Accelerated multicontrast volumetric imaging with isotropic resolution for improved peri-infarct characterization using parallel imaging, low-rank and spatially varying edge-preserving sparse modeling

2017 ◽  
Vol 79 (6) ◽  
pp. 3018-3031 ◽  
Author(s):  
Li Zhang ◽  
Peng Lai ◽  
Mihaela Pop ◽  
Graham A. Wright
2013 ◽  
Vol 60 (11) ◽  
pp. 3083-3092 ◽  
Author(s):  
Anthony G. Christodoulou ◽  
Haosen Zhang ◽  
Bo Zhao ◽  
T. Kevin Hitchens ◽  
Chien Ho ◽  
...  

2006 ◽  
Vol 57 (1) ◽  
pp. 8-21 ◽  
Author(s):  
Ashish Raj ◽  
Gurmeet Singh ◽  
Ramin Zabih ◽  
Bryan Kressler ◽  
Yi Wang ◽  
...  

2020 ◽  
Author(s):  
Antoine Klauser ◽  
Paul Klauser ◽  
Frédéric Grouiller ◽  
Sebastien Courvoisier ◽  
Francois Lazeyras

There is a growing interest of the neuroscience community to map the distribution of brain metabolites in vivo. Magnetic resonance spectroscopy imaging (MRSI) is often limited by either a poor spatial resolution and/or a long acquisition time which severely limits its applications for clinical or research purposes. We developed a novel acquisition-reconstruction technique combining fast 1H-FID-MRSI sequence accelerated by random k-space undersampling and a low-rank and total-generalized variation (TGV) constrained model. This framework was applied to the brain of four healthy volunteers. Following 20 min acquisition, reconstruction and quantification, the resulting metabolic maps with a 5 mm isotropic resolution reflected the detailed neurochemical composition of all brain regions and revealed part of the underlying brain anatomy. Contrasts and features from the 3D metabolite distributions were in agreement with the literature and consistent across the four subjects. The successful combination of the 3D 1H-FID-MRSI with a constrained reconstruction enables the detailed mapping of metabolite concentrations at high-resolution in the whole brain and with an acquisition time that is compatible with clinical or research settings.


2021 ◽  
Author(s):  
Xi Chen ◽  
Wenchuan Wu ◽  
Mark Chiew

Three-dimensional (3D) encoding methods are increasingly being explored as alternatives to multi-slice two-dimensional (2D) acquisitions in fMRI, particularly in cases where high isotropic resolution is needed. 3D multi-shot EPI is the most popular 3D fMRI acquisition method, but is susceptible to physiological fluctuations which can induce inter-shot phase variations, and thus reducing the achievable tSNR, negating some of the benefit of 3D encoding. This issue can be particularly problematic at ultra-high fields like 7T, which have more severe off-resonance effects. In this work, we aim to improve the temporal stability of 3D multi-shot EPI at 7T by improving its robustness to inter-shot phase variations. We presented a 3D segmented CAIPI sampling trajectory ("seg-CAIPI") and an improved reconstruction method based on Hankel structured low-rank matrix recovery. Simulation and in-vivo results demonstrate that the combination of the seg-CAIPI sampling scheme and the proposed structured low-rank reconstruction is a promising way to effectively reduce the unwanted temporal variance induced by inter-shot physiological fluctuations, and thus improve the robustness of 3D multi-shot EPI for fMRI.


2015 ◽  
Vol 75 (4) ◽  
pp. 1499-1514 ◽  
Author(s):  
Justin P. Haldar ◽  
Jingwei Zhuo

2020 ◽  
Vol 85 (3) ◽  
pp. 1455-1467
Author(s):  
Ziyu Meng ◽  
Rong Guo ◽  
Yudu Li ◽  
Yue Guan ◽  
Tianyao Wang ◽  
...  

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