The sensitive point in an object (or a region) is the point from which information is being measured, as in sequential point imaging or in single voxel MR spectroscopy sequential point imaging used. To define a sensitive point, it must be selected in three dimensions. Different combinations of selective excitation, inversion, or saturation pulses can be used. Sometimes, combinations of two or more measurements are necessary to define the sensitive point (or volume).

See also Magnetic Resonance Spectroscopy.

Sequential line imaging technique utilizing two orthogonal oscillating magnetic field gradients, a SFP pulse sequence, and signal averaging to isolate the NMR spectrometer sensitivity to a desired line in the body.

MR imaging techniques in which the image is built from successive point positions in the object. In various schemes, the points are isolated by oscillating magnetic field gradients (sensitive point) or shaped magnetic fields.

(MIP) MRA images can be processed by Maximum Intensity Projection to interactively create different projections. The MIP connects the high intensity dots of the blood vessels in three dimensions, providing an angiogram that can be viewed from any projection. Each point in the MIP represents the highest intensity experienced in that location on any partition within the imaging volume.
For complete interpretation the base slices should also be reviewed individually and with multiplanar reconstruction (MPR) software. The MIP can then be displayed in a CINE format or filmed as multiple images acquired from different projections. Although the maximum intensity projection (MIP) algorithm is sensitive to high signal from inflowing spins, it is also sensitive to high signal of any other etiology.

(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.