(STIR) Also called Short Tau (t) (inversion time) Inversion Recovery. STIR is a fat suppression technique with an inversion time t = T1 ln2 where the signal of fat is zero (T1 is the spin lattice relaxation time of the component that should be suppressed). To distinguish two tissue components with this technique, the T1 values must be different. Fluid Attenuation Inversion Recovery (FLAIR) is a similar technique to suppress water.
Inversion recovery doubles the distance spins will recover, allowing more time for T1 differences. A 180° preparation pulse inverts the net magnetization to the negative longitudinal magnetization prior to the 90° excitation pulse. This specialized application of the inversion recovery sequence set the inversion time (t) of the sequence at 0.69 times the T1 of fat. The T1 of fat at 1.5 Tesla is approximately 250 with a null point of 170 ms while at 0.5 Tesla its 215 with a 148 ms null point. At the moment of excitation, about 120 to 170 ms after the 180° inversion pulse (depending of the magnetic field) the magnetization of the fat signal has just risen to zero from its original, negative, value and no fat signal is available to be flipped into the transverse plane.
When deciding on the optimal T1 time, factors to be considered include not only the main field strength, but also the tissue to be suppressed and the anatomy. In comparison to a conventional spin echo where tissues with a short T1 are bright due to faster recovery, fat signal is reversed or darkened. Because body fluids have both a long T1 and a long T2, it is evident that STIR offers the possibility of extremely sensitive detection of body fluid. This is of course, only true for stationary fluid such as edema, as the MRI signal of flowing fluids is governed by other factors.

See also Fat Suppression and Inversion Recovery Sequence.

In single shot techniques (used for EPI, TSE, FSE, RARE, HASTE), the entire raw data set is acquired with a single excitation pulse. The magnetization of a fully relaxed spin system is used. Each of the subsequent echoes is given a different phase encoding. For improved SNR, spatial resolution or FOV, the needed raw data are acquired over a number of sequence repetitions. Each repetition then collects a fraction of the complete raw data set. Only slightly more than a half of the raw data is acquired. The image is obtained through half Fourier reconstruction.
A single shot sequence is useful in cases where movement is to expect e.g. in abdominal Imaging or fetal MRI.

See also Half Fourier Acquisition Single Shot Turbo Spin Echo.

A form of a spin echo produced by three pulse RF sequences, consisting of two RF pulses following an initial exciting RF pulse. The stimulated echo appears at a time delay after the third pulse equal to the interval between the first two pulses. Although classically produced with 90° pulses, any RF pulses other than an ideal 180° can produce a stimulated echo. The intensity of the echo depends in part on the T1 relaxation time because the excitation is 'stored' as longitudinal magnetization between the second and third RF pulses. For example, use of stimulated echoes with spatially selective excitation with orthogonal magnetic field gradients permits volume-selective excitation for spectroscopic localization.

Artifacts may appear as a series of fine lines. A narrow bandwidth causes a wide read window, which allows the stimulated echo to be incorporated into the image data. This can be supported by increasing the received bandwidth, which would narrow the read window, thus not incorporating the extraneous echo. Another help would be to change the first echo time, which may change the spacing of the stimulated echoes to outside that of the read window for the second echo.

(T2* or T two star) The observed time constant of the FID due to loss of phase coherence among spins oriented at an angle to the static magnetic field. Commonly due to a combination of magnetic field inhomogeneities, dB, and spin spin transverse relaxation, with the result of rapid loss in transverse magnetization and MRI signal. MRI signals can usually still be recovered as a spin echo in times less than or on the order of T2.
1/T2 * @ 1/T2 + Dw/2; Dw = gDB. The FID will generally not be exponential, so that T2* will not be unique.

(τ) The interpulse times (time between the 90° and 180° pulse, and between the 180° pulse and the echo) used in a spin echo pulse sequence.