scholarly journals Fast T2 mapping with multiple echo, caesar cipher acquisition and model-based reconstruction

2014 ◽  
Vol 73 (3) ◽  
pp. 1065-1074 ◽  
Author(s):  
Christopher L. Lankford ◽  
Richard D. Dortch ◽  
Mark D. Does
Keyword(s):  
2011 ◽  
Vol 34 (2) ◽  
pp. 420-428 ◽  
Author(s):  
Tilman J. Sumpf ◽  
Martin Uecker ◽  
Susann Boretius ◽  
Jens Frahm

2018 ◽  
Vol 48 (2) ◽  
pp. 359-368 ◽  
Author(s):  
Tom Hilbert ◽  
Tilman J. Sumpf ◽  
Elisabeth Weiland ◽  
Jens Frahm ◽  
Jean-Philippe Thiran ◽  
...  
Keyword(s):  

2014 ◽  
Vol 33 (12) ◽  
pp. 2213-2222 ◽  
Author(s):  
Tilman J. Sumpf ◽  
Andreas Petrovic ◽  
Martin Uecker ◽  
Florian Knoll ◽  
Jens Frahm

PLoS ONE ◽  
2021 ◽  
Vol 16 (9) ◽  
pp. e0252777
Author(s):  
Dan Zhu ◽  
Haiyan Ding ◽  
M. Muz Zviman ◽  
Henry Halperin ◽  
Michael Schär ◽  
...  

Purpose We aim to determine an advantageous approach for the acceleration of high spatial resolution 3D cardiac T2 relaxometry data by comparing the performance of different undersampling patterns and reconstruction methods over a range of acceleration rates. Methods Multi-volume 3D high-resolution cardiac images were acquired fully and undersampled retrospectively using 1) optimal CAIPIRINHA and 2) a variable density random (VDR) sampling. Data were reconstructed using 1) multi-volume sensitivity encoding (SENSE), 2) joint-sparsity SENSE and 3) model-based SENSE. Four metrics were calculated on 3 naïve swine and 8 normal human subjects over a whole left-ventricular region of interest: root-mean-square error (RMSE) of image signal intensity, RMSE of T2, the bias of mean T2, and standard deviation (SD) of T2. Fully sampled data and volume-by-volume SENSE with standard equally spaced undersampling were used as references. The Jaccard index calculated from one swine with acute myocardial infarction (MI) was used to demonstrate preservation of segmentation of edematous tissues with elevated T2. Results In naïve swine and normal human subjects, all methods had similar performance when the net reduction factor (Rnet) <2.5. VDR sampling with model-based SENSE showed the lowest RMSEs (10.5%-14.2%) and SDs (+1.7–2.4 ms) of T2 when Rnet>2.5, while VDR sampling with the joint-sparsity SENSE had the lowest bias of mean T2 (0.0–1.1ms) when Rnet>3. The RMSEs of parametric T2 values (9.2%-24.6%) were larger than for image signal intensities (5.2%-18.4%). In the swine with MI, VDR sampling with either joint-sparsity or model-based SENSE showed consistently higher Jaccard index for all Rnet (0.71–0.50) than volume-by-volume SENSE (0.68–0.30). Conclusions Retrospective exploration of undersampling and reconstruction in 3D whole-heart T2 parametric mapping revealed that maps were more sensitive to undersampling than images, presenting a more stringent limiting factor on Rnet. The combination of VDR sampling patterns with model-based or joint-sparsity SENSE reconstructions were more robust for Rnet>3.


2014 ◽  
Vol 36 (11) ◽  
pp. 1428-1435 ◽  
Author(s):  
Xi Peng ◽  
Xin Liu ◽  
Hairong Zheng ◽  
Dong Liang

2020 ◽  
Vol 43 ◽  
Author(s):  
Peter Dayan

Abstract Bayesian decision theory provides a simple formal elucidation of some of the ways that representation and representational abstraction are involved with, and exploit, both prediction and its rather distant cousin, predictive coding. Both model-free and model-based methods are involved.


2001 ◽  
Vol 7 (S2) ◽  
pp. 578-579
Author(s):  
David W. Knowles ◽  
Sophie A. Lelièvre ◽  
Carlos Ortiz de Solόrzano ◽  
Stephen J. Lockett ◽  
Mina J. Bissell ◽  
...  

The extracellular matrix (ECM) plays a critical role in directing cell behaviour and morphogenesis by regulating gene expression and nuclear organization. Using non-malignant (S1) human mammary epithelial cells (HMECs), it was previously shown that ECM-induced morphogenesis is accompanied by the redistribution of nuclear mitotic apparatus (NuMA) protein from a diffuse pattern in proliferating cells, to a multi-focal pattern as HMECs growth arrested and completed morphogenesis . A process taking 10 to 14 days.To further investigate the link between NuMA distribution and the growth stage of HMECs, we have investigated the distribution of NuMA in non-malignant S1 cells and their malignant, T4, counter-part using a novel model-based image analysis technique. This technique, based on a multi-scale Gaussian blur analysis (Figure 1), quantifies the size of punctate features in an image. Cells were cultured in the presence and absence of a reconstituted basement membrane (rBM) and imaged in 3D using confocal microscopy, for fluorescently labeled monoclonal antibodies to NuMA (fαNuMA) and fluorescently labeled total DNA.


Author(s):  
Charles Bouveyron ◽  
Gilles Celeux ◽  
T. Brendan Murphy ◽  
Adrian E. Raftery

Author(s):  
Jonathan Jacky ◽  
Margus Veanes ◽  
Colin Campbell ◽  
Wolfram Schulte
Keyword(s):  

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