Accelerating in vivo fast spin echo high angular resolution diffusion imaging with an isotropic resolution in mice through compressed sensing

2020 ◽  
Vol 85 (3) ◽  
pp. 1397-1413
Author(s):  
Maarten Naeyaert ◽  
Jan Aelterman ◽  
Johan Van Audekerke ◽  
Vladimir Golkov ◽  
Daniel Cremers ◽  
...  
Keyword(s):  
Compressed Sensing ◽  
Angular Resolution ◽  
Spin Echo ◽  
Diffusion Imaging ◽  
Fast Spin Echo ◽  
High Angular Resolution ◽  
Isotropic Resolution ◽  
Fast Spin

valuation of the in vivo contrast using fast spin echo MRI sequences between tissues and thermal lesions in rabbit produced by high intensity focused ultrasound

2010 ◽  
Author(s):  
Christakis Damianou ◽  
Kleanthis Ioannides ◽  
Venediktos Hadjisavas ◽  
Nikos Milonas ◽  
Andreas Couppis ◽  
...  
Keyword(s):  
High Intensity ◽  
Focused Ultrasound ◽  
Spin Echo ◽  
High Intensity Focused Ultrasound ◽  
Fast Spin Echo ◽  
Thermal Lesions ◽  
Mri Sequences ◽  
Fast Spin

scholarly journals Knee imaging: Rapid three-dimensional fast spin-echo using compressed sensing

2016 ◽  
Vol 45 (6) ◽  
pp. 1712-1722 ◽  
Author(s):  
Richard Kijowski ◽  
Humberto Rosas ◽  
Alexey Samsonov ◽  
Kevin King ◽  
Rob Peters ◽  
...  
Keyword(s):  
Compressed Sensing ◽  
Spin Echo ◽  
Three Dimensional ◽  
Fast Spin Echo ◽  
Knee Imaging ◽  
Fast Spin

Quantitative in vivo T2 mapping using fast spin echo techniques – A linear correction procedure

NeuroImage ◽  
2017 ◽  
Vol 157 ◽  
pp. 476-485 ◽  
Author(s):  
Ulrike Nöth ◽  
Manoj Shrestha ◽  
Jan-Rüdiger Schüre ◽  
Ralf Deichmann
Keyword(s):  
Spin Echo ◽  
T2 Mapping ◽  
Fast Spin Echo ◽  
Correction Procedure ◽  
Linear Correction ◽  
Fast Spin

scholarly journals In vivo proton electron double resonance imaging of mice With fast spin echo pulse sequence

2011 ◽  
Vol 35 (2) ◽  
pp. 471-475 ◽  
Author(s):  
Ziqi Sun ◽  
Haihong Li ◽  
Sergey Petryakov ◽  
Alex Samouilov ◽  
Jay L. Zweier
Keyword(s):  
Pulse Sequence ◽  
Spin Echo ◽  
Double Resonance ◽  
Fast Spin Echo ◽  
Resonance Imaging ◽  
Echo Pulse ◽  
Fast Spin

Feasibility study of non Carr Purcell Meiboom Gill single shot fast spin echo in spinal cord diffusion imaging

2002 ◽  
Vol 14 (3) ◽  
pp. 243-247 ◽  
Author(s):  
Patrick H. Le Roux ◽  
Anne Darquie ◽  
Pierre G. Carlier ◽  
Chris A. Clark
Keyword(s):  
Spinal Cord ◽  
Feasibility Study ◽  
Spin Echo ◽  
Diffusion Imaging ◽  
Fast Spin Echo ◽  
Single Shot ◽  
Fast Spin

scholarly journals Accelerated whole brain intracranial vessel wall imaging using black blood fast spin echo with compressed sensing (CS-SPACE)

2017 ◽  
Vol 31 (3) ◽  
pp. 457-467 ◽  
Author(s):  
Chengcheng Zhu ◽  
Bing Tian ◽  
Luguang Chen ◽  
Laura Eisenmenger ◽  
Esther Raithel ◽  
...  
Keyword(s):  
Compressed Sensing ◽  
Vessel Wall ◽  
Spin Echo ◽  
Vessel Wall Imaging ◽  
Fast Spin Echo ◽  
Black Blood ◽  
Whole Brain ◽  
Intracranial Vessel ◽  
Fast Spin ◽  
Wall Imaging

scholarly journals In vivo characterization of the connectivity and subcomponents of the human globus pallidus

2015 ◽  
Author(s):  
Patrick Beukema ◽  
Timothy Verstynen ◽  
Fang-Cheng Yeh
Keyword(s):  
Angular Resolution ◽  
Diffusion Imaging ◽  
Orientation Distribution ◽  
High Angular Resolution ◽  
Fiber Direction ◽  
Degree Of Anisotropy ◽  
In Vivo Characterization ◽  
Diffusion Properties

Projections from the substantia nigra and striatum traverse through the pallidum on the way to their targets. To date, in vivo characterization of these pathways remains elusive. Here we used high angular resolution diffusion imaging (N=138) to study the characteristics and structural subcompartments of the human pallidum. Our results show that the diffusion orientation distribution at the pallidum is asymmetrically oriented in a dorsolateral direction, consistent with the orientation of underlying fiber systems. Furthermore, compared to the outer pallidal segment, the internal segment has more peaks in the orientation distribution function and stronger anisotropy in the primary fiber direction, consistent with known cellular differences between the underlying nuclei. These differences in orientation, complexity, and degree of anisotropy are sufficiently robust to automatically segment the pallidal nuclei using diffusion properties. Thus the gray matter diffusion signal can be useful as an in vivo measure of the collective nigrostriatal and striatonigral pathways.

scholarly journals Quality and Stability of Compressed Sensing Schemes in the Fast Spin Echo Sequence

2013 ◽  
Vol 7 ◽  
Author(s):  
Naeyaert Maarten ◽  
Aelterman Jan ◽  
Van Audekerke Johan ◽  
Verhoye Marleen
Keyword(s):  
Compressed Sensing ◽  
Spin Echo ◽  
Fast Spin Echo ◽  
Spin Echo Sequence ◽  
Fast Spin Echo Sequence ◽  
Fast Spin

scholarly journals Evaluation of the contrast between tissues and thermal lesions in rabbit in vivo produced by high intensity focused ultrasound using fast spin echo MRI sequences

2011 ◽  
Vol 04 (01) ◽  
pp. 51-61 ◽  
Author(s):  
Venediktos Hadjisavvas ◽  
Kleanthis Ioannides ◽  
Michalis Komodromos ◽  
Nikos Mylonas ◽  
Christakis Damianou
Keyword(s):  
High Intensity ◽  
Focused Ultrasound ◽  
Spin Echo ◽  
High Intensity Focused Ultrasound ◽  
Fast Spin Echo ◽  
Thermal Lesions ◽  
Mri Sequences ◽  
Fast Spin
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