(CISS) This gradient echo sequence is a stimulated T2 echo. Two TrueFISP sequences are acquired with differing RF pulses and than combined for strong T2 Weighted high resolution 3D images.
These TrueFISP sequences are normally affected by dark phase dispersion bands, which are caused by patient induced local field inhomogeneities and made prominent by the relatively long TR used. The different excitation pulse regimes offset these bands in the 2 sequences. Combining the images results in a picture free of banding. The image combination is performed automatically after data collection, adding some time to the reconstruction process. The advantage of the 3D CISS sequence is its combination of high signal levels and extremely high spatial resolution.
Used for, e.g. inner ear, cranial nerves and cerebellum.

See also Steady State Free Precession.

(CE-FAST) In this technique, the MR signal is sampled immediately prior to each RF pulse. Because the signal is formed by a true spin echo, its contrast is predominantly T2-, rather than T2*-based and is less sensitive to artifacts and signal losses related to field non-uniformity and susceptibility variation. While the signal to noise ratio is limited, the CE-FAST method has the advantage of good contrast.

See Contrast Enhanced Gradient Echo Sequence and Gradient Echo Sequence.

(PDWI) In density weighted imaging, the contrast is dependent on the density of protons in the tissue. Proton density weighted images are generated by choosing TR greater than T1 (typically ≥ 2 000 ms) and TE less than T2 (typically ≤ 30 ms), the two exponential terms are both close to one and therefore M is relatively independent of T1 and T2, thereby emphasizing Mxy0, which is proportional to the proton density. Also called (Rho) ρ-weighted.

See also Proton Density Weighted Image.

Short name: Dy-DOTA-4AmCE, central moiety: Dy2+, contrast effect: T2*enhanced
Dy-DOTA-4AmCE, a macrocyclic complex is characterized by a very slow water exchange, a complex compared with several Dy-DTPA derivatives known for their efficacy as T2 contrast agents at high magnetic fields.

(FISP) A fast imaging sequence, which attempts to combine the signals observed separately in the FADE sequence, generally sensitive about magnetic susceptibility artifacts and imperfections in the gradient waveforms. Confusingly now often used to refer to a refocused FLASH type sequence.
This sequence is very similar to FLASH, except that the spoiler pulse is eliminated. As a result, any transverse magnetization still present at the time of the next RF pulse is incorporated into the steady state. FISP uses a RF pulse that alternates in sign. Because there is still some remaining transverse magnetization at the time of the RF pulse, a RF pulse of a degree flips the spins less than a degree from the longitudinal axis. With small flip angles, very little longitudinal magnetization is lost and the image contrast becomes almost independent of T1. Using a very short TE (with TR 20-50 ms, flip angle 30-45°) eliminates T2* effects, so that the images become proton density weighted. As the flip angle is increased, the contrast becomes increasingly dependent on T1 and T2*. It is in the domain of large flip angles and short TR that FISP exhibits vastly different contrast to FLASH type sequences. Used for T1 orthopedic imaging, 3D MPR, cardiography and angiography.