A Time-of-flight (TOF) MRI scanning method may include: a TOF MRI scan including a first slice selection gradient applied in the Z direction at the same time as an RF pulse being applied to an imaging target; after applying the RF pulse and first slice selection gradient has ended, applying a slice selection encoding gradient and a phase encoding gradient in the Z direction and Y direction respectively; when application of the slice selection encoding gradient and phase encoding gradient ends, applying a readout gradient in the X direction; when application of the readout gradient ends, applying a tracking saturation pulse to the imaging target, and simultaneously applying a second slice selection gradient in the Z direction; when application of the tracking saturation pulse ends, applying a spoiler gradient in the X, Y and/or Z directions of the magnetic field. The method advantageously reduces the TOF MRI scanning time.

A magnetic resonance imaging apparatus according to an embodiment includes sequence controlling circuitry and processing circuitry. The sequence controlling circuitry is configured to execute (i) a first pulse sequence in which a spatially selective Inversion recovery (IR) pulse and a spatially non-selective IR pulse are applied, and subsequently an acquisition is performed and (ii) a second pulse sequence in which the spatially non-selective IR pulse is applied without applying the spatially selective IR pulse, and subsequently an acquisition is performed, while varying the first TI period, with respect to a plurality of first TI periods. The processing circuitry is configured to calculate a second TI period to be used in a third pulse sequence and a fourth pulse sequence, based on data obtained from the first pulse sequence and the second pulse sequence. The sequence controlling circuitry executes (iii) the third pulse sequence in which the spatially selective IR pulse and the spatially non-selective IR pulse are applied, and subsequently an acquisition is performed and (iv) the fourth pulse sequence in which the spatially non-selective IR pulse is applied without applying the spatially selective IR pulse, and subsequently an acquisition is performed. The processing circuitry generates a magnetic resonance image of an imaged region based on data obtained from the third pulse sequence and the fourth pulse sequence.

The present application provides a system and method for using a nuclear magnetic resonance (NMR) system. The method includes performing a pulse sequence using the NMR system that spatially encodes NMR signal evolutions to be acquired from a subject using an aggregated radio-frequency (B1) field incoherence and resolving the NMR signal evolutions acquired from the subject using at least one of a dictionary of known magnetic resonance fingerprinting (MRF) signal evolutions to determine matches in the NMR signal evolutions to the known MRF signal evolutions or an optimization process. The method also includes generating at least two spatially-resolved measurements indicating quantitative tissue parameters of the subject in at least two locations.

Various embodiments of the present disclosure are directed towards a magnetic resonance imaging (MRI) radio frequency (RF) coil. The MRI RF coil comprises a first conductive ring and a second conductive ring. A plurality of rung groups extend between the first and second conductive rings. The plurality of rung groups are spaced uniformly about the first conductive ring. Each of the plurality of rung groups comprises a plurality of conductive rungs extending between and connected to the first and second conductive rings. The plurality of conductive rungs of each of the plurality of rung groups are azimuthally separated from one another by a first azimuth angle. Each of the plurality of rung groups is separated from a neighboring rung group by a spacing that forms a window. Each of the windows have a second azimuth angle that is greater than the first azimuth angle.

A system for multi-slice magnetic resonance imaging (MM) comprises a gradient coil array comprising a plurality of independent coils distributed about an enclosure; and a controller configured to concurrently actuate said plurality of coils so as to generate a spatially-varying magnetic field within said enclosure such that for at least first and second volumetric slices, a magnetic field magnitude associated with at least one location in the first volumetric slice is substantially equal to a magnetic field magnitude associated with a respective location in the second volumetric slice.

An MR Spectroscopy (MRS) system and approach is provided for measuring spectral information corresponding with propionic acid (PA), either alone or in combination with other measurements corresponding with other chemicals, to diagnose and/or monitor at least one of bacterial infection, such as associated with P. acnes, or conditions related thereto such as nociceptive pain associated with tissue acidity. An interfacing DDD-MRS signal processor receives output signals to produce a post-processed spectrum, with spectral regions corresponding with certain chemicals, including PA, then measured as biomarkers. A diagnostic processor derives a diagnostic value for each disc, and performs certain normalizations, based upon ratios of the spectral regions related to chemicals implicated in degenerative painful tissue pathology, such as PA and hypoxia markers of lactic acid (LA) and alanine (AL), and structural chemicals of proteoglycan (PG) and collagen or carbohydrate (CA).

An MR Spectroscopy (MRS) system and approach is provided for measuring spectral information corresponding with propionic acid (PA), either alone or in combination with other measurements corresponding with other chemicals, to diagnose and/or monitor at least one of bacterial infection, such as associated with P. acnes, or conditions related thereto such as nociceptive pain associated with tissue acidity. An interfacing DDD-MRS signal processor receives output signals to produce a post-processed spectrum, with spectral regions corresponding with certain chemicals, including PA, then measured as biomarkers. A diagnostic processor derives a diagnostic value for each disc, and performs certain normalizations, based upon ratios of the spectral regions related to chemicals implicated in degenerative painful tissue pathology, such as PA and hypoxia markers of lactic acid (LA) and alanine (AL), and structural chemicals of proteoglycan (PG) and collagen or carbohydrate (CA).

An imaging unit of an MRI apparatus performs imaging of a positioning image of a subject including a spine; a first imaging that images a cross section including the spine and extending along a longitudinal direction of the spine; and a second imaging that images a cross section in a direction of traversing the spine. An automatic cross-section position setting unit detects a specific tissue of the spine using a scout image or an image including the spine acquired in the first imaging step, performs a matching process between the detected specific tissue of the spine and a spine model, and calculates an imaging cross-section position of the second imaging based upon a specific tissue position of the spine specified by matching, thereby performing automatic setting.

A method to compensate for chemical shift displacement includes, prior to applying an imaging pulse sequence to acquire MRI data of a subject, applying a first saturation pulse within a slice location of an imaging volume of the subject in which the MRI data is to be acquired, wherein the first saturation pulse results in a first chemical shift displacement between water and fat in a first spatial saturation band. The method also includes, prior to applying the imaging pulse sequence, subsequently applying a second saturation pulse within the slice location, wherein the second saturation pulse results in a second chemical displacement between the water and the fat in a second spatial saturation band that results in a final spatial saturation band being free of chemical shift displacement after application of the second saturation pulse, the second chemical shift displacement being different from the first chemical shift displacement.

An MRI scanner and a method for operation of the MRI scanner are provided. The MRI scanner has a first receiving antenna for receiving a magnetic resonance signal from a patient in a patient tunnel, a second receiving antenna for receiving a signal having the Larmor frequency of the magnetic resonance signal, and a receiver. The second receiving antenna is located outside of the patient tunnel or near an opening thereof. The receiver has a signal connection to the first receiving antenna and the second receiving antenna and is configured to suppress an interference signal by the second receiving antenna in the magnetic resonance signal received by the first receiving antenna.