(PRESS) Point resolved spectroscopy is a multi echo single shot technique to obtain spectral data. PRESS is a 90°-180°-180° (slice selective pulses) sequence. The 90° radio frequency pulse rotates the spins in the yx-plane, followed by the first 180° pulse (spin rotation in the xz-plane) and the second 180° pulse (spin rotation in the xy-plane), which gives the signal.
With the long echo times used in PRESS, there is a better visualization of metabolites with longer relaxation times. Many of the metabolites depicted by stimulated echo technique are not seen on point resolved spectroscopy, but PRESS is less susceptible to motion, diffusion, and quantum effects and has a better SNR than stimulated echo acquisition mode (STEAM).

In the last years, cardiac MRI techniques have progressively improved. No other noninvasive imaging modality provides the same degree of contrast and temporal resolution for the assessment of cardiovascular anatomy and pathology. Contraindications MRI are the same as for other magnetic resonance techniques.
The primary advantage of MRI is extremely high contrast resolution between different tissue types, including blood. Moreover, MRI is a true 3 dimensional imaging modality and images can be obtained in any oblique plane along the true cardiac axes while preserving high temporal and spatial resolution with precise demonstration of cardiac anatomy without the administration of contrast media.
Due to these properties, MRI can precisely characterize cardiac function and quantify cavity volumes, ejection fraction, and left ventricular mass. In addition, cardiac MRI has the ability to quantify flow (see flow quantification), including bulk flow in vessels, pressure gradients across stenosis, regurgitant fractions and shunt fractions. Valve morphology and area can be determined and the severity of stenosis quantified. In certain disease states, such as myocardial infarction, the contrast resolution of MRI is further improved by the addition of extrinsic contrast agents (see myocardial late enhancement).
A dedicated cardiac coil, and a field strength higher than 1 Tesla is recommended to have sufficient signal. Cardiac MRI acquires ECG gating. Cardiac gating (ECGs) obtained within the MRI scanner, can be degraded by the superimposed electrical potential of flowing blood in the magnetic field. Therefore, excellent contact between the skin and ECG leads is necessary. For male patients, the skin at the lead sites can be shaved. A good cooperation of the patient is necessary because breath holding at the end of expiration is practiced during the most sequences.

See also Displacement Encoding with Stimulated Echoes.
For Ultrasound Imaging (USI) see Cardiac Ultrasound at Medical-Ultrasound-Imaging.com.

See also the related poll results: 'In 2010 your scanner will probably work with a field strength of' and 'MRI will have replaced 50% of x-ray exams by'

The selective excitation of spins in only a limited region of space. This can be particularly useful for spectroscopy as well as imaging. Spatial localization of the signal source may be achieved through spatially selective excitation and the resulting signal may be analyzed directly for the spectrum corresponding to the excited region. It is usually achieved with selective excitation.
Typically, a single dimension of localization can be achieved with one selective RF excitation pulse (and a magnetic field gradient along a desired direction), while a localized volume (3D) can be excited with a stimulated echo produced with three selective RF pulses whose selective magnetic field gradients are mutually orthogonal, having a common intersection in the desired region. Similar 'crossed plane' excitation can be used with selective 180° refocusing pulses and conventional spin echoes.
A degree of spatial localization of excitation can alternatively be achieved with depth pulses, e.g. when using surface coils for excitation as well as signal detection. An indirect application of selective excitation for volume-selected spectroscopy is to use appropriate combinations of signals acquired after selective inversion of different regions, in order to subtract away the signal from undesired regions.

(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.