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Result : Searchterm 'Saturation Recovery' found in 1 term [] and 4 definitions [], (+ 8 Boolean[] results
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(SPIR) A specialized technique that selectively saturates fat protons prior to acquiring data as in standard sequences, so that they produce a negligible signal. The presaturation pulse is applied prior to each slice selection. This technique requires a very homogeneous magnetic field and very precise frequency calibration. | | | | | | | | | | | Further Reading: | Basics:
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From ONI Medical Systems, Inc.;
MSK-Extreme™ MRI system is a dedicated high field extremity imaging device, designed to provide orthopedic surgeons and other physicians with detailed diagnostic images of the foot, ankle, knee, hand, wrist and elbow, all with the clinical confidence and advantages derived from high field, whole body MRI units. The light weight (less than 650 kg) of the OrthOne System performs rapid patient studies, is easy to operate, has a patient friendly open environment and can be installed in a practice office or hospital, all at a cost similar to a low field extremity machine.
New features include a more powerful operating system that offers increased scan speed as well as a 160-mm knee coil with higher signal to noise ratio, and the option of a CD burner.
Device Information and Specification 16 cm knee, 18 cm lower extremity;; 12.3 cm upper extremity, additional high resolution v-SPEC Coils: 80 mm, 100 mm, or 145 mm. SE, FSE, GE2D, GE3D, Inversion recovery (IR), Driven Equilibrium, Fat Saturation (FS), STIR, MT, PD, Flow Compensation (FC), RF spoiling, MTE, No Phase Wrap (NPW) IMAGING MODES Scout, single, multislice, volume 2D less than 200 msec/image X/Y: 64-512; 2 pixel steps 4,096 grey lvls; 256 lvls in 3D POWER REQUIREMENTS 115VAC, 1phase, 20A; 208VAC, 3 phase, 30A COOLING SYSTEM TYPE LHe with 2 stage cold head 1.25m radial x 1.8m axial
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'Next generation MRI system 1.5T CHORUS developed by ISOL Technology is optimized for both clinical diagnostic imaging and for research development.
CHORUS offers the complete range of feature oriented advanced imaging techniques- for both clinical routine and research. The compact short bore magnet, the patient friendly design and the gradient technology make the innovation to new degree of perfection in magnetic resonance.'
Device Information and Specification
CLINICAL APPLICATION
Whole body
Spin Echo, Gradient Echo, Fast Spin Echo,
Inversion Recovery ( STIR, Fluid Attenuated Inversion Recovery), FLASH, FISP, PSIF, Turbo Flash ( MPRAGE ),TOF MR Angiography, Standard echo planar imaging package (SE-EPI, GE-EPI), Optional:
Advanced P.A. Imaging Package (up to 4 ch.), Advanced echo planar imaging package,
Single Shot and Diffusion Weighted EPI, IR/FLAIR EPI
STRENGTH
20 mT/m (Upto 27 mT/m)
| | | | • View the DATABASE results for 'CHORUS 1.5T™' (2).
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Quick Overview Please note that there are different common names for this artifact.
DESCRIPTION
Black or bright band
During frequency encoding, fat protons precess slower than water protons in the same slice because of their magnetic shielding. Through the difference in resonance frequency between water and fat, protons at the same location are misregistrated (dislocated) by the Fourier transformation, when converting MRI signals from frequency to spatial domain. This chemical shift misregistration cause accentuation of any fat-water interfaces along the frequency axis and may be mistaken for pathology. Where fat and water are in the same location, this artifact can be seen as a bright or dark band at the edge of the anatomy.
Protons in fat and water molecules are separated by a chemical shift of about 3.5 ppm. The actual shift in Hertz (Hz) depends on the magnetic field strength of the magnet being used. Higher field strength increases the misregistration, while in contrast a higher gradient strength has a positive effect. For a 0.3 T system operating at 12.8 MHz the shift will be 44.8 Hz compared with a 223.6 Hz shift for a 1.5 T system operating at 63.9 MHz.
Image Guidance
| | | | • View the DATABASE results for 'Chemical Shift Artifact' (7).
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(CSI) Chemical shift imaging is an extension of MR spectroscopy, allowing metabolite information to be measured in an extended region and to add the chemical analysis of body tissues to the potential clinical utility of Magnetic Resonance. The spatial location is phase encoded and a spectrum is recorded at each phase encoding step to allow the spectra acquisition in a number of volumes covering the whole sample. CSI provides mapping of chemical shifts, analog to individual spectral lines or groups of lines.
Spatial resolution can be in one, two or three dimensions, but with long acquisition times od full 3D CSI. Commonly a slice-selected 2D acquisition is used. The chemical composition of each voxel is represented by spectra, or as an image in which the signal intensity depends on the concentration of an individual metabolite. Alternatively frequency-selective pulses excite only a single spectral component.
There are several methods of performing chemical shift imaging, e.g. the inversion recovery method, chemical shift selective imaging sequence, chemical shift insensitive slice selective RF pulse, the saturation method, spatial and chemical shift encoded excitation and quantitative chemical shift imaging.
See also Magnetic Resonance Spectroscopy. | | | | • View the DATABASE results for 'Chemical Shift Imaging' (6).
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