Abstract: A pulse sequence generation computing device for a magnetic resonance imaging (MRI) system includes a processor in communication with a memory device. The processor is programmed to receive a pulse sequence including a plurality of gradient pulses and provide a pulse sequence threshold function corresponding to an acoustic noise reduction level. For each gradient pulse in the pulse sequence, the processor is programmed to determine an amplitude and a slew rate of the gradient pulse, determine a threshold amplitude and slew rate of the gradient pulse, and compare the determined amplitude and slew rate to the threshold amplitude and slew rate. If either the determined amplitude or slew rate exceeds the threshold amplitude or slew rate, the processor adjusts at least one of the amplitude and the slew rate of the gradient pulse to an amplitude and a slew rate as defined by the pulse sequence threshold function.

Abstract: The present disclosure describes non-invasive approaches for delineating and characterizing tissue using MR imaging over a range of treatment levels. By way of example, tumor tissue may be distinguished and delineated from other tissue, such as muscle tissue. Further, tumor tissue may be characterized as malignant or benign using such approaches.

Abstract: A system and method for tracking temperature changes in tissue and bone is disclosed. In one aspect, the temperature changes are tracked simultaneously with high spatial encoding and temporal efficiency. The method is robust in terms of B0 and chemical shift off-resonance, as well as insensitive to eddy currents for accurate temperature mapping. Zero TE (ZTE) based MR thermometry is utilized herein to extract temperature changes from proton density and T1 weighted images. Additionally, T1 signal contamination is corrected for by calibrating T1 and B0 by using a variable flip angle method to achieve temperature mapping in bone, aqueous and adipose tissue simultaneously.

Abstract: A system and method for tracking temperature changes in tissue and bone is disclosed. In one aspect, the temperature changes are tracked simultaneously with high spatial encoding and temporal efficiency. The method is robust in terms of B0 and chemical shift off-resonance, as well as insensitive to eddy currents for accurate temperature mapping. Zero TE (ZTE) based MR thermometry is utilized herein to extract temperature changes from proton density and T1 weighted images. Additionally, T1 signal contamination is corrected for by calibrating T1 and B0 by using a variable flip angle method to achieve temperature mapping in bone, aqueous and adipose tissue simultaneously.

Abstract: The present disclosure describes non-invasive approaches for delineating and characterizing tissue using MR imaging over a range of treatment levels. By way of example, tumor tissue may be distinguished and delineated from other tissue, such as muscle tissue. Further, tumor tissue may be characterized as malignant or benign using such approaches.