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IDEAL knee MRI data is proposed. Variation in the characteristics of similar structures in IDEAL water and fat images is used to<br />

generate the guidance map for automated segmentation. Segmented structures are analyzed qualitatively and quantitatively with<br />

manually segmented datasets from GE 1.5T scanner. Reported DSC with the experimental datasets (>85%) indicates that the proposed<br />

solution improved the robustness of segmentation.<br />

Contrast Mechanisms<br />

Hall B Monday 14:00-16:00 Computer 127<br />

14:00 5119. The Effect of NMR-Invisible Susceptibility Inclusions on Phase Maps.<br />

Samuel James Wharton 1 , Richard Bowtell 1<br />

1 Sir Peter Mansfield Magnetic Resonance Centre, University of Nottingham, Nottingham, United Kingdom<br />

Phase images generated at high field show exquisite anatomical contrast resulting from small changes of the NMR frequency linked to<br />

variation of the local magnetic susceptibility across tissues. When a significant contribution to the average susceptibility comes from<br />

NMR-invisible inclusions, the average NMR frequency offset is not however simply proportional to the average susceptibility. Here,<br />

we derive a simple expression based on the use of the conventional sphere of Lorentz, which allows the average NMR frequency<br />

offset to be calculated for compartments containing inclusions of varying shape and concentration. The expression is tested by<br />

comparison with the results of simulations.<br />

14:30 5120. MRI Signal Response Mapping (SIRMA) to Dephaser to Quantify Susceptibility<br />

Gradient<br />

florence franconi 1 , Jean-Jacques Le Jeune 2 , Pascal Richomme 1 , Laurent Lemaire 2<br />

1 PIAM, Université d'Angers, Angers, France, Metropolitan; 2 UMR-S646, INSERM, Angers, France<br />

SIgnal Response MApping to dephaser (SIRMA) method is proposed to quantify susceptibility gradient. In gradient echo acquisitions,<br />

the SIRMA method measures the echo shifts in k-space of susceptibility affected spins from a series of dephased images collected<br />

with additional incremental slice refocusing gradient offset or incremental reconstruction window off-centering. SIRMA applicability<br />

and performances have been demonstrated in vitro through quantization of susceptibility gradient induced in a cylinder model and in<br />

vivo through the quantitative detection of SPIO distribution volume. With respect to its quantitative nature, its computational<br />

simplicity, this method deserves further attention for application in molecular or cellular imaging.<br />

15:00 5121. Simultaneous δR1 and δR2* Quantification in 5s to Monitor Blood and Tissue<br />

Oxygenation with Dynamic (C)O 2 Enhanced MRI<br />

Stefanie Remmele 1 , Tobias Voigt 2 , Jochen Keupp 1 , Christian Stehning 1 , Julien Sénégas 1<br />

1 Philips Research Europe, Hamburg, Germany; 2 University of Karlsruhe, Karlsruhe, Germany<br />

This work presents an approach to simultaneous and dynamic dR1, dR2* estimation that combines the beneficial features of currently<br />

used techniques for dynamic R1 quantification in DCE-MRI and for dynamic R2*-quantification in D(C)O2E-MRI. The technique<br />

aims at increasing the specificity of R2* BOLD imaging during respiratory challenges. Its accuracy and sensitivity is evaluated in<br />

phantom and breathold experiments.<br />

15:30 5122. Susceptibility Weighted Imaging and Susceptibility Mapping (SWIM): A New<br />

Means to Visualize Veins and Quantify Susceptibility<br />

Ewart Mark Haacke 1,2 , Jin Tang 3 , Yu-Chung Norman Cheng 1 , Jaladhar Neelavalli 2,4<br />

1 Academic Radiology, Wayne State University, Detroit, MI, United States; 2 The MRI Institute for Biomedical<br />

Research, Detroit, MI, United States; 3 McMaster University, Hamilton, Ontario, Canada; 4 Nuffield Department<br />

of Surgery, University of Oxford, Oxford, United Kingdom<br />

A new means of visualizing veins which is independent of orientation of vessels (or the head) relative to the main magnetic field is<br />

presented. This new venous imaging method is based on direct mapping of the susceptibility using the inverse Green’s function<br />

approach.<br />

Tuesday 13:30-15:30 Computer 127<br />

13:30 5123. Feasibility of Brain Lesion Characterization at 1.5T – Whole-Brain Susceptibility<br />

Mapping Using A Homogeneous Lesion Constraint<br />

Ferdinand Schweser 1 , Andreas Deistung 2 , Berengar Wendel Lehr 2 , Jürgen Rainer<br />

Reichenbach 2<br />

1 Medical Physics Group, Department of Diagnostic and Interventional Radiology , Jena University Hospital,<br />

Jena, Germany; 2 Medical Physics Group, Department of Diagnostic and Interventional Radiology, Jena<br />

University Hospital, Jena, Germany<br />

A method is presented for high-quality whole-brain susceptibility mapping based on standard clinical single-shot low-field SWI-data.<br />

Feasibility of in-vivo lesion characterization is demonstrated for clinical patient data.

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