(bFFE) A FFE sequence using a balanced gradient waveform. A balanced sequence starts out with a RF pulse of 90° or less and the spins in the steady state. Before the next TR in the slice phase and frequency encoding, gradients are balanced so their net value is zero. Now the spins are prepared to accept the next RF pulse, and their corresponding signal can become part of the new transverse magnetization. Since the balanced gradients maintain the transverse and longitudinal magnetization, the result is, that both T1 and T2 contrast are represented in the image. This pulse sequence produces images with increased signal from fluid, along with retaining T1 weighted tissue contrast. Because this form of sequence is extremely dependent on field homogeneity, it is essential to run a shimming prior the acquisition. A fully balanced (refocused) sequence would yield higher signal, especially for tissues with long T2 relaxation times.

See Steady State Free Precession and Gradient Echo Sequence.

(BW) Bandwidth is a measure of frequency range, the range between the highest and lowest frequency allowed in the signal. For analog signals, which can be mathematically viewed as a function of time, bandwidth is the width, measured in Hertz of a frequency range in which the signal's Fourier transform is nonzero.

A higher bandwidth is used for the reduction of chemical shift artifacts (lower bandwidth - more chemical shift - longer dwell time - but better signal to noise ratio). Narrow receive bandwidths accentuate this water fat shift by assigning a smaller number of frequencies across the MRI image. This effect is much more significant on higher field strengths. At 1.5 T, fat and water precess 220 Hz apart, which results in a higher shift than in Low Field MRI.
Lower bandwidth (measured in Hz) = higher water fat shift (measured in pixel shift).

See also Aliasing, Aliasing Artifact, Frequency Encoding, and Chemical Shift Artifact.

(CSI) Chemical shift imaging is an extension of MR spectroscopy, allowing metabolite information to be measured in an extended region and to add the chemical analysis of body tissues to the potential clinical utility of Magnetic Resonance. The spatial location is phase encoded and a spectrum is recorded at each phase encoding step to allow the spectra acquisition in a number of volumes covering the whole sample. CSI provides mapping of chemical shifts, analog to individual spectral lines or groups of lines.
Spatial resolution can be in one, two or three dimensions, but with long acquisition times od full 3D CSI. Commonly a slice-selected 2D acquisition is used. The chemical composition of each voxel is represented by spectra, or as an image in which the signal intensity depends on the concentration of an individual metabolite. Alternatively frequency-selective pulses excite only a single spectral component.
There are several methods of performing chemical shift imaging, e.g. the inversion recovery method, chemical shift selective imaging sequence, chemical shift insensitive slice selective RF pulse, the saturation method, spatial and chemical shift encoded excitation and quantitative chemical shift imaging.

See also Magnetic Resonance Spectroscopy.

(Gφ) The phase encoding gradient is a magnetic field gradient that allows the encoding of the spatial signal location along a second dimension by different spin phases. The phase encoding gradient is applied after slice selection and excitation (before the frequency encoding gradient), orthogonally to the other two gradients. The spatial resolution is directly related to the number of phase encoding steps (gradients).

(HS) A method in which approximately one half of the acquisition matrix in the phase encoding direction is acquired. Half scan is possible because of symmetry in acquired data. Since negative values of phase encoded measurements are identical to corresponding positive values, only a little over half (more than 62.5%) of a scan actually needs to be acquired to replicate an entire scan. This results in a reduction in scan time at the expense of signal to noise ratio. The time reduction can be nearly a factor of two, but full resolution is maintained.
Half scan can be used when scan times are long, the signal to noise ratio is not critical and where full spatial resolution is required. Half scan is particularly appropriate for scans with a large field of view and relatively thick slices; and, in 3D scans with many slices. In some fast scanning techniques the use of Half scan enables a shorter TE thus improving contrast. For this reason, the Half scan parameter is located in the contrast menu.

More information about scan time reduction; see also partial fourier technique.