The application of 3D radial sampling of the free-induction decay to proton ultrashort echo-time (UTE) imaging is reported. The effects of T 2 decay during signal acquisition on the 3D radial point-spread function are analyzed and compared to 2D radial and 1D sampling. It is found that in addition to the use of ultrashort TE, the proper choice of the acquisition-window duration T AQ is essential for imaging short-T 2 components. For 3D radial sampling, a maximal signal-to-noise ratio (

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Balanced FFE offers a potential alternative for endogenous contrast enhancement in navigator-gated free-breathing 3D coronary MRA. The obtained results together with the relatively short scanning time warrant further studies in larger patient collectives.

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Experimental procedures for obtaining localized 31P NMR spectra of humans by means of the ISIS sequence are discussed in detail. The technique is optimized for use with volume coils and with surface coils in order to measure localized 31P NMR spectra of different tissues and organs. Selective frequency-modulated (FM) inversion and excitation pulses are applied for optimal inversion or excitation despite B1 inhomogeneity. Pulse imperfection may lead to spurious signal contributions from outside the selected volume; this contamination is reduced by using long pulse intervals, by properly ordering the ISIS acquisitions, and by using FM excitation pulses. Simultaneous measurement of multiple volumes was implemented by including an additional selective inversion pulse, and an extension of the ISIS addition/subtraction scheme. Localized T1 measurements with surface coils are implemented by using a B1-insensitive inversion pulse in the inversion recovery sequence. The quantitative reproducibility of localized 31P NMR spectra was verified. Absolute metabolite concentration can be determined after a suitable calibration of the 31P NMR spectrum. Localized shimming is required to obtain localized 31P NMR spectra of excellent spectral resolution. This is done by monitoring the 1H NMR signal from water by a single-shot localization technique. The techniques discussed can be applied to obtain spectra of brain, liver, heart, and other organs. 31P NMR spectra of intracranial tumors demonstrate its applicability in the examination of patients.

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A new method for fast magnetic resonance imaging is presented. It provides a more rapid data acquisition than two-dimensional Fourier imaging (2DFI) by a factor which may be chosen depending on the required signal-to-noise ratio of the image. In addition to the readout gradient of 2DFI, the present method employs an oscillating modulation gradient. In this way, a curved alternating trajectory in k space is sampled after each spin excitation. For a p-times accelerated data acquisition, the trajectory consists of p periods, where p is of the order of 2 to 8 for low-frequency gradient modulation but can be chosen higher if certain hardware requirements are met. Adequate sampling density in k space is obtained by scanning shifted trajectories after subsequent spin excitations. The method can be combined with volume imaging (3DFI) and multiple slice 2DFI. It was implemented on a standard Philips Gyroscan system without any hardware modifications. Results obtained for an acceleration factor p = 4 are shown.