A type of magnet that utilizes the principles of electromagnetism to generate the magnetic field. Typically large current values and significant cooling of the magnet coils is required. The resistive magnet does not require cryogens, but needs a constant power supply to maintain a homogenous magnetic field, and can be quite expensive to maintain.
Resistive magnets fall into two general categories - iron-core and air-core.
Iron-core electromagnets provide the advantages of a vertically oriented magnetic field, and a limited fringe field with little, if any, missile effects due to the closed iron-flux return path.
Air-core electromagnets exhibit horizontally oriented fields, which have large fringe fields (unless magnetically shielded) and are prone to missile effects. Resistive magnets are typically limited to maximum field strengths of approximately 0.6T.

Respiratory compensation reduces motion artifacts due to breathing. The approach is to reassign the echoes that are sensitive to respiratory motion in the central region of k-space. The outer lines of phase encoding normally contain the echoes where the motion from expiration is the greatest. The central portion of k-space will have encoded the echoes where inspiration and expiration are minimal. By a bellows device fixed to the abdomen, monitoring of the diaphragm excursion is possible. Respiratory compensation does not increase scan time with most systems.
An advantage of very fast sequences is the possibility of breath holding during the acquisition to eliminate motion artifacts. Breath hold is commonly used on most abdominal studies where images are acquired using gradient echo-based sequences during a brief inspiratory period (20-30 seconds). To enhance the breath holding endurance of the patient, connecting the patient to oxygen at a 1-liter flow rate via a nasal cannula has been shown to be helpful.
Also called PEAR, Respiratory Trigger, Respiratory Gating, PRIZE, FREEZE, Phase Reordering.

See also Phase Encoding Artifact Reduction, Respiratory Ordered Phase Encoding.

(SENSE) A MRI technique for relevant scan time reduction. The spatial information related to the coils of a receiver array are utilized for reducing conventional Fourier encoding. In principle, SENSE can be applied to any imaging sequence and k-space trajectories. However, it is particularly feasible for Cartesian sampling schemes. In 2D Fourier imaging with common Cartesian sampling of k-space sensitivity encoding by means of a receiver array enables to reduce the number of Fourier encoding steps.
SENSE reconstruction without artifacts relies on accurate knowledge of the individual coil sensitivities. For sensitivity assessment, low-resolution, fully Fourier-encoded reference images are required, obtained with each array element and with a body coil.
The major negative point of parallel imaging techniques is that they diminish SNR in proportion to the numbers of reduction factors. R is the factor by which the number of k-space samples is reduced. In standard Fourier imaging reducing the sampling density results in the reduction of the FOV, causing aliasing. In fact, SENSE reconstruction in the Cartesian case is efficiently performed by first creating one such aliased image for each array element using discrete Fourier transformation (DFT).
The next step then is to create a full-FOV image from the set of intermediate images. To achieve this one must undo the signal superposition underlying the fold-over effect. That is, for each pixel in the reduced FOV the signal contributions from a number of positions in the full FOV need to be separated. These positions form a Cartesian grid corresponding to the size of the reduced FOV.
The advantages are especially true for contrast-enhanced MR imaging such as dynamic liver MRI (liver imaging) , 3 dimensional magnetic resonance angiography (3D MRA), and magnetic resonance cholangiopancreaticography (MRCP).
The excellent scan speed of SENSE allows for acquisition of two separate sets of hepatic MR images within the time regarded as the hepatic arterial-phase (double arterial-phase technique) as well as that of multidetector CT.
SENSE can also increase the time efficiency of spatial signal encoding in 3D MRA. With SENSE, even ultrafast (sub second) 4D MRA can be realized.
For MRCP acquisition, high-resolution 3D MRCP images can be constantly provided by SENSE. This is because SENSE resolves the presence of the severe motion artifacts due to longer acquisition time. Longer acquisition time, which results in diminishing image quality, is the greatest problem for 3D MRCP imaging.
In addition, SENSE reduces the train of gradient echoes in combination with a faster k-space traversal per unit time, thereby dramatically improving the image quality of single shot echo planar imaging (i.e. T2 weighted, diffusion weighted imaging).

(SVS) This method maps the metabolic information from the VOI in a spectrum. Single volume techniques are advantageous in case of pathological changes that cannot spatially be limited to a few VOI; by using local volume sensitive shim the local magnetic field inhomogeneity can be compensated.

(USPIO) The class of the ultrasmall superparamagnetic iron oxide includes several chemically and pharmacologically very distinct materials, which may or may not be interchangeable for a specific use. Some ultrasmall SPIO particles (median diameter less than 50nm) are used as MRI contrast agents (Sinerem®, Combidex®), e.g. to differentiate metastatic from inflammatory lymph nodes. USPIO shows also potential for providing important information about angiogenesis in cancer tumors and could possibly complement MRI helping physicians to identify dangerous arteriosclerosis plaques.
Because of the disadvantageous large T2*//T1 ratio, USPIO compounds are less suitable for arterial bolus contrast enhanced magnetic resonance angiography than gadolinium complexes. The tiny ultrasmall superparamagnetic iron oxides do not accumulate in the RES system as fast as larger particles, which results in a long plasma half-life. USPIO particles, with a small median diameter (less than 10 nm), will accumulate in lymph nodes after an intravenous injection by e.g. direct transcapillary passage through endothelial venules. Once within the nodal parenchyma, phagocytic cells of the mononuclear phagocyte system take up the particles.
As a second way, USPIOs are subsequently taken up from then interstitium by lymphatic vessels and transported to regional lymph nodes. A lymph node with normal phagocytic function takes up a considerable amount and shows a reduction of the signal intensity caused by T2 shortening effects and magnetic susceptibility. Caused by the small uptake of the USPIOs in metastatic lymph nodes, they appear with less signal reduction, and permit the differentiation of healthy lymph nodes from normal-sized, metastatic nodes.

See also Superparamagnetic Contrast Agents, Superparamagnetic Iron Oxide, Very Small Superparamagnetic Iron Oxide Particles, Blood Pool Agents, Intracellular Contrast Agents.