A system and method for simultaneous multi-slice nuclear spin tomography is provided which requires no sensitivity profile of a receiving coil along a slice axis. A pulse space region to be sampled can be specified. A first pulse space dimension (k.sub.y) can be assigned to a first phase-encoded axis and a second pulse space dimension (k.sub.z) can be assigned to a second phase-encoded axis and the second phase-encoded axis corresponds to the slice axis. A sampling scheme can also be specified, and a complete sampled can be provided along the second pulse space dimension (k.sub.z). A magnetic resonance scan can then be carried out within the pulse space region to be sampled based on the sampling scheme and respective phase-encodings of the first and second phase-encoded axis.

In order to remove restriction on the number of additions in imaging for offsetting errors caused by hardware performance and/or signal fluctuation caused by a hardware control method by inverting the polarity of predetermined hardware output, the present invention executes a first imaging sequence and a second imaging sequence in which the polarity of a predetermined gradient magnetic field pulse in the first imaging sequence was inverted, adds data acquired in each imaging sequence, and then acquires addition images. In order to perform the addition, each coefficient is determined so that the total of coefficients by which first data acquired in the first imaging sequence are to be multiplied is equal to the total of coefficients by which second data acquired in the second imaging sequence are to be multiplied.

The present invention provides a magnetic resonance imaging system for imaging a subject by a multi-shot imaging. The magnetic resonance imaging system comprises an acquiring unit for acquiring MR raw data corresponding to a plurality of shots; an imaging unit for generating a plurality of folded images from the MR raw data, wherein each of the plurality of folded images is generated from a subset of the MR raw data; a deriving unit for deriving magnitude of each pixel of each folded image; a detecting unit for detecting a motion of the subject during the multi-shot imaging based on similarity measurements of any two folded images of the plurality of folded images, wherein the detecting unit further comprises a first deriving unit configured to derive the measured similarities; and a reconstructing unit for reconstructing a MR image of the subject based on MR raw data obtained according to a detection result of the detecting unit. Since the partially acquired MR raw data is used for motion detection directly, it would be more rapid and stable.

The disclosure relates to magnetic resonance imaging triggered by a prospective acquisition correction sequence. The technique comprises determining repetition time and an acquisition window time of a single-shot fast spin echo sequence; determining the maximum imaging layer number N in each physiological movement cycle on the basis of the acquisition window time and the repetition time, where N is a positive integer greater than or equal to 2; and enabling the single-shot fast spin echo sequence to obtain M layers of imaging data within at least one acquisition window time when the prospective acquisition correction sequence generates a trigger signal, where M is a positive integer greater than or equal to 2 and less than or equal to N. According to the present disclosure, a plurality of layers of imaging data are obtained within a single acquisition window time, thereby increasing a scanning speed and shortening imaging time.

An image processing apparatus according to an embodiment includes processing circuitry. The processing circuitry is configured to generate, from three-dimensional medical image data, a first cross-sectional image and a second cross-sectional image intersecting the first cross-sectional image and is configured to change display locations of the first cross-sectional image and the second cross-sectional image on a display, in conjunction with a change in an intersecting location of the first and the second cross-sectional images.

The present invention provides a magnetic resonance imaging system for imaging a subject by a multi-shot imaging. The magnetic resonance imaging system comprises an acquiring unit for acquiring MR raw data corresponding to a plurality of shots; an imaging unit for generating a plurality of folded images from the MR raw data, wherein each of the plurality of folded images is generated from a subset of the MR raw data; a deriving unit for deriving magnitude of each pixel of each folded image; a detecting unit for detecting a motion of the subject during the multi-shot imaging based on similarity measurements of any two folded images of the plurality of folded images, wherein the detecting unit further comprises a first deriving unit configured to derive the measured similarities; and a reconstructing unit for reconstructing a MR image of the subject based on MR raw data obtained according to a detection result of the detecting unit. Since the partially acquired MR raw data is used for motion detection directly, it would be more rapid and stable.

The present invention describes a method for magnetic resonance (MR) and/or MR imaging, comprising acquisition of signals and MR images originating from a RF and gradient sequence causing isotropic diffusion weighting of signal attenuation, wherein the isotropic diffusion weighting is achieved by one time-dependent dephasing vector q(t) having an orientation, wherein the isotropic diffusion weighting is proportional to the trace of a diffusion tensor D, and wherein the orientation of the time-dependent dephasing vector q(t) is either varied discretely in more than three directions in total, or changed continuously, or changed in a combination of discretely and continuously during the gradient pulse sequence, 0≦t≦echo time, where t represents the time. The method may be performed during a single shot (single MR excitation).

In a method and magnetic resonance (MR) system to acquire MR data in a predetermined volume segment of an examination subject, the data are acquired with at least one echo train that includes at least two signal echoes. The same number of echoes is acquired for each echo train of the at least one echo train, with this number of echoes corresponding to an echo train length. The total number of echoes that are required to acquire the MR data and the echo train length is adapted so that the total number corresponds to a whole number multiple of the echo train length.

The invention relates to a method of MR imaging of an object (10) placed in an examination volume of a MR device (1). It is an object of the invention to enable MR signal acquisition in a single scan providing the necessary information for electric properties imaging (EPT), namely a phase map as well as tissue boundaries. The method of the invention comprises the following steps: —subjecting the object (10) to a multi echo steady state imaging sequence or a fast spectroscopic imaging sequence comprising RF pulses and switched magnetic field gradients, wherein two or more echo signals are generated after each RF excitation; —acquiring the echo signals; —deriving a magnitude image and a phase map from the acquired echo signals, which phase map represents the spatial RF field distribution induced by the RF pulses in the object (10); and —reconstructing an electric conductivity map from the magnitude image and from the phase map, wherein tissue boundaries are derived from at least the magnitude image. Moreover, the invention relates to a MR device for carrying out this method as well as to a computer program to be run on a MR device.

The invention provides a method of medical imaging. The method comprises: receiving, for a current active time window (204A-N) and during a brain activity analysis session (200, 500), fMRI data of a region of interest (309) of a subject (318) in an active state. A transverse relaxation, T2*, map may be generated from the fMRI data using a predefined model of fMRI data variations. The generated T2* map may be compared with a reference T2* map. A blood-oxygen-level dependent (BOLD) response of the region of interest (309) during the current active time window (204 A-N) may be estimated using the results of the comparison.