Gradient moment nulling used as motion artifact suppression technique (MAST) reduces constant velocity motion distortion in standard spin echo or gradient echo pulse sequences. It is an adjustment to zero at the echo time (TE) of the net moments of the amplitude of the waveform of the magnetic field gradients with time. The zeroth moment is the area under the curve. The first moment is the 'center of gravity' etc.
The aim is to minimize the phase shifts acquired by the transverse magnetization of excited nuclei moving along the gradients (including the effect of refocusing radio frequency pulses), particularly for the reduction of image artifacts due to motion.

(GMR) The application of strategic gradient pulses can compensate the objectionable spin phase effects of flow motion. That means the reducing of flow effects, e.g. gradient moment nulling of the first order of flow. The simplest velocity-compensated pulse sequence is the symmetrical second echo of a spin echo pulse sequence.
Gradient field changes can be configured in such a way that during an echo the magnetization signal vectors for all pixels have zero phase angle independent of velocities, accelerations etc. of the measured tissue. E.g. the adjustment to zero at the time TE of the net moments of the amplitude of the waveform of the magnetic field gradients with time. The zeroth moment is the area under the curve, the first moment is the 'center of gravity' etc. The aim is to minimize the phase shifts acquired by the transverse magnetization of excited nuclei moving along the gradients (including the effect of refocusing RF pulses), particularly for the reduction of image artifacts due to motion.
Also called Flow Compensation (FC), Motion Artifact Suppression Technique (MAST), Flow motion compression (STILL), Gradient Rephasing (GR), Shimadzu Motion Artifact Reduction Technique (SMART).

(MRA) Magnetic resonance angiography is a medical imaging technique to visualize blood filled structures, including arteries, veins and the heart chambers. This MRI technique creates soft tissue contrast between blood vessels and surrounding tissues primarily created by flow, rather than displaying the vessel lumen. There are bright blood and black blood MRA techniques, named according to the appearance of the blood vessels. With this different MRA techniques both, the blood flow and the condition of the blood vessel walls can be seen. Flow effects in MRI can produce a range of artifacts. MRA takes advantage of these artifacts to create predictable image contrast due to the nature of flow.
Technical parameters of the MRA sequence greatly affect the sensitivity of the images to flow with different velocities or directions, turbulent flow and vessel size.
This are the three main types of MRA:
All angiographic techniques differentially enhance vascular MR signal. The names of the bright blood techniques TOF and PCA reflect the physical properties of flowing blood that were exploited to make the vessels appear bright. Contrast enhanced magnetic resonance angiography creates the angiographic effect by using an intravenously administered MR contrast agent to selectively shorten the T1 of blood and thereby cause the vessels to appear bright on T1 weighted images.
MRA images optimally display areas of constant blood flow-velocity, but there are many situations where the flow within a voxel has non-uniform speed or direction. In a diseased vessel these patterns are even more complex. Similar loss of streamline flow occurs at all vessel junctions and stenoses, and in regions of mural thrombosis. It results in a loss of signal, due to the loss of phase coherence between spins in the voxel.
This signal loss, usually only noticeable distal to a stenosis, used to be an obvious characteristic of MRA images. It is minimized by using small voxels and the shortest possible TE. Signal loss from disorganized flow is most noticeable in TOF imaging but also affects the PCA images.
Indications to perform a magnetic resonance angiography (MRA):
Conventional angiography or computerized tomography angiography (CT angiography) may be needed after MRA if a problem (such as an aneurysm) is present or if surgery is being considered.

See also Magnetic Resonance Imaging MRI.

Magnetic forces are fundamental forces that arise due to the movement of electrical charge. Maxwell's equations describe the origin and behavior of the fields that govern these forces. Thus, magnetism is seen whenever electrically charged particles are in motion. This can arise either from movement of electrons in an electric current, resulting in 'electromagnetism', or from the quantum-mechanical orbital motion (there is no orbital motion of electrons around the nucleus like planets around the sun, but there is an 'effective electron velocity') and spin of electrons, resulting in what are known as 'permanent magnets'.
The physical cause of the magnetism of objects, as distinct from electrical currents, is the atomic magnetic dipole. Magnetic dipoles, or magnetic moments, result on the atomic scale from the two kinds of movement of electrons. The first is the orbital motion of the electron around the nucleus this motion can be considered as a current loop, resulting in an orbital dipole magnetic moment along the axis of the nucleus. The second, much stronger, source of electronic magnetic moment is due to a quantum mechanical property called the spin dipole magnetic moment.
Gauss (G) and tesla (T) are units to define the intensity of magnetic fields. One tesla is equivalent to 10 000 gauss.
Typically, the field strength of MRI scanners is between 0.15 T and 3 T.

See also Diamagnetism, Paramagnetism, Superparamagnetism, and Ferromagnetism.

This effect is an additional electrical charge generated by ions in blood (loaded particles) moving perpendicular to the magnetic field. At 1.5 T, no significant changes are expected; at 6.0 T a 10% blood pressure change is expected. A blood pressure increase is predicted theoretically for a field of 10 T. This is claimed to be caused by interaction of induced electrical potentials and currents within a solution, e.g. blood, and an electrical volume force causing a retardation in the direction opposite to the fluid flow. This decrease in blood flow-velocity must be compensated for by an elevation in pressure.
Static magnetic field gradients of 0.01 T/cm (100 G/cm) make no significant difference in the membrane transport processes. The influence of a static magnetic field upon erythrocytes is not sufficient to provoke sedimentation, as long as there is a normal blood circulation.

The magnetohydrodynamic effect which results from a voltage occurring across a vessel in a magnetic field, is irrelevant at the field strengths used.