ELECTRONIC POSTER - ismrm
ELECTRONIC POSTER - ismrm
ELECTRONIC POSTER - ismrm
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Thursday 13:30-15:30 Computer 56<br />
13:30 4005. Evidence for Microscopic Diffusion Anisotropy in Spinal Cord Tissue Observed<br />
with DWV Imaging on a Whole-Body MR System<br />
Marco Lawrenz 1 , Martin Koch 1 , Jürgen Finsterbusch 1<br />
1 Department of Systems Neuroscience, University Medical Center, Hamburg-Eppendorf, Hamburg, Germany<br />
Double-wave-vector diffusion-weighted imaging is able to detect microscopic diffusion anisotropy in macroscopically isotropic<br />
samples. So far, corresponding experiments were performed on NMR systems with high performance gradient coils (>=300mT/m).<br />
Here, experiments are presented that provide evidence for the observation of the anisotropy effect on a standard whole-body MR<br />
system.<br />
14:00 4006. Numerical Simulations of Double-Wave-Vector Diffusion-Weighting Experiments<br />
with Multiple Concatenations at Short Mixing Times<br />
Jürgen Finsterbusch 1,2<br />
1 Department of Systems Neuroscience , University Medical Center Hamburg-Eppendorf, Hamburg, Germany;<br />
2 Neuroimage Nord, University Medical Centers Hamburg-Kiel-Lübeck, Hamburg-Kiel-Lübeck, Germany<br />
Double-wave-vector diffusion-weighting experiments where two diffusion weighting periods are applied successively in a single<br />
acquisition are a promising tool to investigate tissue microstructure, e.g. cell or compartment sizes. However, for the long gradient<br />
pulse durations required on whole-body MR systems the underlying signal modulation with the angle between the two wave vectors<br />
may be small which hampers the detectability of the effect. Here, it is shown that multiple concatenations of the two diffusion<br />
weightings in a single experiment can yield considerably higher signal modulations than expected theoretically because shorter<br />
gradient pulses are sufficient to achieve the desired diffusion weighting.<br />
14:30 4007. Multiple Echo Multi Shot (MEMS) Diffusion Sequence<br />
Sergio Uribe 1,2 , César Galindo 3 , Cristian Tejos, 2,4 , Pablo Irarrazaval, 2,4 , Steren<br />
Chabert 3<br />
1 Radiology Department, Pontificia Universidad Catolica de Chile, Santiago, Chile; 2 Biomedical Imaging<br />
Center, Pontificia Universidad Catolica de Chile, Santiago, Chile; 3 Biomedical Engineering Department,<br />
Universidad de Valparaiso, Valparaiso, Chile; 4 Electrical Engineering Department, Pontificia Universidad<br />
Catolica de Chile, Santiago, Chile<br />
T2 and diffusion measurements are usually acquire in different scans. In this work we propose a multi echo multi shot diffusion<br />
sequence that allows us obtaining T2 and mean diffusivity from a single scan. The multi shot approach enable short echo times for<br />
both echoes. This characteristic makes this sequence suitable to be applied in tissues with short T2. Result of in vivo experiments<br />
show an excellent correlation of T2 and mean diffusivity of the muscle compare to standard scans.<br />
15:00 4008. Extension of the Double Wave Vector Experiments at Long Mixing Times to<br />
Multiple Concatenations<br />
Marco Lawrenz 1 , Jürgen Finsterbusch 1<br />
1 Department of Systems Neuroscience, University Medical Center, Hamburg-Eppendorf, Hamburg, Germany<br />
An extension of the tensor approach to the double wave-vector experiment for multiple concatenations is presented aiming at the<br />
examination of microscopic anisotropy in tissue for fully restricted diffusion. A detailed analysis of the generalized tensor expression<br />
to the fourth order does not only hold for the characterization of arbitrary pores in an idealized environment but can still derive a<br />
microscopic anisotropy measure on the pore size level with sufficient accuracy for timing parameters compatible to whole-body MR<br />
systems. Monte Carlo simulations confirm the theoretical considerations.<br />
Tractography<br />
Hall B Monday 14:00-16:00 Computer 57<br />
14:00 4009. Fast Normalization of Probabilistic Tractography<br />
Stephen Edward Jones 1,2 , Kenneth Sakaie<br />
1 Neuroradiology, Cleveland Clinic, Cleveland, OH, United States<br />
Numerical computation of track density using probabalistic DWI can be inefficient, particularly for distant points. We present a<br />
method that uses a partial differential equation approach (Laplace's equation) to solve the special isotropic case of probablistic<br />
tracking. This provides a rapid solution for any two points within the brain, with arbitrary accuracy. This solution can be coupled with<br />
anisotropic probablistic tracking to obtain scalar measures of connectivity.<br />
14:30 4010. A Minimal Model, Data-Driven Approach to Tractography<br />
Angela Downing 1 , Daniel Rueckert 2 , A David Edwards, 1,3 , Jo V. Hajnal 1<br />
1 Robert Steiner MRI Unit, Imaging Sciences Department, MRC Clinical Sciences Centre, Hammersmith<br />
Hospital, Imperial College London, London, United Kingdom; 2 Visual Information Processing Group,<br />
Department of Computing, Imperial College London, London, United Kingdom; 3 Department of Paediatrics,