(GRAPPA) GRAPPA is a parallel imaging technique to speed up MRI pulse sequences. The Fourier plane of the image is reconstructed from the frequency signals of each coil (reconstruction in the frequency domain).
Parallel imaging techniques like GRAPPA, auto-SMASH and VD-AUTO-SMASH are second and third generation algorithms using k-space undersampling. A model from a part of the center of k-space is acquired, to find the coefficients of the signals from each coil element, and to reconstruct the missing intermediary lines. The acquisition of these additional lines is a form of self-calibration, which lengthens the overall short scan time. The acquisition of these k-space lines provides mapping of the whole field as well as data for the image contrast.
Algorithms of the GRAPPA type work better than the SENSE type in heterogeneous body parts like thoracic or abdominal imaging, or in pulse sequences like echo planar imaging. This is caused by differences between the sensitivity map and the pulse sequence (e.g. artifacts) or an unreliable sensitivity map.

(HASTE) A pulse sequence with data acquisition after an initial preparation pulse for contrast enhancement with the use of a very long echo train (Single shot TSE), whereat each echo is individually phase encoded. This technique is a heavily T2 weighted, high speed sequence with partial Fourier technique, a great sensitivity for fluid detection and a fast acquisition time of about 1 sec per slice. This advantage makes it possible for using breath-hold with excellent motionless MRI, e.g. used for liver and lung imaging.

See also Segmented HASTE.

(HS) A method in which approximately one half of the acquisition matrix in the phase encoding direction is acquired. Half scan is possible because of symmetry in acquired data. Since negative values of phase encoded measurements are identical to corresponding positive values, only a little over half (more than 62.5%) of a scan actually needs to be acquired to replicate an entire scan. This results in a reduction in scan time at the expense of signal to noise ratio. The time reduction can be nearly a factor of two, but full resolution is maintained.
Half scan can be used when scan times are long, the signal to noise ratio is not critical and where full spatial resolution is required. Half scan is particularly appropriate for scans with a large field of view and relatively thick slices; and, in 3D scans with many slices. In some fast scanning techniques the use of Half scan enables a shorter TE thus improving contrast. For this reason, the Half scan parameter is located in the contrast menu.

More information about scan time reduction; see also partial fourier technique.

(MP-GRE / MPRAGE / MP-RAGE) A fast 3D gradient echo pulse sequence using a magnetization preparation pulse like TurboFLASH. Only one segment or partition of a 3D data record is obtained per inversion preparation pulse. After the acquisition, for all rows a delay time (TD) is used to prevent saturation effects.
MPRAGE is designed for rapid acquisition with T1 weighted dominance. Fast gradient echoes are characterized by their rapid sampling time, high signal intensity and image contrast while approaching steady state (the echo is collected during the time when tissues are experiencing T1 relaxation). The rapid speed of the acquisition makes it an excellent alternative to breath-hold abdominal imaging, neuro, dynamic bolus, MR angiography and cardiac imaging.

See Gradient Echo Sequence.

(PC) Phase contrast sequences are the basis of MRA techniques utilizing the change in the phase shifts of the flowing protons in the region of interest to create an image. Spins that are moving along the direction of a magnetic field gradient receive a phase shift proportional to their velocity.
In a phase contrast sequence two data sets with a different amount of flow sensitivity are acquired. This is usually accomplished by applying gradient pairs, which sequentially dephase and then rephase spins during the sequence. Both 2D and 3D acquisition techniques can be applied with phase contrast MRA.
The first data set is acquired with a flow compensated sequence, i. e. without flow sensitivity. The second data set is acquired with a flow sensitive sequence. The amount of flow sensitivity is controlled by the strength of the bipolar gradient pulse pair, which is incorporated into the sequence. Stationary tissue undergoes no effective phase change after the application of the two gradients. Caused by the different spatial localization of flowing blood to stationary tissue, it experiences a different size of the second bipolar gradient compared to the first. The result is a phase shift.
The raw data from the two data sets are subtracted. By comparing the phase of signals from each location in the two sequences the exact amount of motion induced phase change can be determined to have a map where pixel brightness is proportional to spatial velocity.
Phase contrast images represent the signal intensity of the velocity of spins at each point within the field of view. Regions that are stationary remain black while moving regions are represented as grey to white.
The phase shift is proportional to the spin's velocity, and this allows the quantitative assessment of flow velocities. The difference MRI signal has a maximum value for opposite directions. This velocity is typically referred to as venc, and depends on the pulse amplitude and distance between the gradient pulse pair. For velocities larger than venc the difference signal is decreased constantly until it gets zero. Therefore, in a phase contrast angiography it is important to correctly set the venc of the sequence to the maximum flow velocity which is expected during the measurement. High venc factors of the PC angiogram (more than 40 cm/sec) will selectively image the arteries (PCA - arteriography), whereas a venc factor of 20 cm/sec will perform the veins and sinuses (PCV or MRV - venography).

See also Flow Quantification, Contrast Enhanced MR Venography, Time of Flight Angiography, Time Resolved Imaging of Contrast Kinetics.