(TEeff) The contrast and the SNR of an MR image are determined primarily by the temporal position of the echo at which the phase encoding gradient has the smallest amplitude. The echo signal in this case undergoes minimal dephasing and has the strongest signal. The time period between the excitation pulse and this echo is the effective echo time.

(FA) The flip angle a is used to define the angle of excitation for a field echo pulse sequence. It is the angle to which the net magnetization is rotated or tipped relative to the main magnetic field direction via the application of a RF excitation pulse at the Larmor frequency. It is also referred to as the tip angle, nutation angle or angle of nutation.
The radio frequency power (which is proportional to the square of the amplitude) of the pulse is proportional to a through which the spins are tilted under its influence. Flip angles between 0° and 90° are typically used in gradient echo sequences, 90° and a series of 180° pulses in spin echo sequences and an initial 180° pulse followed by a 90° and a 180° pulse in inversion recovery sequences.

Quantification relies on inflow effects or on spin phase effects and therefore on quantifying the phase shifts of moving tissues relative to stationary tissues.
With properly designed pulse sequences (see phase contrast sequence) the pixel by pixel phase represents a map of the velocities measured in the imaging plane. Spin phase effect-based flow quantification schemes use pulse sequences specifically designed so that the phase angle in a pixel obtained upon measuring the signal is proportional to the velocity. As the relation of the phase angle to the velocity is defined by the gradient amplitudes and the gradient switch-on times, which are known, velocity can be determined quantitatively on a pixel-by-pixel basis. Once, this velocity is known, the flow in a vessel can be determined by multiplying the pixel area with the pixel velocity. Summing this quantity for all pixels inside a vessel results in a flow volume, which is measured, e.g. in ml/sec.
Flow related enhancement-based flow quantification techniques (entry phenomena) work because spins in a section perpendicular to the vessel of interest are labeled with some radio frequency RF pulse. Positional readout of the tagged spins some time T later will show the distance D they have traveled.
For constant flow, the velocity v is obtained by dividing the distance D by the time T : v = D/T. Variations of this basic principle have been proposed to measure flow, but the standard methods to measure velocity and flow use the spin phase effect.
Cardiac MRI sequences are used to encode images with velocity information. These pulse sequences permit quantification of flow-related physiologic data, such as blood flow in the aorta or pulmonary arteries and the peak velocity across stenotic valves.

(FT) The Fourier transformation is a mathematical procedure to separate out the frequency components of a signal from its amplitudes as a function of time, or the inverse Fourier transformation (IFT) calculates the time domain from the frequency domain. The FT is used to generate the spectrum from the free induction decay or spin echo in the pulse MR technique and is essential to most MR imaging techniques. The Fourier transformation can be generalized to multiple dimensions, e.g. to relate an image to its corresponding k-space representation, or to include chemical shift information in some chemical shift imaging techniques. Fourier transformation analysis allows spatial information to be reconstructed from the raw data.

(FID) A free induction decay curve is generated as excited nuclei relax. The amplitude of the FID signal becomes smaller over time as net magnetization returns to equilibrium. If transverse magnetization of the spins is produced, e.g. by a 90° pulse, a transient MR signal will result that will decay toward zero with a characteristic time constant T2 (or T2*); this decaying signal is the free induction decay.
The signal peaks of the echoes fall onto this T2 decay curve, while at each echo the signals arise and decay with T2*. The typical T2 relaxation times being of the order of 5-200 ms in the human body. The first part of the FID is not observable (named the 'receiver dead time') caused by residual effects of the powerful exciting radio frequency pulse on the electronics of the receiver.