In a method and magnetic resonance apparatus for recording diagnostic measurement data of a heart of an examination object, the magnetic resonance apparatus is operated by a control sequence wherein an RF pulse excites nuclear spins with a flip angle of at least 60, the diagnostic measurement data are recorded in a coordinate system independent of the heart, and the basic magnetic field produced by the magnetic resonance apparatus is smaller than 1.0 tesla.

The present invention relates generally to medical imaging and, more particularly, relates to systems and methods for obtaining magnetic resonance (MR) images of tissues and organs (particularly of the heart) or parts thereof.

In a method and apparatus for magnetic resonance imaging preview and establishing an MR model, an MRI scanner is controlled so as to execute an MR model scan sequence to perform an MRI scan of a designated patient, to obtain an MR model of the patient. One type of scan sequence is sequentially selected from all types of scan sequence supported by the MRI device, and one parameter set is sequentially selected from at least one parameter set supported by this type of scan sequence. The selected sequence and the selected parameter set are used to subject the MR model to a virtual MRI scan, to obtain an MR preview image corresponding to the selected sequence and the selected parameter set for the sequence C. This is repeated for all types of scan sequence supported by the MRI scanner and all parameter sets supported by each type of scan sequence. An MR model of a patient can thereby be established, and MR images of the patient to be previewed quickly, before an MRI scan of the patient is actually begun.

A magnetic resonance fingerprinting (MRF) method for determining parameter values in pixels of an examination object can use a magnetic resonance system with, for example, a constant magnetic field strength (e.g. of less than 1.5 tesla or a constant magnetic field strength of less than 0.5 tesla). The MRF method can be adapted for conditions that prevail with such low-field magnetic resonance systems, thus enabling the parameter values to be advantageously determined efficiently while simultaneously maintaining a high degree of quality.

A magnetic resonance imaging apparatus according to an embodiment includes a collection unit and a generation unit. The collection unit collects data of an imaging area over a plurality of time phases within a certain respiratory cycle after applying a labeling pulse to a labeling area in which cerebrospinal fluid flows under a task of respiration. The generation unit generates images of a plurality of time phases depicting the cerebrospinal fluid by using the collected data.

Provided is a system and method for performing a magnetic resonance fingerprinting imaging process. The process includes determining acquisition parameters including at least one of repetition time (TR) or flip angle (FA), selected to control one of a duration and a number of repetitions of for a pulse sequence that samples k-space in a Cartesian acquisition pattern by acquiring an echo train. The process also includes controlling a magnetic resonance imaging (MRI) system to perform the pulse sequence a plurality of times to acquire magnetic resonance fingerprinting (MRF) data corresponding to signals from the subject excited by the pulse sequence. The process also includes estimating quantitative tissue properties of the subject by comparing the MRF data to a database and reconstructing, from the MRF data, at least one image of the subject indicating the estimated quantitative tissue properties.

A low-field magnetic resonance imaging (MRI) system. The system includes a plurality of magnetics components comprising at least one first magnetics component configured to produce a low-field main magnetic field B.sub.0 and at least one second magnetics component configured to acquire magnetic resonance data when operated, and at least one controller configured to operate one or more of the plurality of magnetics components in accordance with at least one low-field zero echo time (LF-ZTE) pulse sequence.

A retrospective reconstruction method uses cardiac self-gating for patients with severe arrhythmias. Self-gated myocardial systolic and diastolic motion is determined from low-spatial and high-temporal resolution images and then the MRI-dataset is retrospectively reconstructed to obtain high quality images. The method uses undersampled image reconstruction to obtain the low-spatial and high-temporal resolution images, including those of different beat morphologies. Processing of these images is utilized to generate a cardiac phase signal. This signal allows for arrhythmia detection and cardiac phase sorting. The cardiac phase signal allows for detection of end-systolic and diastolic events which allows for improved sampling efficiency. In the case of frequent and severe arrhythmia, the method utilizes data from the normal and interrupted beats to improve sampling and image quality.

The present invention relate to a system and associate method of MRI and MR spectroscopy which provide stable measurements of the relaxation times, T1 and T2, by using tailored multi-band RF pulses that direct control of the saturation conditions in the background pool of macro-molecular protons, and hence provide a flexible means to induce constant Magnetisation Transfer (MT) effects. In doing this, equal saturation of the background pool is obtained for all measurements independent of the parameters that may be changed, for example, the rotation rate used to obtain a desired flip angle, that is, the degree of change in the magnetisation of the free pool of protons.

A system and method is provided for performing a magnetic resonance fingerprinting (MRF) study in the face of inhomogeneous magnetic fields. The process includes performing a balanced steady-state free precession (bSSFP) pulse sequence multiple times to acquire a multiple MRF datasets from at region of interest (ROI) in a subject, wherein performing the multiple bSSFP pulse sequences includes cycling through multiple phase patterns that differ across the multiple times. The process also includes comparing the multiple MRF datasets with a MRF dictionary to determine at least one tissue property indicated by each of the multiple MRF datasets, producing an aggregated indication of the at least one tissue property, and producing at least one map of the at least one tissue property using the aggregated indication of the at least one tissue property.