An IR pulse is applied to a tag region B that is disposed at the upstream side of the ascending aorta relative to a tag region A at a timing with a second predetermined delay time TD2 (for example, 600 ms) from the application time of an IR pulse to the tag region A to thereby perform tagging. By this tagging, it is possible to suppress the MR signals derived from the substantial portions and the blood within the tag region B. Subsequently, an imaging scan is performed after a predetermined time lapse TIA (for example, 1200 ms) from the application time of the IR pulse to the tag region A or after a predetermined time lapse TIB (for example, 600 ms) from the application time of the IR pulse to the tag region B.

The present disclosure is directed to combined angiography and perfusion using radial imaging and arterial spin labeling.

Described here are systems and methods for generating quantitative perfusion parameter maps based on different longitudinal relaxation parameter maps that are produced from images acquired using non-selective and selective magnetic resonance imaging (“MRI”) data acquisition techniques.

A magnetic resonance imaging apparatus according to an embodiment includes an execution unit and a generation unit. The execution unit executes first data collection after a predetermined inversion time elapses from a time when a labeling pulse is applied to a fluid flowing into an imaging region of a subject and a second data collection without application of the labeling pulse. The generation unit generates a differential image by using the first data and the second data. Here, the generation unit generates the differential image by a different differential method according to a relationship between the inversion time and a longitudinal relaxation time of the fluid.

A magnetic resonance imaging (MRI) system, method and/or computer readable medium is configured to effect magnetic resonance angiography (MRA) images with reduced motion artifacts includes acquiring a plurality of k-space data sets by traversing a plurality of radial trajectories in three-dimensional (3D) k-space, generating a plurality of 3D MR images derived from k-space populated by the k-space data sets, aligning the 3D MR images with respect to each other, determining one or more motion parameters for the object based upon the aligning, modifying values of k-space data sets using the determined one or more motion parameters, generating a motion-corrected 3D MR image from a combination of acquired k-space data sets including the modified values.

The present invention is directed to a system and method for measuring blood volume using non-contrast-enhanced magnetic resonance imaging. The method of the present invention includes a subtraction-based method using a pair of acquisitions immediately following velocity-sensitized pulse trains for the label module and its corresponding control module, respectively. The signal of static tissue is canceled out and the difference signal comes from the flowing blood compartment above a cutoff velocity. After normalizing to a proton density-weighted image acquired separately and scaled with the blood T1 and T2 relaxation factors, quantitative measurement of blood volume is then obtained.

Systems and methods for reducing acoustic noise in a Magnetic Resonance Imaging (MRI) are provided. One method includes applying a labeling phase of an arterial spin labeling (ASL) pulse sequence to a region of interest, applying a three-dimensional (3D) radial pulse sequence to the region of interest to generate a tag image, applying a control phase of the ASL pulse sequence to the region of interest, and applying the 3D radial pulse sequence to the region of interest to generate a control image.

Described herein is a method to detect perfusion and brain functional activity using Hyperpolarized xenon-129 (.sup.129Xe) Time-of-Flight (TOF) Magnetic Resonance Imaging (MRI). Specifically, this method uses hyperpolarized .sup.129Xe MRI to detect blood flow and perfusion changes in the region of interest. In addition, this method can be used to detect blood flow changes in brain tissue that corresponds to the brain functional activities by detecting the amount of .sup.129Xe dissolved in blood and brain tissue per unit of time.

A method of operating a magnetic resonance imaging system (10) with regard to acquiring multiple-phase dynamic contrast-enhanced magnetic resonance images, the method comprising steps of acquiring (48) a first set of magnetic resonance image data (x.sub.pre) prior to administering a contrast agent to the subject of interest (20), by employing a water/fat magnetic resonance signal separation technique, determining (52) a first image of the spatial distribution of fat (I.sub.pre) of at least the portion of the subject of interest (20), acquiring (50) at least a second set of magnetic resonance image data (x.sub.2) of at least the portion of the subject of interest (20) after administering the contrast agent to the subject of interest (20), by employing a water/fat magnetic resonance signal separation technique, determining (54) at least a second image of the spatial distribution of fat (I.sub.2.sup.ph) of at least the portion of the subject of interest (20), applying (56) an image registration method to the second image of the spatial distribution of fat (I.sub.2.sup.ph) with reference to the first image of the spatial distribution of fat (I.sub.pre) for correcting a potential motion of the subject of interest (20); and a magnetic resonance imaging system (10) having a control unit (26) that is configured to carry out steps (56-64) of such a method; and a software module (44) for carrying out such a method, wherein the method steps (56-64) to be conducted are converted into a program code that is implementable in a memory unit (30) and is executable by a processor unit (32) of the magnetic resonance imaging system (10).

A magnetic resonance system (10), and corresponding method, image a subject using a conversion-free interleaved black and bright blood imaging (cfIBBI) sequence. A MR scanner (12) is controlled to perform a plurality of repetitions of a black blood imaging sequence (52). The black blood imaging sequence (52) includes a tissue nulling sub-sequence followed by a black blood acquisition sub-sequence (56) performed a time interval (TI) after the tissue nulling sub-sequence. The MR scanner (12) is further controlled to, between successive repetitions of the black blood imaging sequence (52), perform a bright blood imaging sequence (54) including the tissue nulling sub-sequence followed by a bright blood acquisition sub-sequence (58) performed the time interval (TI) after the tissue nulling sub-sequence. The time intervals (TI) of the black blood imaging sequence (52) and the bright blood imaging sequence (54) are of the same duration.