Volumetric imaging is a 3D technique where all the MRI signals are collected from the entire tissue sample and imaged as a whole entity, therefore providing a high signal to noise ratio. The acquisition of isotropic voxels or thin slices with high spatial resolution allows to create multiplanar reconstructions in all planes; a compensation for the usually longer scan time. The acquisition time can be reduced by parallel imaging technique.
New T2 weighted variants of 3D sequences (FSE-XETA, T2-SPACE, VISTA) have been introduced that differ from conventional FSE sequences. An echo train containing up to 200 echoes obtained at a minimum echo spacing allows very fast acquisition. A flip angle modulation (flip angle sweep - FAS) during the FSE readout carries magnetization as long as possible to avoid blurring and provide optimal signal at the effective echo time. This type of imaging is well suited for brain and spine MRI procedures.
Newer T1 weighted variants include Liver Acquisition with Volume Acquisition (LAVA) and T1W High Resolution Isotropic Volume Examination (THRIVE), which have advantages for dynamic breath hold imaging in liver and abdominal examinations.

See also Volume Imaging, 3 Dimensional Imaging.

From Siemens Medical Systems; Received FDA clearance in 2013.
The MAGNETOM Prisma is the 3T PowerPack for exploration that offers most demanding clinical and research challenges of today and the future. The latest parallel transmit technology, TimTX TrueShape, enables zooming into specific body regions for enhanced image quality. Furthermore, the Tim 4G integrated coil technology offers remarkable imaging flexibility and supports complex examinations across the whole body.
Onsite upgrades to the MAGNETOM Prisma for customers who have already installed the 3 Tesla MAGNETOM Trio are possible.

Quick Overview
Please note that there are different common names for this artifact.

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.

For artifact reduction helps a smaller water fat shift (higher bandwidth), a higher matrix, an in phase TE or a spin echo technique. Since the misregistration offset is present in the read out axis the patient may be rescanned with this axis parallel to the fat-water interface. Steeper gradient may be employed to reduce the chemical shift offset in mm. Another strategy is to employ specialized pulse sequences such as fat saturation or inversion recovery imaging. Fat suppression techniques eliminate chemical shift artifacts caused by the lack of fat signal.

See also Black Boundary Artifact and Magnetic Resonance Spectroscopy.

(TOF) The time of flight angiography is used for the imaging of vessels. Usually the sequence type is a gradient echo sequences with short TR, acquired with slices perpendicular to the direction of blood flow.
The source of diverse flow effects is the difference between the unsaturated and presaturated spins and creates a bright vascular image without the invasive use of contrast media. Flowing blood moves unsaturated spins from outside the slice into the imaging plane. These completely relaxed spins have full equilibrium magnetization and produce (when entering the imaging plane) a much higher signal than stationary spins if a gradient echo sequence is generated. This flow related enhancement is also referred to as entry slice phenomenon, or inflow enhancement.
Performing a presaturation slab on one side parallel to the slice can selectively destroy the MR signal from the in-flowing blood from this side of the slice. This allows the technique to be flow direction sensitive and to separate arteriograms or venograms. When the local magnetization of moving blood is selectively altered in a region, e.g. by selective excitation, it carries the altered magnetization with it when it moves, thus tagging the selected region for times on the order of the relaxation times.
For maximum flow signal, a complete new part of blood has to enter the slice every repetition (TR) period, which makes time of flight angiography sensitive to flow-velocity. The choice of TR and slice thickness should be appropriate to the expected flow-velocities because even small changes in slice thickness influences the performance of the TOF sequence. The use of sequential 2 dimensional Fourier transformation (2DFT) slices, 3DFT slabs, or multiple 3D slabs (chunks) are depending on the coverage required and the range of flow-velocities.
3D TOF MRA is routinely used for evaluating the Circle of Willis.

See also Magnetic Resonance Angiography and Contrast Enhanced Magnetic Resonance Angiography.

A tomographic imaging plane, parallel to the ground, perpendicular (rotated 90°) to the long axis of the human body; the axial plane separates the superior from the inferior part (the head from the feet).
Also called transaxial, transversal, transverse plane.