion technique for stiff lesion detection with magnetic resonance elastography (MRE)</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22091</link>
<description><![CDATA[A novel imaging technique is described in which the mode conversion of longitudinal waves is used for the qualitative detection of stiff lesions within soft tissue using magnetic resonance elastography (MRE) methods. Due to the viscoelastic nature of tissue, high-frequency shear waves attenuate rapidly in soft tissues but much less in stiff tissues. By introducing minimally-attenuating longitudinal waves at a significantly high frequency into tissue, shear waves produced at interfaces by mode conversion will be detectable in stiff regions, but will be significantly attenuated and thus not detectable in the surrounding soft tissue. This contrast can be used to detect the presence of stiff tissue. The proposed technique is shown to readily depict hard regions (mimicking tumors) present in tissue-simulating phantoms and ex vivo breast tissue. In vivo feasibility is demonstrated on a patient with liver metastases in whom the tumors are readily distinguished. Preliminary evidence also suggests that quantitative stiffness measurements of stiff regions obtained with this technique are more accurate than those from conventional MRE because of the short shear wavelengths. This rapid, qualitative technique may lend itself to applications in which the localization of stiff, suspicious neoplasms is coupled with more sensitive techniques for thorough characterization. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22132">
<title>High-contrast in vivo visualization of microvessels using novel FeCo/GC magnetic nanocrystals</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22132</link>
<description><![CDATA[FeCo-graphitic carbon shell nanocrystals are a novel MRI contrast agent with unprecedented high per-metal-atom-basis relaxivity (r1 = 97 mM-1 sec-1, r2 = 400 mM-1 sec-1) and multifunctional capabilities. While the conventional gadolinium-based contrast-enhanced angiographic magnetic MRI has proven useful for diagnosis of vascular diseases, its short circulation time and relatively low sensitivity render high-resolution MRI of morphologically small vascular structures such as those involved in collateral, arteriogenic, and angiogenic vessel formation challenging. Here, by combining FeCo-graphitic carbon shell nanocrystals with high-resolution MRI technique, we demonstrate that such microvessels down to [sim]100 [mu]m can be monitored in high contrast and noninvasively using a conventional 1.5-T clinical MRI system, achieving a diagnostic imaging standard approximating that of the more invasive X-ray angiography. Preliminary in vitro and in vivo toxicity study results also show no sign of toxicity. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22135">
<title>Magnetic susceptibility mapping of brain tissue in vivo using MRI phase data</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22135</link>
<description><![CDATA[Phase images in susceptibility-weighted MRI of brain provide excellent contrast. However, the phase is affected by tissue geometry and orientation relative to the main magnetic field (B0), and phase changes extend beyond areas of altered susceptibility. Magnetic susceptibility, on the other hand, is an intrinsic tissue property, closely reflecting tissue composition. Therefore, recently developed inverse Fourier-based methods were applied to calculate susceptibility maps from high-resolution phase images acquired at a single orientation at 7 T in the human brain (in vivo and fixed) and at 11.7 T in fixed marmoset brain. In susceptibility images, the contrast of cortical layers was more consistent than in phase images and was independent of the structures' orientation relative to B0. The contrast of iron-rich deep-brain structures (red nucleus and substantia nigra) in susceptibility images agreed more closely with iron-dominated R2* images than the phase image contrast, which extended outside the structures. The mean susceptibility in these regions was significantly correlated with their estimated iron content. Susceptibility maps calculated using this method overcome the orientation-dependence and non-locality of phase image contrast and seem to reflect underlying tissue composition. Susceptibility images should be easier to interpret than phase images and could improve our understanding of the sources of susceptibility contrast. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22174">
<title>Experimental and numerical assessment of MRI-induced temperature change and SAR distributions in phantoms and in vivo</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22174</link>
<description><![CDATA[It is important to accurately characterize the heating of tissues due to the radiofrequency energy applied during MRI. This has led to an increase in the use of numerical methods to predict specific energy absorption rate distributions for safety assurance in MRI. To ensure these methods are accurate for actual MRI coils, however, it is necessary to compare to experimental results. Here, we report results of some recent efforts to experimentally map temperature change and specific energy absorption rate in a phantom and in vivo where the only source of heat is the radiofrequency fields produced by the imaging coil. Results in a phantom match numerical simulation well, and preliminary results in vivo show measurable temperature increase. With further development, similar methods may be useful for verifying numerical methods for predicting specific energy absorption rate distributions and in some cases for directly measuring temperature changes and specific energy absorption rate induced by the radiofrequency fields in MRI experiments. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22163">
<title>Pattern recognition of MRSI data shows regions of glioma growth that agree with DTI markers of brain tumor infiltration</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22163</link>
<description><![CDATA[Gliomas are the most common primary brain tumors and the majority are highly malignant, with one of the worst prognoses for patients. Gliomas are characterized by invasive growth into normal brain tissue that makes complete surgical resection and accurate radiotherapy planning extremely difficult. We have performed independent component analysis of magnetic resonance spectroscopy imaging data from human gliomas to segment brain tissue into tumor core, tumor infiltration, and normal brain, with confirmation by diffusion tensor imaging analysis. Our data are consistent with previous studies that compared anomalies in isotropic and anisotropic diffusion images to determine regions of potential glioma infiltration. We show that coefficients of independent components can be used to create colored images for easy visual identification of regions of infiltrative tumor growth. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22161">
<title>Accelerating SENSE using compressed sensing</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22161</link>
<description><![CDATA[Both parallel MRI and compressed sensing (CS) are emerging techniques to accelerate conventional MRI by reducing the number of acquired data. The combination of parallel MRI and CS for further acceleration is of great interest. In this paper, we propose a novel method to combine sensitivity encoding (SENSE), one of the standard methods for parallel MRI, and compressed sensing for rapid MR imaging (SparseMRI), a recently proposed method for applying CS in MR imaging with Cartesian trajectories. The proposed method, named CS-SENSE, sequentially reconstructs a set of aliased reduced-field-of-view images in each channel using SparseMRI and then reconstructs the final image from the aliased images using Cartesian SENSE. The results from simulations and phantom and in vivo experiments demonstrate that CS-SENSE can achieve a reduction factor higher than those achieved by SparseMRI and SENSE individually and outperform the existing method that combines parallel MRI and CS. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22155">
<title>Assessment of the effects of cellular tissue properties on ADC measurements by numerical simulation of water diffusion</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22155</link>
<description><![CDATA[The apparent diffusion coefficient (ADC), as measured by diffusion-weighted MRI, has proven useful in the diagnosis and evaluation of ischemic stroke. The ADC of tissue water is reduced by 30-50% following ischemia and provides excellent contrast between normal and affected tissue. Despite its clinical utility, there is no consensus on the biophysical mechanism underlying the reduction in ADC. In this work, a numerical simulation of water diffusion is used to predict the effects of cellular tissue properties on experimentally measured ADC. The model indicates that the biophysical mechanisms responsible for changes in ADC postischemia depend upon the time over which diffusion is measured. At short diffusion times, the ADC is dependent upon the intrinsic intracellular diffusivity, while at longer, clinically relevant diffusion times, the ADC is highly dependent upon the cell volume fraction. The model also predicts that at clinically relevant diffusion times, the 30-50% drop in ADC after ischemia can be accounted for by cell swelling alone when intracellular T2 is allowed to be shorter than extracellular T2. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22151">
<title>Ex situ endorectal MRI probe for prostate imaging</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22151</link>
<description><![CDATA[A unique ex situ MRI probe, which examines samples external to its geometry, is presented. The probe is intended to be used for imaging the prostate gland via an endorectal pathway. It has a semicylindrical shape with a length of 6 cm and typical diameter of [sim]3 cm. The probe's imaging field of view spans almost along its entire length and up to a distance of 2 cm away from its surface, with an angular sector of [sim]90°. The detailed design of the probe is presented, followed by a set of representative results obtained by the current bench prototype of this system. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22150">
<title>Three-dimensional imaging of ventilation dynamics in asthmatics using multiecho projection acquisition with constrained reconstruction</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22150</link>
<description><![CDATA[The purpose of this work is to detect dynamic gas trapping in three dimensions during forced exhalation at isotropic high spatial resolution and high temporal resolution using hyperpolarized helium-3 MRI. Ten subjects underwent hyperpolarized helium-3 MRI and multidetector CT. MRI was performed throughout inspiration, breath-hold, and forced expiration. A multiecho three-dimensional projection acquisition was used to improve data collection efficiency and an iterative constrained reconstruction was implemented to improve signal to noise ratio (SNR) and increase robustness to motion. Two radiologists evaluated the dynamic MRI and breath-held multidetector CT data for gas and air trapping, respectively. Phantom studies showed the proposed technique significantly improved depiction of moving objects compared to view-sharing methods. Gas trapping was detected using MRI in five of the six asthmatic subjects who displayed air trapping with multidetector CT. Locations in disagreement were found to represent small to moderate regions of air trapping. The proposed technique provides whole-lung three-dimensional imaging of respiration dynamics at high spatial and temporal resolution and compares well to the current standard, multidetector CT. While multidetector CT can provide information about static regional air trapping, it is unable to depict dynamics in a setting more comparable to a spirometry maneuver and explore the longitudinal time evolution of the trapped regions. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22141">
<title>Detection of lactate with a hadamard slice selected, selective multiple quantum coherence, chemical shift imaging sequence (HDMD-SelMQC-CSI) on a clinical MRI scanner: Application to tumors and muscle ischemia</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22141</link>
<description><![CDATA[Lactate is an important metabolite in normal and malignant tissues detectable by NMR spectroscopy; however, it has been difficult to clinically detect the lactate methyl resonance because it is obscured by lipid resonances. The selective homonuclear multiple quantum coherence transfer technique offers a method for distinguishing lipid and lactate resonances. We implemented a three-dimensional selective homonuclear multiple quantum coherence transfer version with Hadamard slice selection and two-dimensional phase encoding (Hadamard encoded-selective homonuclear multiple quantum coherence transfer-chemical shift imaging) on a conventional clinical MR scanner. Hadamard slice selection is explained and demonstrated in vivo. This is followed by 1-cm3 resolution lactate imaging with detection to 5-mM concentration in 20 min on a 3-T clinical scanner. An analysis of QSel gradient duration and amplitude effects on lactate and lipid signal is presented. To demonstrate clinical feasibility, a 5-min lactate scan of a patient with a non-Hodgkin's lymphoma in the superficial thigh is reported. The elevated lactate signal coincides with the T2-weighted image of this tumor. As a test of selective homonuclear multiple quantum coherence transfer sensitivity, a thigh tourniquet was applied to a normal volunteer and an increase in lactate was detected immediately after tourniquet flow constriction. In conclusion, the Hadamard encoded-selective homonuclear multiple quantum coherence transfer-chemical shift imaging sequence is demonstrated on a phantom and in two lipid-rich, clinically relevant, in vivo conditions. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22140">
<title>Hybrid adiabatic-rectangular pulse train for effective saturation of magnetization within the whole heart at 3 T</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22140</link>
<description><![CDATA[Uniform T1-weighting is a major challenge for first-pass cardiac perfusion MRI at 3 T. Previously proposed adiabatic amplitude of radiofrequency field (B1)-insensitive rotation (BIR-4) pulse and standard and tailored pulse trains of three nonselective pulses have been important developments but each pulse has limitations at 3 T. As an extension of the tailored pulse train, we developed a hybrid pulse train by synergistically combining two nonselective rectangular radiofrequency pulses and an adiabatic half-passage pulse, in order to achieve effective saturation of magnetization within the heart, while remaining within clinically acceptable specific absorption rate limits. The standard pulse train, tailored pulse train, hybrid pulse train, and BIR-4 pulse train were evaluated through numerical, phantom, and in vivo experiments. Among the four saturation pulses, only the hybrid pulse train yielded residual magnetization <2% of equilibrium magnetization in the heart while remaining within clinically acceptable specific absorption rate limits for multislice first-pass cardiac perfusion MRI at 3 T. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22144">
<title>Magnetic resonance elastography: Inversions in bounded media</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22144</link>
<description><![CDATA[Magnetic resonance elastography is a noninvasive imaging technique capable of quantifying and spatially resolving the shear stiffness of soft tissues by visualization of synchronized mechanical wave displacement fields. However, magnetic resonance elastography inversions generally assume that the measured tissue motion consists primarily of shear waves propagating in a uniform, infinite medium. This assumption is not valid in organs such as the heart, eye, bladder, skin, fascia, bone and spinal cord, in which the shear wavelength approaches the geometric dimensions of the object. The aim of this study was to develop and test mathematical inversion algorithms capable of resolving shear stiffness from displacement maps of flexural waves propagating in bounded media such as beams, plates, and spherical shells, using geometry-specific equations of motion. Magnetic resonance elastography and finite element modeling of beam, plate, and spherical shell phantoms of various geometries were performed. Mechanical testing of the phantoms agreed with the stiffness values obtained from finite element modeling and magnetic resonance elastography data, and a linear correlation of r2 [ge] 0.99 was observed between the stiffness values obtained using magnetic resonance elastography and finite element modeling data. In conclusion, we have demonstrated new inversion methods for calculating shear stiffness that may be more appropriate for waves propagating in bounded media. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22153">
<title>High spatial and temporal resolution cardiac cine MRI from retrospective reconstruction of data acquired in real time using motion correction and resorting</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22153</link>
<description><![CDATA[Cine MRI is used for assessing cardiac function and flow and is typically based on a breath-held, segmented data acquisition. Breath holding is particularly difficult for patients with congestive heart failure or in pediatric cases. Real-time imaging may be used without breath holding or ECG triggering. However, despite the use of rapid imaging sequences and accelerated parallel imaging, real-time imaging typically has compromised spatial and temporal resolution compared with gated, segmented breath-held studies. A new method is proposed that produces a cardiac cine across the full cycle, with both high spatial and temporal resolution from a retrospective reconstruction of data acquired over multiple heartbeats during free breathing. The proposed method was compared with conventional cine images in 10 subjects. The resultant image quality for the proposed method (4.2 ± 0.4) without breath holding or gating was comparable to the conventional cine (4.4 ± 0.5) on a five-point scale (P = n.s.). Motion-corrected averaging of real-time acquired cardiac images provides a means of attaining high-quality cine images with many of the benefits of real-time imaging, such as free-breathing acquisition and tolerance to arrhythmias. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22146">
<title>In vivo proton MRS to quantify anesthetic effects of pentobarbital on cerebral metabolism and brain activity in rat</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22146</link>
<description><![CDATA[To quantitatively investigate the effects of pentobarbital anesthesia on brain activity, brain metabolite concentrations and cerebral metabolic rate of glucose, in vivo proton MR spectra, and electroencephalography were measured in the rat brain with various doses of pentobarbital. The results show that (1) the resonances attributed to propylene glycol, a solvent in pentobarbital injection solution, can be robustly detected and quantified in the brain; (2) the concentration of most brain metabolites remained constant under the isoelectric state (silent electroencephalography) with a high dose of pentobarbital compared to mild isoflurane anesthesia condition, except for a reduction of 61% in the brain glucose level, which was associated with a 37% decrease in cerebral metabolic rate of glucose, suggesting a significant amount of "housekeeping" energy for maintaining brain cellular integrity under the isoelectric state; and (3) electroencephalography and cerebral metabolic activities were tightly coupled to the pentobarbital anesthesia depth and they can be indirectly quantified by the propylene glycol resonance signal at 1.13 ppm. This study indicates that in vivo proton MR spectroscopy can be used to measure changes in cerebral metabolite concentrations and cerebral metabolic rate of glucose under varied pentobarbital anesthesia states; moreover, the propylene glycol signal provides a sensitive biomarker for quantitatively monitoring these changes and anesthesia depth noninvasively. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22160">
<title>Simplified 13C metabolic modeling for simplified measurements of cerebral TCA cycle rate in vivo</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22160</link>
<description><![CDATA[13C NMR spectroscopy is a unique tool to measure the cerebral tricarboxylic acid (TCA) cycle rate in vivo. The measurement relies on metabolic modeling of glutamate C3 and C4 enrichment time courses during a 13C-glucose intravenous infusion. Usual metabolic models require the plasma glucose and 13C-glucose time courses as input functions, as well as the knowledge of Michaelis-Menten kinetics parameters governing passage through the blood-brain barrier. It is shown in the present work that, when using an infusion protocol yielding a rapidly stable plasma glucose fractional enrichment, metabolic modeling can be simplified in such a manner that this additional information on input function and glucose transport is no longer required, significantly simplifying the measurement of cerebral TCA cycle rate in vivo. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://dx.doi.org/10.1002%2Fmrm.22119">
<title>Quantification of non-water-suppressed MR spectra with correction for motion-induced signal reduction</title>
<link>http://dx.doi.org/10.1002%2Fmrm.22119</link>
<description><![CDATA[Intrascan subject movement in clinical MR spectroscopic examinations may result in inconsistent water suppression that distorts the metabolite signals, frame-to-frame variations in spectral phase and frequency, and consequent reductions in the signal-to-noise ratio due to destructive averaging. Frame-to-frame phase/frequency corrections, although reported to be successful in achieving constructive averaging, rely on consistent water suppression, which may be difficult in the presence of intrascan motion. In this study, motion correction using non-water-suppressed data acquisition is proposed to overcome the above difficulties. The time-domain matrix-pencil postprocessing method was used to extract water signals from the non-water-suppressed spectroscopic data, followed by phase and frequency corrections of the metabolite signals based on information obtained from the water signals. From in vivo experiments on seven healthy subjects at 3.0 T, quantification of metabolites using the unsuppressed water signal as a reference showed improved correlation with water-suppressed data acquired in the absence of motion (R2 = 0.9669; slope = 0.94). The metabolite concentrations derived using the proposed approach were in good agreement with literature values. Computer simulations under various degrees of frequency and phase variations further demonstrated robust performance of the time-domain postprocessing approach. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.]]></description>
</item>

<item rdf:about="http://www.springerlink.com/content/m0v1521787g2q373/">
<title>Structural&#x2013;acoustic modal analysis of cylindrical shells: application to MRI scanner systems</title>
<link>http://www.springerlink.com/content/m0v1521787g2q373/</link>
<description><![CDATA[Abstract
 Object&nbsp;&nbsp;The acoustic noise in a magnetic resonance imaging (MRI) scanner bore is mainly introduced by the vibration of gradient coils.
 The interaction between acoustic modes in the scanner bore and structure modes in the coil structure leads to structural–acoustic
 coupling. In order to implement quiet MRI design, the structural–acoustic coupling mechanism in MRI machines needs to be fully
 investigated.
 
 
 
 Materials and method&nbsp;&nbsp;Structural analysis was first implemented using Love’s classical shell theory. The concept of a “virtually closed cavity”
 was used in the acoustic modal analysis of the gradient coil duct. The dispersion curves and the number of modes per frequency
 band were used to reveal modal distribution properties for both structural modes and acoustic modes. Structural–acoustic coupling
 modes were identified by superposition of the dispersion diagrams of the structural waves and acoustic waves. Experimental
 validation was implemented separately for the structural analysis and acoustic analysis.
 
 
 
 Results&nbsp;&nbsp;Independent structural modes and acoustic modes and their distribution patterns were calculated up to 3000Hz with various
 boundary conditions. Coupling modes were clearly revealed using the analysis procedures presented in this paper and were found
 to be in agreement with the ones identified from experimental measurements.
 
 
 
 Conclusion&nbsp;&nbsp;These methods are effective for coupled and uncoupled modal analysis of MRI scanner systems and can be used for quiet MRI
 design or sound absorber design for existing MRI systems.
 
 
 
	Content Type Journal ArticleCategory Research ArticleDOI 10.1007/s10334-009-0185-zAuthors
		Gemin Li, Queen’s University Department of Mechanical Engineering McLaughlin Hall Kingston ON K7L 3N6 CanadaChris K. Mechefske, Queen’s University Department of Mechanical Engineering McLaughlin Hall Kingston ON K7L 3N6 Canada
	

	
		Journal Magnetic Resonance Materials in Physics, Biology and MedicineOnline ISSN 1352-8661Print ISSN 0968-5243
	
]]></description>
</item>

<item rdf:about="http://www.springerlink.com/content/h3714r0191m73487/">
<title>Quantitative metabolic profiles of 2nd and 3rd trimester human amniotic fluid using 1H HR-MAS spectroscopy</title>
<link>http://www.springerlink.com/content/h3714r0191m73487/</link>
<description><![CDATA[Abstract
 Object&nbsp;&nbsp;To establish and compare normative metabolite concentrations in 2nd and 3rd trimester human amniotic fluid samples in an effort
 to reveal metabolic biomarkers of fetal health and development.
 
 
 
 Materials and methods&nbsp;&nbsp;Twenty-one metabolite concentrations were compared between 2nd (15–27 weeks gestation, N = 23) and 3rd (29–39 weeks gestation, N = 27) trimester amniotic fluid samples using 1H high resolution magic angle spinning (HR-MAS) spectroscopy. Data were acquired using the electronic reference to access
 in vivo concentrations method and quantified using a modified semi-parametric quantum estimation algorithm modified for high-resolution
 ex vivo data.
 
 
 
 Results&nbsp;&nbsp;Sixteen of 21 metabolite concentrations differed significantly between 2nd and 3rd trimester groups. Betaine (0.00846±0.00206
 mmol/kg vs. 0.0133±0.0058&nbsp;mmol/kg, P &lt; 0.002) and creatinine (0.0124±0.0058&nbsp;mmol/kg vs. 0.247±0.011&nbsp;mmol/kg, P &lt; 0.001) concentrations increased significantly, while glucose (5.96±1.66&nbsp;mmol/kg vs. 2.41±1.69 mmol/kg, P &lt; 0.001), citrate (0.740±0.217 mmol/kg vs. 0.399±0.137&nbsp;mmol/kg, P &lt; 0.001), pyruvate (0.0659±0.0103&nbsp;mmol/kg vs. 0.0299±0.286&nbsp;mmol/kg, P &lt; 0.001), and numerous amino acid (e.g. alanine, glutamate, isoleucine, leucine, lysine, and valine) concentrations decreased
 significantly with advancing gestation. A stepwise multiple linear regression model applied to 50 samples showed that gestational
 age can be accurately predicted using combinations of alanine, glucose and creatinine concentrations.
 
 
 
 Conclusion&nbsp;&nbsp;These results provide key normative data for 2nd and 3rd trimester amniotic fluid metabolite concentrations and provide the
 foundation for future development of magnetic resonance spectroscopy (MRS) biomarkers to evaluate fetal health and development.
 
 
 
	Content Type Journal ArticleCategory Research ArticleDOI 10.1007/s10334-009-0184-0Authors
		Brad R. Cohn, University of California Department of Radiology & Biomedical Imaging 1600 Divisadero Street, Room C-250 Box 1667 San Francisco CA 94115 USABonnie N. Joe, University of California Department of Radiology & Biomedical Imaging 1600 Divisadero Street, Room C-250 Box 1667 San Francisco CA 94115 USAShoujun Zhao, University of California Department of Radiology & Biomedical Imaging 1600 Divisadero Street, Room C-250 Box 1667 San Francisco CA 94115 USAJohn Kornak, University of California Department of Radiology & Biomedical Imaging 1600 Divisadero Street, Room C-250 Box 1667 San Francisco CA 94115 USAVickie Y. Zhang, University of California Department of Radiology & Biomedical Imaging 1600 Divisadero Street, Room C-250 Box 1667 San Francisco CA 94115 USARahwa Iman, University of California Department of Radiology & Biomedical Imaging 1600 Divisadero Street, Room C-250 Box 1667 San Francisco CA 94115 USAJohn Kurhanewicz, University of California Department of Radiology & Biomedical Imaging 1600 Divisadero Street, Room C-250 Box 1667 San Francisco CA 94115 USAKiarash Vahidi, University of California Department of Radiology & Biomedical Imaging 1600 Divisadero Street, Room C-250 Box 1667 San Francisco CA 94115 USAJingwei Yu, University of California Department of Laboratory Medicine San Francisco CA USAAaron B. Caughey, University of California Department of Obstetrics & Gynecology San Francisco CA USAMark G. Swanson, University of California Department of Radiology & Biomedical Imaging 1600 Divisadero Street, Room C-250 Box 1667 San Francisco CA 94115 USA
	

	
		Journal Magnetic Resonance Materials in Physics, Biology and MedicineOnline ISSN 1352-8661Print ISSN 0968-5243
	
]]></description>
</item>

<item rdf:about="http://www.springerlink.com/content/x465x44qp5g602hu/">
<title>ESMRMB 2009 Congress, Antalya, Turkey, 1&#x2013;3 October: Abstracts, Thursday</title>
<link>http://www.springerlink.com/content/x465x44qp5g602hu/</link>
<description><![CDATA[ESMRMB 2009 Congress, Antalya, Turkey, 1–3 October: Abstracts, Thursday
	Content Type Journal ArticleDOI 10.1007/s10334-009-0175-1

	
		Journal Magnetic Resonance Materials in Physics, Biology and MedicineOnline ISSN 1352-8661Print ISSN 0968-5243
	
		Journal Volume Volume 22
	
		Journal Issue Volume 22, Supplement 1 / October, 2009
	
]]></description>
</item>

<item rdf:about="http://www.springerlink.com/content/n321070n31w521u1/">
<title>ESMRMB 2009 Congress, Antalya, Turkey, 1&#x2013;3 October: Abstracts, Saturday</title>
<link>http://www.springerlink.com/content/n321070n31w521u1/</link>
<description><![CDATA[ESMRMB 2009 Congress, Antalya, Turkey, 1–3 October: Abstracts, Saturday
	Content Type Journal ArticleDOI 10.1007/s10334-009-0177-z

	
		Journal Magnetic Resonance Materials in Physics, Biology and MedicineOnline ISSN 1352-8661Print ISSN 0968-5243
	
		Journal Volume Volume 22
	
		Journal Issue Volume 22, Supplement 1 / October, 2009
	
]]></description>
</item>

<item rdf:about="http://www.springerlink.com/content/eg84ux863t66x5w7/">
<title>ESMRMB 2009 Congress, Antalya, Turkey, 1&#x2013;3 October: Abstracts, Friday</title>
<link>http://www.springerlink.com/content/eg84ux863t66x5w7/</link>
<description><![CDATA[ESMRMB 2009 Congress, Antalya, Turkey, 1–3 October: Abstracts, Friday
	Content Type Journal ArticleDOI 10.1007/s10334-009-0176-0

	
		Journal Magnetic Resonance Materials in Physics, Biology and MedicineOnline ISSN 1352-8661Print ISSN 0968-5243
	
		Journal Volume Volume 22
	
		Journal Issue Volume 22, Supplement 1 / October, 2009
	
]]></description>
</item>

<item rdf:about="http://www.springerlink.com/content/w37qrw112gjhn200/">
<title>ESMRMB 2009 Congress, Antalya, Turkey, 1&#x2013;3 October: EPOStm Posters / Paper Posters / Info-RESO</title>
<link>http://www.springerlink.com/content/w37qrw112gjhn200/</link>
<description><![CDATA[ESMRMB 2009 Congress, Antalya, Turkey, 1–3 October: EPOStm Posters / Paper Posters / Info-RESO
	Content Type Journal ArticleDOI 10.1007/s10334-009-0178-y

	
		Journal Magnetic Resonance Materials in Physics, Biology and MedicineOnline ISSN 1352-8661Print ISSN 0968-5243
	
		Journal Volume Volume 22
	
		Journal Issue Volume 22, Supplement 1 / October, 2009
	
]]></description>
</item>

<item rdf:about="http://www.springerlink.com/content/m8n573514vj23503/">
<title>ESMRMB 2009 Congress, Antalya, Turkey, 1&#x2013;3 October: Author Index</title>
<link>http://www.springerlink.com/content/m8n573514vj23503/</link>
<description><![CDATA[ESMRMB 2009 Congress, Antalya, Turkey, 1–3 October: Author Index
	Content Type Journal ArticleDOI 10.1007/s10334-009-0179-x

	
		Journal Magnetic Resonance Materials in Physics, Biology and MedicineOnline ISSN 1352-8661Print ISSN 0968-5243
	
		Journal Volume Volume 22
	
		Journal Issue Volume 22, Supplement 1 / October, 2009
	
]]></description>
</item>

<item rdf:about="http://www.springerlink.com/content/m272hu6038q15368/">
<title>A digital receiver with fast frequency- and gain-switching capabilities for MRI systems</title>
<link>http://www.springerlink.com/content/m272hu6038q15368/</link>
<description><![CDATA[Abstract
 Object&nbsp;&nbsp;In this article, two issues pertaining to MRI digital receivers are addressed. One is the maintenance of phase coherence between
 the transmitter and the receiver—an effective solution is proposed, in which the receiver frequency is switched synchronously
 with the transmitter frequency. The other is the dynamic range of the receiver—gain-switching technique is utilized to improve
 the dynamic range. To meet the hardware requirements of these solutions, a digital receiver with fast frequency- and gain-switching
 capabilities was implemented.
 
 
 
 Materials and methods&nbsp;&nbsp;The primary components of the proposed digital receiver are a variable gain amplifier, a high-speed analog-to-digital converter
 and a single-chip digital receiver core. The radio-frequency magnetic resonance signal is directly sampled by the analog-to-digital
 converter and processed in the digital receiver core. By pre-storing the receiver waveform in the on-board SDRAM, the frequency
 and gain of the receiver may be switched very quickly.
 
 
 
 Results&nbsp;&nbsp;The performance of the proposed digital receiver is verified by embedding it in an imaging spectrometer. It is then demonstrated
 by conducting experiments on a home-built 0.3-T magnetic resonance imaging system.
 
 
 
 Conclusion&nbsp;&nbsp;The results show that the phase coherence between the transmitter and the receiver and the dynamic range of the receiver are
 greatly improved. Consequently, the proposed digital receiver may be useful for obtaining multiple-slice two-dimensional magnetic
 resonance images with very high resolution.
 
 
 
	Content Type Journal ArticleCategory Research ArticleDOI 10.1007/s10334-009-0182-2Authors
		Ning Ruipeng, East China Normal University Shanghai Key Laboratory of Functional Magnetic Resonance Imaging, Department of Physics 3663 North Zhong-Shan Road 200062 Shanghai People’s Republic of ChinaDai Yidong, East China Normal University Shanghai Key Laboratory of Functional Magnetic Resonance Imaging, Department of Physics 3663 North Zhong-Shan Road 200062 Shanghai People’s Republic of ChinaYang Guang, East China Normal University Shanghai Key Laboratory of Functional Magnetic Resonance Imaging, Department of Physics 3663 North Zhong-Shan Road 200062 Shanghai People’s Republic of ChinaLi Gengying, East China Normal University Shanghai Key Laboratory of Functional Magnetic Resonance Imaging, Department of Physics 3663 North Zhong-Shan Road 200062 Shanghai People’s Republic of China
	

	
		Journal Magnetic Resonance Materials in Physics, Biology and MedicineOnline ISSN 1352-8661Print ISSN 0968-5243
	
]]></description>
</item>

<item rdf:about="http://www.springerlink.com/content/k03542jux12472x8/">
<title>Influence of cardiac motion on diffusion-weighted magnetic resonance imaging of the liver</title>
<link>http://www.springerlink.com/content/k03542jux12472x8/</link>
<description><![CDATA[Abstract
 Purpose&nbsp;&nbsp;To assess cardiac motion-induced signal loss in diffusion-weighted magnetic resonance imaging (DWI) of the liver using dynamic
 DWI.
 
 
 
 Materials and methods&nbsp;&nbsp;Three volunteers underwent dynamic coronal DWI of the liver under breathholding, in the diastolic (DWIdiast) or systolic (DWIsyst) cardiac phase, and with motion probing gradients (MPGs) in phase encoding (P, left–right), frequency encoding (M, superior–inferior),
 or slice select (S, anterior–posterior) direction. Liver-to-background contrasts (LBCs) of DWIsyst were compared to those of DWIdiast, for both the left and right liver lobes, using nonparametric tests. Signal decrease ratios (SDRs) were calculated as (1−(LBCDWIsyst/LBCDWIdiast)) ×&nbsp;100%. DWIsyst was further analyzed to determine which direction of MPGs was most affected by cardiac motion.
 
 
 
 Results&nbsp;&nbsp;In the left liver lobe, LBCs of DWIsyst (median 3.35) were significantly lower (P &lt;&nbsp;0.0001) than those of DWIdiast (median 4.84). In the right liver lobe, LBCs of DWIsyst (median 4.17) were also significantly lower (P &lt;&nbsp;0.0001) than those of DWIdiast (median 5.35 ). SDRs of the left and right liver lobes were 25.5% and 17.3%, respectively. In DWIsyst, the significantly lowest (P &lt;&nbsp;0.05) LBCs were observed in the M direction (left liver lobe) and P direction (right liver lobe) of MPGs.
 
 
 
 Conclusion&nbsp;&nbsp;Signal intensity of both liver lobes are affected by cardiac motion in DWI. In the left liver lobe, signal loss especially
 occurs in the superior–inferior direction of MPGs, whereas in the right lobe, signal loss especially occurs in the left-right
 direction of MPGs.
 
 
 
	Content Type Journal ArticleCategory Research ArticleDOI 10.1007/s10334-009-0183-1Authors
		Thomas C. Kwee, University Medical Center Utrecht Department of Radiology Heidelberglaan 100 3584 CX Utrecht The NetherlandsTaro Takahara, University Medical Center Utrecht Department of Radiology Heidelberglaan 100 3584 CX Utrecht The NetherlandsTetsu Niwa, University Medical Center Utrecht Department of Radiology Heidelberglaan 100 3584 CX Utrecht The NetherlandsMarko K. Ivancevic, University of Michigan Medical Center Department of Radiology Ann Arbor MI USAGwenael Herigault, Philips Healthcare Best The NetherlandsMarc Van Cauteren, Philips Healthcare Asia Pacific Tokyo JapanPeter R. Luijten, University Medical Center Utrecht Department of Radiology Heidelberglaan 100 3584 CX Utrecht The Netherlands
	

	
		Journal Magnetic Resonance Materials in Physics, Biology and MedicineOnline ISSN 1352-8661Print ISSN 0968-5243
	
		Journal Volume Volume 22
	
		Journal Issue Volume 22, Number 5 / October, 2009
	
]]></description>
</item>

<item rdf:about="http://www.springerlink.com/content/80jk2k36185208x7/">
<title>Rapid 3-D mapping of hyperpolarized 3He spin-lattice relaxation times using variable flip angle gradient echo imaging with application to alveolar oxygen partial pressure measurement in rat lungs</title>
<link>http://www.springerlink.com/content/80jk2k36185208x7/</link>
<description><![CDATA[Abstract
 Objective&nbsp;&nbsp;The purpose of this work was to develop a rapid 3-D, variable flip angle (VFA) method for measurement of hyperpolarized 3He T
 1 which accounts for the effects of radiofrequency (RF) pulses without the need for additional flip angle information.
 
 
 
 Materials and methods&nbsp;&nbsp;The 3-D, VFA method was validated in vitro over a range of oxygen partial pressures ranging from 0.04 to 0.52&nbsp;atm. The approach
 was also tested in vivo in five healthy rats as a function of increasing number of wash-out breaths. The T
 1 accuracy of the VFA method in the presence of flip angle mis-setting and RF field non-uniformity was compared with the CFA
 method using simulations and experiments.
 
 
 
 Results&nbsp;&nbsp;
 T
 1 measurements were found to provide pAO2 estimates, both in vitro and in vivo consistent with those predicted based on gas dilution and/or ventilation para- meters.
 For the RF pulse mis-setting (4%) and RF field non-uniformity (3%) used here, the VFA method provided a T
 1 accuracy of better than 5% compared to 12% for the CFA method.
 
 
 
 Conclusion&nbsp;&nbsp;With sufficient RF field homogeneity (3%) and proper calibration (4%), the VFA approach can provide rapid and reliable 3-D
 T
 1 mapping of hyperpolarized 3He without the need for additional flip angle information.
 
 
 
	Content Type Journal ArticleCategory Research ArticleDOI 10.1007/s10334-009-0181-3Authors
		Alexei V. Ouriadov, Robarts Research Institute Imaging Research Laboratories P.O. Box 5015 100 Perth Drive London ON N6A 5K8 CanadaWilfred W. Lam, Sunnybrook Health Sciences Centre Imaging Research Toronto ON M4N 3M5 CanadaGiles E. Santyr, Robarts Research Institute Imaging Research Laboratories P.O. Box 5015 100 Perth Drive London ON N6A 5K8 Canada
	

	
		Journal Magnetic Resonance Materials in Physics, Biology and MedicineOnline ISSN 1352-8661Print ISSN 0968-5243
	
		Journal Volume Volume 22
	
		Journal Issue Volume 22, Number 5 / October, 2009
	
]]></description>
</item>

<item rdf:about="http://www.springerlink.com/content/302j862118204454/">
<title>Utilizing different methods for visualizing susceptibility from a single multi-gradient echo dataset</title>
<link>http://www.springerlink.com/content/302j862118204454/</link>
<description><![CDATA[Abstract
 Purpose&nbsp;&nbsp;Objects that cause a susceptibility gradient can generate regions of hypo-intensity in MRI. MR techniques developed for positive
 enhancement of such objects require sequence parameter optimization. Thus comparison of images acquired successively using
 different techniques is difficult since different parameter settings result in variations in signal and noise. A new method
 is presented that allows production of positive contrast images, a relaxation rate 

R2*
-map and negative contrast images from a single dataset by post-processing.
 
 
 
 Methods&nbsp;&nbsp;Positive contrast techniques considered include the “white marker” technique, inversion-recovery on-resonance (IRON) and susceptibility
 gradient mapping (SGM). The new method was tested in phantoms of iron-oxide agent gel solutions and prostate marker seeds.
 Images produced by post-processing were compared with those obtained directly. The post-processing technique was applied in
 vivo for the visualization of iron-oxide contrast agent uptake in a balloon-injured swine carotid model.
 
 
 
 Results&nbsp;&nbsp;The images produced in the post-processing step allowed determination of optimal parameter settings for each technique. SGM
 was found to provide the greatest positive contrast, whilst the 

T2*
-weighted images provide more sensitivity to regions that exhibited weaker susceptibility effects.
 
 
 
 Conclusions&nbsp;&nbsp;Combined 

T2*
-weighted imaging and SGM using the same complex image data was found to provide complementary information and high sensitivity
 to detect distortion inducing agents.
 
 
 
	Content Type Journal ArticleCategory Research ArticleDOI 10.1007/s10334-009-0180-4Authors
		Gopal Varma, King’s College London, St Thomas’ Hospital Division of Imaging Sciences Westminster Bridge Road London SE1 7EH UKSteen Fjord Pedersen, University of Aarhus, Aarhus University Hospital The MR Research Centre Skejby, Brendstrupgaardsvej 8200 Aarhus N DenmarkMatthias Taupitz, Charite-Universitatsmedizin Berlin Department of Radiology Campus Charite Mitte, Chariteplatz 1 10117 Berlin GermanyRene Michael Botnar, King’s College London, St Thomas’ Hospital Division of Imaging Sciences Westminster Bridge Road London SE1 7EH UKHannes Dahnke, Philips Research Europe Roentgenstrasse 24-26 22335 Hamburg GermanyStephen Frederick Keevil, King’s College London, St Thomas’ Hospital Division of Imaging Sciences Westminster Bridge Road London SE1 7EH UKTobias Schaeffter, King’s College London, St Thomas’ Hospital Division of Imaging Sciences Westminster Bridge Road London SE1 7EH UK
	

	
		Journal Magnetic Resonance Materials in Physics, Biology and MedicineOnline ISSN 1352-8661Print ISSN 0968-5243
	
		Journal Volume Volume 22
	
		Journal Issue Volume 22, Number 5 / October, 2009
	
]]></description>
</item>

<item rdf:about="http://www.springerlink.com/content/l4335707v00l8571/">
<title>Influence of selecting EPI readout-encoding bandwidths on arterial spin labeling perfusion MRI</title>
<link>http://www.springerlink.com/content/l4335707v00l8571/</link>
<description><![CDATA[Abstract
 Object&nbsp;&nbsp;The objective of this study was to investigate effects of varying readout bandwidths on the arterial spin labeling (ASL)-perfusion
 MRI measurements at a high magnetic field MRI system.
 
 
 
 Materials and methods&nbsp;&nbsp;Brain perfusion studies were performed on nine volunteers (four males, five females) using flow sensitive alternating inversion
 recovery (FAIR) ASL single-shot echo-planar imaging (EPI)-MRI. To investigate EPI bandwidth effects on the time-series perfusion-weighted
 imaging (PWI) data, two regions-of-interest (ROI) were placed outside the brain to determine the level of noise and another
 ROI inside the brain to determine the level of signal. Coefficients of variations (CoV) were calculated for the time-series
 PWI data. One-way analysis of variance (ANOVA) was used to investigate voxel-wise differences in the time-series PWI data
 between two different bandwidth values.
 
 
 
 Results&nbsp;&nbsp;At the level of ROI, there was no significant effect of changing EPI bandwidths on the time-series PWI data in any of the
 volunteers (P&nbsp;&gt;&nbsp;0.031). In contrast, CoV values over the dynamic PWI data varied with depending on selecting EPI bandwidths and voxel-based
 tests showed that N2 ghosting, modulated by EPI bandwidth, can appear in some brain regions, especially in areas that overlap
 with the spatial distribution of N2 ghosting artifacts.
 
 
 
 Conclusions&nbsp;&nbsp;Although N2 ghosting can be reduced by adjusting the bandwidth of EPI on the time-series of PWI data, the effects cannot be
 entirely eliminated. In particular, N2 ghosting can bias CBF quantification if EPI control scans to determine the equilibrium-state
 signal are confounded by N2 ghosting. Therefore, careful tuning of the bandwidth of EPI is necessary to avoid artifacts in
 the ASL signal from N2-ghosting.
 
 
 
	Content Type Journal ArticleCategory Research ArticleDOI 10.1007/s10334-009-0174-2Authors
		Geon-Ho Jahng, Kyung Hee University Department of Radiology, School of Medicine, East-West Neo Medical Center 149 Sangil-dong, Gangdong-gu Seoul 134-090 South KoreaNorbert Schuff, University of California, San Francisco Department of Radiology, Center for Imaging of Neurodegenerative Diseases, VA Medical Center 4150 Clement Street, 114M San Francisco CA 94121 USA
	

	
		Journal Magnetic Resonance Materials in Physics, Biology and MedicineOnline ISSN 1352-8661Print ISSN 0968-5243
	
		Journal Volume Volume 22
	
		Journal Issue Volume 22, Number 5 / October, 2009
	
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</item>

<item rdf:about="http://www.springerlink.com/content/702w1vv7r233n027/">
<title>Echo-dephased steady state free precession</title>
<link>http://www.springerlink.com/content/702w1vv7r233n027/</link>
<description><![CDATA[Abstract
 Objective&nbsp;&nbsp;To introduce a novel positive contrast method for passive localization and visualization of paramagnetic susceptibility markers.
 
 
 
 Materials and methods&nbsp;&nbsp;The novel approach is based on an echo-dephased steady-state free precession (SSFP) sequence. Gradients dephase any signal
 by ±π at the centered echo-time (TE =&nbsp;TR/2) and induce a total dephasing of ±2π per pixel within TR. This ensures that background
 tissues do not contribute to signal formation and thus appear dark. However, within the close vicinity of the paramagnetic
 marker, local gradient fields compensate for the intrinsic dephasing to form an echo. Conceptual issues of gradient compensation
 and its visualization characteristics are analyzed. The feasibility of the proposed technique for MR-guided intravascular
 interventions is demonstrated using flow phantom.
 
 
 
 Results&nbsp;&nbsp;Echo-dephased SSFP is able to localize and visualize paramagnetic marker with excellent suppression of the background signals.
 The flow phantom experiments concluded that reliable tracking of the interventional guidewire is feasible using echo-dephased
 SSFP.
 
 
 
 Conclusion&nbsp;&nbsp;With newly introduced echo-dephased SSFP approach, accurate and reliable visualization of paramagnetic interventional device
 is feasible.
 
 
 
	Content Type Journal ArticleCategory Research ArticleDOI 10.1007/s10334-009-0173-3Authors
		Sunil Patil, University of Basel Hospital Division of Radiological Physics, Department of Medical Radiology Petersgraben 4 4031 Basel SwitzerlandOliver Bieri, University of Basel Hospital Division of Radiological Physics, Department of Medical Radiology Petersgraben 4 4031 Basel SwitzerlandKlaus Scheffler, University of Basel Hospital Division of Radiological Physics, Department of Medical Radiology Petersgraben 4 4031 Basel Switzerland
	

	
		Journal Magnetic Resonance Materials in Physics, Biology and MedicineOnline ISSN 1352-8661Print ISSN 0968-5243
	
		Journal Volume Volume 22
	
		Journal Issue Volume 22, Number 5 / October, 2009
	
]]></description>
</item>

<item rdf:about="http://www.springerlink.com/content/h4656r3022058743/">
<title>Monitoring the survival of islet transplants by MRI using a novel technique for their automated detection and quantification</title>
<link>http://www.springerlink.com/content/h4656r3022058743/</link>
<description><![CDATA[Abstract
 Object&nbsp;&nbsp;There is a clinical need to be able to assess graft loss of transplanted pancreatic islets (PI) non-invasively with clear-cut
 quantification of islet survival. We tracked transplanted PI in diabetic mice during the early post-transplant period by magnetic
 resonance imaging (MRI) and quantified the islet loss using automatic segmentation technique.
 
 
 
 Materials and methods&nbsp;&nbsp;Magnetically labeled islet iso-, allo- and xenografts were injected into the right liver lobes. Animals underwent MRI scanning
 during 14 days after PI transplantation. MR images were processed using custom-made software, which automatically detects
 hypointense regions representing PI. It is based on morphological top-hat and bottom-hat transforms.
 
 
 
 Results&nbsp;&nbsp;Manually and automatically detected areas, corresponding to PI, differed by 4% in phantoms. Signal loss regions due to PI
 decreased comparably in all groups during the first week post transplant. Throughout the second week post-transplant, the
 signal loss area continued in a steep decline in case of allografts and xenografts, whereas the decline in case of isografts
 slowed down.
 
 
 
 Conclusion&nbsp;&nbsp;Automatic segmentation allows for the more reproducible, objective assessment of transplanted PI. Quantification confirms
 the assumption that a significant number of islets are destroyed in the first week following transplantation irrespective
 of allografts, xenografts or isografts.
 
 
 
	Content Type Journal ArticleCategory Research ArticleDOI 10.1007/s10334-009-0172-4Authors
		Daniel Jirak, Robarts Research Institute Imaging Research Laboratories London ON N6A 5K8 CanadaJan Kriz, Robarts Research Institute Imaging Research Laboratories London ON N6A 5K8 CanadaMichal Strzelecki, Technical University of Lodz Institute of Electronics Lodz PolandJiabi Yang, Robarts Research Institute Transplantation Group London ON CanadaCraig Hasilo, Robarts Research Institute Transplantation Group London ON CanadaDavid J. White, Robarts Research Institute Transplantation Group London ON CanadaPaula J. Foster, Robarts Research Institute Imaging Research Laboratories London ON N6A 5K8 Canada
	

	
		Journal Magnetic Resonance Materials in Physics, Biology and MedicineOnline ISSN 1352-8661Print ISSN 0968-5243
	
		Journal Volume Volume 22
	
		Journal Issue Volume 22, Number 4 / August, 2009
	
]]></description>
</item>

<item rdf:about="http://www.springerlink.com/content/9l57472rx3607275/">
<title>Detection and quantification of d-glucuronic acid in human bile using 1H NMR spectroscopy: relevance to the diagnosis of pancreatic cancer</title>
<link>http://www.springerlink.com/content/9l57472rx3607275/</link>
<description><![CDATA[Abstract
 Objective&nbsp;&nbsp;There are no specific biomarkers available for the definitive diagnosis of pancreatic cancer. Analysis of d-glucuronic acid (GlcUA) in bile could be valuable in this regard.
 
 
 
 Materials and methods&nbsp;&nbsp;Bile samples obtained from patients with pancreatic cancer (n = 4), chronic pancreatitis (n = 3) and control patients with biliary obstruction (n = 10) were analyzed by 1H NMR spectroscopy. GlcUA was quantified from the peak area of the α-1CH signal (at 5.24&nbsp;ppm) obtained by deconvolution.
 
 
 
 Results&nbsp;&nbsp;GlcUA was detected in human bile by one-dimensional 1H NMR and two-dimensional 1H–1H COSY and TOCSY experiments. Quantification of GlcUA was achieved by measuring the peak area of the α-1CH signal using CPMG experiment, and the quantities of GlcUA were calibrated to account for the attenuation due to T
 2 relaxation. GlcUA was observed at elevated levels in bile samples obtained from pancreatic cancer patients, whereas it was
 either absent or found in negligible amounts in control and chronic pancreatitis patients. The reason for the presence of
 elevated levels of GlcUA could be the hydrolysis of biliary bilirubin diglucuronide by β-glucuronidase, released excessively from pancreatic tissue during the course of malignancy.
 
 
 
 Conclusion&nbsp;&nbsp;Analysis of d-glucuronic acid in bile could be valuable in the detection of pancreatic cancer, and detecting GlcUA by in vivo 1H MRS has the potential to help in the non-invasive diagnosis of pancreatic cancer. Given that only four cancer patients have
 been studied so far, the new biomarker is regarded as a preliminary finding, but one that warrants further investigation.
 
 
 
	Content Type Journal ArticleCategory Research ArticleDOI 10.1007/s10334-009-0171-5Authors
		Tedros Bezabeh, National Research Council Institute for Biodiagnostics 435 Ellice Avenue Winnipeg MB R3B 1Y6 CanadaOmkar B. Ijare, National Research Council Institute for Biodiagnostics 435 Ellice Avenue Winnipeg MB R3B 1Y6 CanadaNils Albiin, CLINTEC, Karolinska Institutet Division of Radiology Stockholm SwedenUrban Arnelo, CLINTEC, Karolinska Institutet Division of Surgery Stockholm SwedenBo Lindberg, CLINTEC, Karolinska Institutet Division of Radiology Stockholm SwedenIan C. P. Smith, National Research Council Institute for Biodiagnostics 435 Ellice Avenue Winnipeg MB R3B 1Y6 Canada
	

	
		Journal Magnetic Resonance Materials in Physics, Biology and MedicineOnline ISSN 1352-8661Print ISSN 0968-5243
	
		Journal Volume Volume 22
	
		Journal Issue Volume 22, Number 5 / October, 2009
	
]]></description>
</item>

<item rdf:about="http://www.springerlink.com/content/t455842k3h132313/">
<title>Extraction of the first bolus passage in dynamic susceptibility contrast perfusion measurements</title>
<link>http://www.springerlink.com/content/t455842k3h132313/</link>
<description><![CDATA[Abstract
 Object&nbsp;&nbsp;The processing of dynamic susceptibility contrast perfusion measurements requires an extraction of the first bolus passage
 of the injected contrast agent. State-of-the-art methods employ the fit of a gamma variate function to the measured data.
 The use of a gamma variate function is motivated by its shape similarity to the expected relaxation rate time-course during
 the first bolus passage. However, the quality of this result is strongly influenced by the amount of overlap of the first
 and second bolus passage. In this work we present an alternative, data-driven method for the extraction of the first bolus
 passage from a measured relaxation time-course.
 
 
 
 Materials and methods&nbsp;&nbsp;By using prior knowledge of the injection function, the measured time-courses can be transformed to time-courses that would
 occur at a shorter injection duration where the two bolus passages have less overlap. This time-course is found by Tikhonov
 regularized deconvolution of the measured time-courses with an injection function that bases on the measurement protocol.
 A minimum search yields the cut-off point at which the first bolus can be extrapolated to zero. The gamma variate fit is performed
 using Powells algorithm. The proposed approach is compared to the gamma variate fit approach using simulations and an exemplary
 dataset from one healthy volunteer.
 
 
 
 Results&nbsp;&nbsp;The new method performs comparably stable as the gamma variate function fit approach in simulations. Both methods are superior
 to a simple exponential extrapolation approach. Applied to volunteer data, the new method performs much faster than the gamma
 variate fit approach. The results obtained from both methods correspond well.
 
 
 
 Conclusion&nbsp;&nbsp;The new method offers a conceptual understanding of the first bolus passage and yields similar results to the gamma variate
 function fit approach but performs much faster.
 
 
 
	Content Type Journal ArticleCategory Research ArticleDOI 10.1007/s10334-009-0170-6Authors
		Peter Gall, University Medical Center Freiburg Department of Diagnostic Radiology, Medical Physics Hugstetterstrasse 55 79106 Freiburg GermanyIrina Mader, University Medical Center Freiburg Department of Neuroradiology Breisacher Strasse 64 79106 Freiburg GermanyValerij G. Kiselev, University Medical Center Freiburg Department of Diagnostic Radiology, Medical Physics Hugstetterstrasse 55 79106 Freiburg Germany
	

	
		Journal Magnetic Resonance Materials in Physics, Biology and MedicineOnline ISSN 1352-8661Print ISSN 0968-5243
	
		Journal Volume Volume 22
	
		Journal Issue Volume 22, Number 4 / August, 2009
	
]]></description>
</item>

<item rdf:about="http://www.springerlink.com/content/g3208q031773h306/">
<title>Fast multiecho balanced SSFP metabolite mapping of 1H and hyperpolarized 13C compounds</title>
<link>http://www.springerlink.com/content/g3208q031773h306/</link>
<description><![CDATA[Abstract
 Object&nbsp;&nbsp;To investigate the feasibility of multiecho balanced steady-state free precession (bSSFP)-based fast chemical shift mapping
 hyperpolarized 13C metabolites. The overall goal was to reduce total imaging time and to increase spatial resolution compared to common chemical
 shift imaging (CSI).
 
 
 
 Materials and methods&nbsp;&nbsp;A multiecho bSSFP sequence in combination with an iterative reconstruction algorithm was implemented. 1H experiments were performed on phantoms and on a human volunteer in order to investigate the feasibility of the method on
 a system with metabolite maps that are known beforehand. 13C experiments were performed in vivo on pigs, where CSI images were acquired also for comparison.
 
 
 
 Results&nbsp;&nbsp;Chemical shift images of three and four distinct 1H resonance frequencies as well as chemical shift images of up to five hyperpolarized 13C metabolites were successfully obtained.
 
 
 
 Conclusion&nbsp;&nbsp;Fast metabolite mapping based on multiecho balanced SSFP in combination with an iterative reconstruction approach could successfully
 separate several 1H resonances and hyperpolarized 13C metabolites.
 
 
 
	Content Type Journal ArticleCategory Research ArticleDOI 10.1007/s10334-009-0169-zAuthors
		Jochen Leupold, University Hospital Freiburg Department of Diagnostic Radiology, Medical Physics Freiburg GermanySven Månsson, Lund University, Malmö University Hospital Medical Radiation Physics and Radiology, Department of Clinical Sciences Malmö Malmö SwedenJ. Stefan Petersson, GE Healthcare Helsingborg SwedenJürgen Hennig, University Hospital Freiburg Department of Diagnostic Radiology, Medical Physics Freiburg GermanyOliver Wieben, University of Wisconsin-Madison Departments of Medical Physics and Radiology, Wisconsin Institutes for Medical Research (WIMR) 1111 Highland Ave. Madison WI 53705-2275 USA
	

	
		Journal Magnetic Resonance Materials in Physics, Biology and MedicineOnline ISSN 1352-8661Print ISSN 0968-5243
	
		Journal Volume Volume 22
	
		Journal Issue Volume 22, Number 4 / August, 2009
	
]]></description>
</item>

<item rdf:about="http://www.springerlink.com/content/d15734v644n1538q/">
<title>Voxel-based reproducibility of T2 relaxation time in patellar cartilage at 1.5 T with a new validated 3D rigid registration algorithm</title>
<link>http://www.springerlink.com/content/d15734v644n1538q/</link>
<description><![CDATA[Abstract
 Object&nbsp;&nbsp;T2 relaxation time is a promising MRI parameter for the early diagnosis and follow-up of osteoarthritis. Assessing the evolution
 of osteoarthritis needs exact comparison of datasets acquired at different times and knowledge of the T2 reproducibility.
 The aims of this work were to establish a method for voxel-wise comparison of T2 datasets and to assess voxel-based T2 reproducibility
 in healthy patellar cartilage.
 
 
 
 Materials and methods&nbsp;&nbsp;A new rigid 3D-registration algorithm was developed. The precision of the registration algorithm was calculated with numerical
 simulations and in vitro measurements. In vivo T2 reproducibility was assessed in six volunteers measured at seven different
 times. The voxel-based reproducibility was characterized with the coefficient of variation (CV) of T2, and its regional variations
 were analyzed.
 
 
 
 Results&nbsp;&nbsp;The registration algorithm showed an average registration precision lower than 25% of the voxel size. In vivo voxel-based
 T2 reproducibility exhibited a median CV of 10.1%. Reproducibility showed significant regional differences. Largest CVs (15.4%)
 were found near the articular surface. The central regions showed the lowest CVs (7.2%) and the lateral regions intermediate
 CVs (11.2%).
 
 
 
 Conclusion&nbsp;&nbsp;Using a rigid 3D-registration algorithm provides voxel-based T2 reproducibility errors comparable to former, 2D region-based
 approaches, thus opening the possibility of voxel-based monitoring of cartilage degradation in osteoarthritis.
 
 
 
	Content Type Journal ArticleCategory Research ArticleDOI 10.1007/s10334-009-0168-0Authors
		José G. Raya, Ludwig Maximilian University of Munich Josef Lissner Laboratory for Biomedical Imaging, Department of Clinical Radiology, Großhadern Marchioninistr. 15 81377 Munich GermanyAnnie Horng, Ludwig Maximilian University of Munich Department of Clinical Radiology, Großhadern Munich GermanyOlaf Dietrich, Ludwig Maximilian University of Munich Josef Lissner Laboratory for Biomedical Imaging, Department of Clinical Radiology, Großhadern Marchioninistr. 15 81377 Munich GermanyJürgen Weber, Ludwig Maximilian University of Munich Josef Lissner Laboratory for Biomedical Imaging, Department of Clinical Radiology, Großhadern Marchioninistr. 15 81377 Munich GermanyJulia Dinges, Klinikum rechts der Isar der Technischen Universität München Institut für Röntgendiagnostik Munich GermanyElisabeth Mützel, Ludwig Maximilian University of Munich Department of Forensic Medicine Munich GermanyMaximilian F. Reiser, Ludwig Maximilian University of Munich Josef Lissner Laboratory for Biomedical Imaging, Department of Clinical Radiology, Großhadern Marchioninistr. 15 81377 Munich GermanyChristian Glaser, Ludwig Maximilian University of Munich Department of Clinical Radiology, Großhadern Munich Germany
	

	
		Journal Magnetic Resonance Materials in Physics, Biology and MedicineOnline ISSN 1352-8661Print ISSN 0968-5243
	
		Journal Volume Volume 22
	
		Journal Issue Volume 22, Number 4 / August, 2009
	
]]></description>
</item>

<item rdf:about="http://www.springerlink.com/content/y16054151084n601/">
<title>Design of internal MRI coils using ultimate intrinsic SNR</title>
<link>http://www.springerlink.com/content/y16054151084n601/</link>
<description><![CDATA[Abstract
 Object&nbsp;&nbsp;Internal MRI coils have important applications in diagnostic and interventional studies. Since they can be placed very close
 to the region of interest in the body, they are favored over external coils in applications where high-resolution images are
 required. In this paper it is demonstrated that ultimate intrinsic SNR (UISNR) and the optimum coil sensitivity solutions
 can be used to make new coil designs with higher intrinsic SNR.
 
 
 
 Materials and methods&nbsp;&nbsp;In this study, UISNR, which is the maximum attainable value of the intrinsic SNR, is used as a measure of performance and
 as a design criterion. As an example, a novel endorectal MRI coil is designed. The design is tested with phantom and patient
 studies.
 
 
 
 Results&nbsp;&nbsp;An endorectal coil is built to demonstrate the effectiveness of the design strategy. ISNR of the endorectal coil approximates
 the UISNR to 72%.
 
 
 
 Conclusion&nbsp;&nbsp;An internal coil design method that takes advantage of the UISNR and optimum coil sensitivity calculations was presented.
 This method can also be used to design better internal MRI coils for different applications.
 
 
 
	Content Type Journal ArticleCategory Research ArticleDOI 10.1007/s10334-009-0167-1Authors
		Yiğitcan Eryaman, Bilkent University Department of Electrical and Electronics Engineering 06800 Ankara TurkeyYusuf Öner, Gazi University Department of Radiology Ankara TurkeyErgin Atalar, Bilkent University Department of Electrical and Electronics Engineering 06800 Ankara Turkey
	

	
		Journal Magnetic Resonance Materials in Physics, Biology and MedicineOnline ISSN 1352-8661Print ISSN 0968-5243
	
		Journal Volume Volume 22
	
		Journal Issue Volume 22, Number 4 / August, 2009
	
]]></description>
</item>

<item rdf:about="http://www.springerlink.com/content/m35741r1661m4180/">
<title>Metabolic changes in the rat brain after a photochemical lesion treated by stem cell transplantation assessed by 1H MRS</title>
<link>http://www.springerlink.com/content/m35741r1661m4180/</link>
<description><![CDATA[Abstract
 Object&nbsp;&nbsp;Metabolite changes in an experimental lesion in the rat cortex and in the contralateral hemisphere after the intravenous administration
 of mesenchymal stem cells (MSCs) were assessed by proton MR spectroscopy to verify the impact of the cell treatment on the
 brain tissue.
 
 
 
 Materials and methods&nbsp;&nbsp;Wistar rats with a photochemical cortical lesion and transplanted MSCs or sham transplanted rats were examined. Proton spectra
 were obtained from the lesion and from the contralateral cortex.
 
 
 
 Results&nbsp;&nbsp;Magnetic resonance spectroscopy revealed a gradual recovery of the damaged tissue; however, we found no significant differences
 in metabolite concentrations in the lesioned hemisphere between treated and untreated animals. Higher concentrations of glutamate
 and N-acetyl aspartate were found in the contralateral hemisphere in cell-treated animals compared to untreated ones. Lesioned
 animals showed neurogenesis in the contralateral hemisphere; the number of newly generated cells in stem cell-treated animals
 was 50% higher than those observed in untreated animals.
 
 
 
 Conclusion&nbsp;&nbsp;No direct impact of cell transplantation was observed in the lesion. However, changes in the contralateral hemisphere suggest
 that the transplanted MSCs might stimulate repair processes and plasticity resulting in the generation of newborn cells, which
 might enable the faster adoption of the damaged tissue’s function by healthy tissue.
 
 
 
	Content Type Journal ArticleCategory Research ArticleDOI 10.1007/s10334-009-0166-2Authors
		Vít Herynek, Institute for Clinical and Experimental Medicine MR-Unit, Department of Radiodiagnostic and Interventional Radiology Vídeňská 1958/9 140 21 Prague Czech RepublicKateřina Růžičková, Charles University Center for Cell Therapy and Tissue Repair, Second Medical Faculty V Úvalu 84 150 06 Prague Czech RepublicPavla Jendelová, Charles University Center for Cell Therapy and Tissue Repair, Second Medical Faculty V Úvalu 84 150 06 Prague Czech RepublicEva Syková, Charles University Center for Cell Therapy and Tissue Repair, Second Medical Faculty V Úvalu 84 150 06 Prague Czech RepublicMilan Hájek, Institute for Clinical and Experimental Medicine MR-Unit, Department of Radiodiagnostic and Interventional Radiology Vídeňská 1958/9 140 21 Prague Czech Republic
	

	
		Journal Magnetic Resonance Materials in Physics, Biology and MedicineOnline ISSN 1352-8661Print ISSN 0968-5243
	
		Journal Volume Volume 22
	
		Journal Issue Volume 22, Number 4 / August, 2009
	
]]></description>
</item>

</rdf:RDF>