Abstract: A method for performing spectroscopy using an interleaved readout for at least two species. A B0 field is applied. A first spatial-spectral (SPSP) position resolved spectroscopy sequence (PRESS) excitation with a sufficiently narrow band to excite a first species without exciting a second species is applied. A first readout that measures the first species is performed. A second SPSP PRESS excitation with a sufficiently narrow band to excite the second species without exciting the first species is applied. A second readout that measures the second species is performed.

Abstract: A method for frequency selective and slice selective magnetic resonance imaging (MRI) is provided. A B0 field is applied. A self-refocused spatial-spectral (SPSP) RF pulse is applied. A readout of a portion of k-space for the excited slice is performed. A second self-refocused SPSP excitation RF pulse is applied, wherein the second self-refocused SPSP excitation has an 180° echo phase difference from the self-refocused SPSP excitation. A second readout of a portion of k-space for the excited slice was performed. A difference between the readout and the second readout was found. The previous steps were repeated until k-space has been filled for the excited slice. The previous steps were repeated for a plurality of slices.

Abstract: A method of imaging the individual components of systems with sparse spectra using magnetic resonance imaging including the steps of a) exciting nuclei of labeled components using a MRI pulse sequence, b) selecting a proper spectral window to avoid/minimize signal overlap of aliased frequency components. In step a) preferably a spiral chemical shift imaging (spCSI) sequence is employed. In a preferred embodiment, hyperpolarized nuclei of 13C are used for labeling in a pyruvate substrate with metabolites of lacatate, alanine, and bicarbonate.

Abstract: A manifestation of the invention provides a method for slice selective excitation for magnetic resonance imaging (MRI). A B0 field is applied. A STABLE pulse comprising of a BIR-4 envelope sampled by a plurality of subpulses with a duration is applied, where amplitude and frequency modulation functions of the BIR-4 envelope are slowly varying with respect to the duration of the subpulses. A portion of k-space is read out to obtain k-space data. The STABLE pulse and readout are repeated until sufficient k-space has been acquired. A Fourier Transform of the k-space data is taken.

Abstract: A method for frequency selective and slice selective magnetic resonance imaging (MRI) is provided. A B0 field is applied. A self-refocused spatial-spectral (SPSP) RF pulse is applied. A readout of a portion of k-space for the excited slice is performed. A second self-refocused SPSP excitation RF pulse is applied, wherein the second self-refocused SPSP excitation has an 180° echo phase difference from the self-refocused SPSP excitation. A second readout of a portion of k-space for the excited slice was performed. A difference between the readout and the second readout was found. The previous steps were repeated until k-space has been filled for the excited slice. The previous steps were repeated for a plurality of slices.

Abstract: A manifestation of the invention provides a method for slice selective excitation for magnetic resonance imaging (MRI). A B0 field is applied. A STABLE pulse comprising of a BIR-4 envelope sampled by a plurality of subpulses with a duration is applied, where amplitude and frequency modulation functions of the BIR-4 envelope are slowly varying with respect to the duration of the subpulses. A portion of k-space is read out to obtain k-space data. The STABLE pulse and readout are repeated until sufficient k-space has been acquired. A Fourier Transform of the k-space data is taken.

Abstract: A method for performing spectroscopy using an interleaved readout for at least two species. A B0 field is applied. A first spatial-spectral (SPSP) position resolved spectroscopy sequence (PRESS) excitation with a sufficiently narrow band to excite a first species without exciting a second species is applied. A first readout that measures the first species is performed. A second SPSP PRESS excitation with a sufficiently narrow band to excite the second species without exciting the first species is applied. A second readout that measures the second species is performed.

Abstract: A method of imaging the individual components of systems with sparse spectra using magnetic resonance imaging including the steps of a) exciting nuclei of labeled components using a MRI pulse sequence, b) selecting a proper spectral window to avoid/minimize signal overlap of aliased frequency components. In step a) preferably a spiral chemical shift imaging (spCSI) sequence is employed. In a preferred embodiment, hyperpolarized nuclei of 13C are used for labeling in a pyruvate substrate with metabolites of lacatate, alanine, and bicarbonate.