Home About us Contact
|
Home About us Contact | ||
|
|
||
Isotropic Spatial Resolution (isotropic + spatial_resolution)
Selected Abstracts3D diffusion tensor MRI with isotropic resolution using a steady-state radial acquisitionJOURNAL OF MAGNETIC RESONANCE IMAGING, Issue 5 2009Youngkyoo Jung PhD Abstract Purpose To obtain diffusion tensor images (DTI) over a large image volume rapidly with 3D isotropic spatial resolution, minimal spatial distortions, and reduced motion artifacts, a diffusion-weighted steady-state 3D projection (SS 3DPR) pulse sequence was developed. Materials and Methods A diffusion gradient was inserted in a SS 3DPR pulse sequence. The acquisition was synchronized to the cardiac cycle, linear phase errors were corrected along the readout direction, and each projection was weighted by measures of consistency with other data. A new iterative parallel imaging reconstruction method was also implemented for removing off-resonance and undersampling artifacts simultaneously. Results The contrast and appearance of both the fractional anisotropy and eigenvector color maps were substantially improved after all correction techniques were applied. True 3D DTI datasets were obtained in vivo over the whole brain (240 mm field of view in all directions) with 1.87 mm isotropic spatial resolution, six diffusion encoding directions in under 19 minutes. Conclusion A true 3D DTI pulse sequence with high isotropic spatial resolution was developed for whole brain imaging in under 20 minutes. To minimize the effects of brain motion, a cardiac synchronized, multiecho, DW-SSFP pulse sequence was implemented. Motion artifacts were further reduced by a combination of linear phase correction, corrupt projection detection and rejection, sampling density reweighting, and parallel imaging reconstruction. The combination of these methods greatly improved the quality of 3D DTI in the brain. J. Magn. Reson. Imaging 2009;29:1175,1184. © 2009 Wiley-Liss, Inc. [source] Magnetic Resonance Microscopy Defines Ethanol-Induced Brain Abnormalities in Prenatal Mice: Effects of Acute Insult on Gestational Day 7ALCOHOLISM, Issue 1 2010Elizabeth A. Godin Background:, This magnetic resonance microscopy (MRM)-based report is the second in a series designed to illustrate the spectrum of craniofacial and central nervous system (CNS) dysmorphia resulting from single- and multiple-day maternal ethanol treatment. The study described in this report examined the consequences of ethanol exposure on gestational day (GD) 7 in mice, a time in development when gastrulation and neural plate development begins; corresponding to the mid- to late third week postfertilization in humans. Acute GD 7 ethanol exposure in mice has previously been shown to result in CNS defects consistent with holoprosencephaly (HPE) and craniofacial anomalies typical of those in Fetal Alcohol Syndrome (FAS). MRM has facilitated further definition of the range of GD 7 ethanol-induced defects. Methods:, C57Bl/6J female mice were intraperitoneally (i.p.) administered vehicle or 2 injections of 2.9 g/kg ethanol on day 7 of pregnancy. Stage-matched control and ethanol-exposed GD 17 fetuses selected for imaging were immersion fixed in a Bouins/Prohance solution. MRM was conducted at either 7.0 Tesla (T) or 9.4 T. Resulting 29 ,m isotropic spatial resolution scans were segmented and reconstructed to provide 3D images. Linear and volumetric brain measures, as well as morphological features, were compared for control and ethanol-exposed fetuses. Following MRM, selected specimens were processed for routine histology and light microscopic examination. Results:, Gestational day 7 ethanol exposure resulted in a spectrum of median facial and forebrain deficiencies, as expected. This range of abnormalities falls within the HPE spectrum; a spectrum for which facial dysmorphology is consistent with and typically is predictive of that of the forebrain. In addition, other defects including median facial cleft, cleft palate, micrognathia, pituitary agenesis, and third ventricular dilatation were identified. MRM analyses also revealed cerebral cortical dysplasia/heterotopias resulting from this acute, early insult and facilitated a subsequent focused histological investigation of these defects. Conclusions:, Individual MRM scans and 3D reconstructions of fetal mouse brains have facilitated demonstration of a broad range of GD 7 ethanol-induced morphological abnormality. These results, including the discovery of cerebral cortical heterotopias, elucidate the teratogenic potential of ethanol insult during the third week of human prenatal development. [source] Time-resolved bolus-chase MR angiography with real-time triggering of table motionMAGNETIC RESONANCE IN MEDICINE, Issue 3 2010Casey P. Johnson Abstract Time-resolved bolus-chase contrast-enhanced MR angiography with real-time station switching is demonstrated. The Cartesian acquisition with projection reconstruction-like sampling (CAPR) technique and high 2D sensitivity encoding (SENSE) (6× or 8×) and 2D homodyne (1.8×) accelerations were used to acquire 3D volumes with 1.0-mm isotropic spatial resolution and frame times as low as 2.5 sec in two imaging stations covering the thighs and calves. A custom real-time system was developed to reconstruct and display CAPR frames for visually guided triggering of table motion upon passage of contrast through the proximal station. The method was evaluated in seven volunteers. High-spatial-resolution arteriograms with minimal venous contamination were consistently acquired in both stations. Real-time stepping table contrast-enhanced MR angiography is a method for providing time-resolved images with high spatial resolution over an extended field-of-view. Magn Reson Med, 2010. © 2010 Wiley-Liss, Inc. [source] Quantitative sodium imaging with a flexible twisted projection pulse sequenceMAGNETIC RESONANCE IN MEDICINE, Issue 6 2010Aiming Lu Abstract The quantification of sodium MR images from an arbitrary intensity scale into a bioscale fosters image interpretation in terms of the spatially resolved biochemical process of sodium ion homeostasis. A methodology for quantifying tissue sodium concentration using a flexible twisted projection imaging sequence is proposed that allows for optimization of tradeoffs between readout time, signal-to-noise ratio efficiency, and sensitivity to static field susceptibility artifacts. The gradient amplitude supported by the slew rate at each k -space radius regularizes the readout gradient waveform design to avoid slew rate violation. Static field inhomogeneity artifacts are corrected using a frequency-segmented conjugate phase reconstruction approach, with field maps obtained quickly from coregistered proton imaging. High-quality quantitative sodium images have been achieved in phantom and volunteer studies with real isotropic spatial resolution of 7.5 × 7.5 × 7.5 mm3 for the slow T2 component in ,8 min on a clinical 3-T scanner. After correcting for coil sensitivity inhomogeneity and water fraction, the tissue sodium concentration in gray matter and white matter was measured to be 36.6 ± 0.6 ,mol/g wet weight and 27.6 ± 1.2 ,mol/g wet weight, respectively. Magn Reson Med 63:1583,1593, 2010. © 2010 Wiley-Liss, Inc. [source] 3D fluoroscopy with real-time 3D non-cartesian phased-array contrast-enhanced MRA,MAGNETIC RESONANCE IN MEDICINE, Issue 2 2006Ethan Brodsky Abstract For optimized CE-MRA of the chest and abdomen, the scan time and breath-hold must be coordinated with the arrival of contrast. A 3D fluoroscopy system is demonstrated that performs real-time 3D projection reconstruction acquisition, reconstruction, and visualization using only the standard scanner hardware and operator console workstation. Unlike 2D fluorotriggering techniques, no specification of a monitoring slab or careful placement of the imaging volume is required. 3DPR data are acquired continuously throughout the examination using an eight-channel receiver and 1 s interleaved subframes. The data are reconstructed using 1 s segments for real-time monitoring with 0.8-cm isotropic spatial resolution over the entire torso, allowing full-volume axial, coronal, and sagittal MIPs to be displayed simultaneously with minimal latency. The system later uses the same scan data to generate high-spatial-resolution time-resolved sequences of the breath-hold interval. The 3D fluoroscopy system was validated on phantoms and human volunteers. Magn Reson Med, 2006. © 2006 Wiley-Liss, Inc. [source] Fibonacci grids: A novel approach to global modellingTHE QUARTERLY JOURNAL OF THE ROYAL METEOROLOGICAL SOCIETY, Issue 619 2006Richard Swinbank Abstract Recent years have seen a resurgence of interest in a variety of non-standard computational grids for global numerical prediction. The motivation has been to reduce problems associated with the converging meridians and the polar singularities of conventional regular latitude,longitude grids. A further impetus has come from the adoption of massively parallel computers, for which it is necessary to distribute work equitably across the processors; this is more practicable for some non-standard grids. Desirable attributes of a grid for high-order spatial finite differencing are: (i) geometrical regularity; (ii) a homogeneous and approximately isotropic spatial resolution; (iii) a low proportion of the grid points where the numerical procedures require special customization (such as near coordinate singularities or grid edges); (iv) ease of parallelization. One family of grid arrangements which, to our knowledge, has never before been applied to numerical weather prediction, but which appears to offer several technical advantages, are what we shall refer to as ,Fibonacci grids'. These grids possess virtually uniform and isotropic resolution, with an equal area for each grid point. There are only two compact singular regions on a sphere that require customized numerics. We demonstrate the practicality of this type of grid in shallow-water simulations, and discuss the prospects for efficiently using these frameworks in three-dimensional weather prediction or climate models. © Crown copyright, 2006. Royal Meteorological Society [source] Optimizing the point spread function in phase-encoded magnetic resonance microscopyCONCEPTS IN MAGNETIC RESONANCE, Issue 1 2004A.G. Webb Abstract Three-dimensional phase-encoded magnetic resonance microscopy is the most promising method for obtaining images with isotropic spatial resolutions on the order of a few micrometers. The attainable spatial resolution is limited by the available gradient strength (Gmax) and the molecular self-diffusion coefficient (D) of the sample. In this study, numerical simulations in the microscopic-size regime are presented in order to show that for given values of Gmax and D, there exists an optimum number of phase-encoding steps that maximize the spatial resolution in terms of minimizing the full-width at half-maximum (FWHM) of the image point spread function (PSF). Unlike the case of "macroscopic" imaging, in which diffusion plays an insignificant role in determining spatial resolution, acquiring data beyond this optimal value actually degrades the image PSF. An alternative version of phase encoding, using a variable phase-encoding time rather than a variable gradient strength, is analyzed in terms of improvements in the image PSF and/or reductions in the data acquisition time for a given spatial resolution. © 2004 Wiley Periodicals, Inc. Concepts Magn Reson 22A: 25,36, 2004. [source] | ||||||||||