In a method and magnetic resonance (MR) apparatus for pulse wave velocity (PWV) measurement along the aorta of a subject using MR imaging, a multislice cardio synchronized segmented ciné MR data acquisition sequence is optimized in order to enhance inflow representation in the slice images, in order to make the multislice MR data acquisition sequence viable for clinical uses, so as to acquire intensity-based MR data from two transverse slices spaced from each other along the descending aorta. The respective intensities of relevant pixels in at least two respective slice images are analyzed in order to identify the arrival of a pulse wave in the respective slices by the onset of flow enhancement in the slices, represented by intensity changes in the pixels. From the onset of flow enhancement in the respective slice images, PWV is calculated. An electronic signal representing the calculated PWV is then provided from a computer.

A method for adapting, per cardiac cycle, the parameters governing interpolation of varying and non-interpolation of fixed fractions of each individual cardiac cycle is provided. A time series of data values associated with a cardiac cycle is received, and the time series is scaled to a reference cardiac cycle, wherein the scaling includes applying a model to the time series to generate a scaled time series of data values associated with the first cardiac cycle. The model is trained using the scaled time series.

The present disclosure may provide imaging methods, systems and storage media. The imaging methods may include: obtaining first imaging data acquired by an imaging device, wherein the first imaging data includes data corresponding to a plurality of cardiac cycles; and performing image reconstruction on data corresponding to the plurality of cardiac cycles in the first imaging data to acquire one or more cardiac cines. Each cardiac cine of the one or more cardiac cines may include cardiac images of a plurality of phases in at least one cardiac cycle.

Systems and methods for generating MRI images of the lungs and/or airways of a subject using a medical grade gas mixture comprises between about 20-79% inert perfluorinated gas and oxygen gas. The images are generated using acquired .sup.19F magnetic resonance image (MRI) signal data associated with the perfluorinated gas and oxygen mixture.

One aspect of the present subject matter provides an imaging method including: receiving a trigger signal; after a period substantially equal to a trigger delay minus an inversion delay, applying a non-selective inversion radiofrequency pulse to a region of interest followed by a slice-selective reinversion radiofrequency pulse to a slice of the region of interest of a subject; and after lapse of the trigger delay commenced at the cardiac cycle signal, acquiring a plurality of time-resolved images of the slice of the region of interest from an imaging device.

Systems and methods for joint reconstruction and segmentation of organs from magnetic resonance imaging (MRI) data are provided. Sparse MRI data is received at a computer system, which jointly processes the MRI data using a plurality of reconstruction and segmentation processes. The MRI data is processed using a joint reconstruction and segmentation process to identify an organ from the MRI data. Additionally, the MRI data is processed using a channel-wise attention network to perform static reconstruction of the organ from the MRI data. Further, the MRI data can is processed using a motion-guided network to perform dynamic reconstruction of the organ from the MRI data. The joint processing allows for rapid static and dynamic reconstruction and segmentation of organs from sparse MRI data, with particular advantage in clinical settings.

Reference data relating to a portion of a patient anatomy during patient motion can be acquired from a magnetic resonance imaging system (MRI) to develop a patient motion library. During a time of interest, tracking data is acquired that can be related to the reference data. Partial volumetric data is acquired during the time of interest and at approximately the same time as the acquisition of the tracking data. A volumetric image of patient anatomy that represents a particular motion state can be constructed from the acquired partial volumetric data and acquired tracking data.

Improved magnetic resonance imaging systems, methods and software are described including a low field strength main magnet, a gradient coil assembly, an RF coil system, and a control system configured for the acquisition and processing of magnetic resonance imaging data from a patient while utilizing a sparse sampling imaging technique.

Apparatus and techniques are described herein for nuclear magnetic resonance (MR) projection imaging. Such projection imaging may be used to control radiation therapy delivery to a subject, such as including receiving reference imaging information, generating a two-dimensional (2D) projection image using imaging information obtained via nuclear magnetic resonance (MR) imaging, the 2D projection image corresponding to a specified projection direction, the specified projection direction including a path traversing at least a portion of an imaging subject, determining a change between the generated 2D projection image and the reference imaging information, and controlling delivery of the radiation therapy at least in part using the determined change between the obtained 2D projection image and the reference imaging information.

Provided herein are systems and methods for generating fetal cardiac magnetic resonance (MR) images of a living fetus, within a uterus of a parent of the fetus, by imaging the fetus within the uterus using a magnetic resonance imaging (MRI) system. Also provided herein are methods for deriving information indicative of fetal cardiac cycles from MR data obtained by an MRI system while imaging the fetus, the MR data including MR data for the center of k-space. The derived information may be used to differentiate the fetal cardiac cycles from other sources of noise in the MR data such as the parental cardiac cycles.