08.03.2014 Views

ELECTRONIC POSTER - ismrm

ELECTRONIC POSTER - ismrm

ELECTRONIC POSTER - ismrm

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

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,

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!