Introduction to diffusion tensor imaging /

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Bibliographic Details
Author / Creator:Mori, S. (Susumu)
Edition:1st ed.
Imprint:Amsterdam ; Boston : Elsevier, 2007.
Description:xiii, 176 p. : ill. (chiefly ill.) ; 31 cm.
Language:English
Subject:
Format: Print Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/6686401
Hidden Bibliographic Details
ISBN:9780444528285 (alk. paper)
0444528288 (alk. paper)
Notes:Includes bibliographical references (p. 163-173) and index.
Table of Contents:
  • Preface
  • Chapter 1. Basics of diffusion measurement
  • 1.1. NMR spectroscopy and MRI can detect signals from water molecules
  • 1.2. What is diffusion?
  • 1.3. How to measure diffusion?
  • Chapter 2. Anatomy of diffusion measurement
  • 2.1. A set of unipolar gradients and spin-echo sequence is most widely used for diffusion weighting
  • 2.2. There are four parameters that affect the amount of signal loss
  • 2.3. There are several ways of achieving a different degree of diffusion weighting
  • Chapter 3. Mathematics of diffusion measurement
  • 3.1. We need to calculate distribution of signal phases by molecular motion
  • 3.2. Simple exponential decay describes signal loss by diffusion weighting
  • 3.3. Diffusion constant can be obtained from the amount of signal loss but not from the signal intensity
  • 3.4. From two measurements, we can obtain a diffusion constant
  • 3.5. If there are more than two measurement points, linear least-square fitting is used
  • Chapter 4. Principle of diffusion tensor imaging
  • 4.1. NMR/MRI can measure diffusion constants along an arbitrary axis
  • 4.2. Diffusion sometimes has directionality
  • 4.3. Six parameters are needed to uniquely define an ellipsoid
  • 4.4. Diffusion tensor imaging characterizes the diffusion ellipsoid from multiple diffusion constant measurements along different directions
  • 4.5. Water molecules probe microscopic properties of their environment
  • 4.6. Human brain white matter has high diffusion anisotropy
  • Chapter 5. Mathematics of diffusion tensor imaging
  • 5.1. Our task is to determine six parameters of a diffusion ellipsoid
  • 5.2. We can obtain the six parameters from seven diffusion measurements
  • 5.3. Determination of the tensor elements from a fitting process
  • Chapter 6. Practical aspects of diffusion tensor imaging
  • 6.1. Two types of motion artifacts: ghosting and coregistration error
  • 6.2. We use echo-planar imaging to perform diffusion tensor imaging
  • 6.3. The amount of diffusion-weighting is constrained by the echo time
  • 6.4. There are various k-space sampling schemes
  • 6.5. Parallel imaging is good news for DTI
  • 6.6. Image distortion by eddy current needs special attention
  • 6.7. DTI results may differ if spatial resolution and SNR are not the same
  • 6.8. Selection of b-matrix
  • Chapter 7. New image contrasts from diffusion tensor imaging: theory, meaning, and usefulness of DTI-based image contrast
  • 7.1. Two scalar maps (anisotropy and diffusion constant maps) and fiber orientation maps are important outcomes obtained from DTI
  • 7.2. Scalar maps (anisotropy and diffusion constant maps) and fiber orientation maps are two important images obtained from DTI
  • 7.3. There are tubular and planar types of anisotropy
  • 7.4. DTI has several disadvantages
  • 7.5. There are multiple sources that decrease anisotropy
  • 7.6. Anisotropy may provide unique information
  • 7.7. Color-coded maps are a powerful visualization method to reveal white matter anatomy
  • Chapter 8. Limitations and improvement of diffusion tensor imaging
  • 8.1. Tensor model oversimplifies the underlying anatomy
  • 8.2. There are more sophisticated "non-tensor"-based data processing methods, which require different data acquisition protocols
  • 8.3. Non-tensor models usually require high b-values
  • Chapter 9. Three-dimensional tract reconstruction
  • 9.1. Three-dimensional trajectories can be reconstructed from DTI data
  • 9.2. There are two types of reconstruction techniques
  • 9.3. There are three steps in the tract propagation models
  • 9.4. Simple streamline tracking can be used to reconstruct a tract
  • 9.5. There are many limitations to simple tract propagation methods
  • 9.6. Several approaches are proposed to tackle the limitations
  • 9.7. Tract editing uses multiple regions of interest
  • 9.8. Brute-force approach is an effective technique for comprehensive tract reconstruction
  • 9.9. Accuracy and precision are important factors to be considered
  • 9.10. Reproducibility of tractography is measurable
  • 9.11. Tractography reveals macroscopic white matter anatomy
  • 9.12. There are roughly three types of information obtained from tractography
  • 9.13. How can we validate tractography?
  • 9.14. How should we use a tool with unknown accuracy?
  • 9.15. Quantification is a key to many types of tractography-based studies
  • 9.16. There are several possible reasons that lead to smaller (or larger) reconstruction results
  • Chapter 10. Quantification approaches
  • 10.1. Improvement of conventional quantification approaches
  • 10.2. Quantification of anisotropy and tract sizes by DTI
  • Chapter 11. Application studies
  • 11.1. Background of application studies of DTI
  • 11.2. Examples of application studies
  • References and Suggested Readings
  • Subject Index