2000
DOI: 10.1006/nimg.2000.0607
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Regularization of Diffusion-Based Direction Maps for the Tracking of Brain White Matter Fascicles

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Cited by 388 publications
(303 citation statements)
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“…2,3 Various groups have used DTT to track fibers in fixed rodent brain 1,25 and in living humans. [2][3][4][5]26 Physical basis of using DT-MRI to track ®bers DTT is based on diffusion tensor-encoded MRI (DT-MRI), in which diffusion-weighted imaging (DWI) data are acquired for computing the effective diffusion tensor 27 and its derived properties such as directionally averaged diffusion 28,29 and anisotropy. [30][31][32][33] Early DWI studies observed a faster diffusion along the WM fibers, [34][35][36] thought to be due in part to membranes that slow diffusion perpendicular to the fiber.…”
Section: Biological Backgroundmentioning
confidence: 99%
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“…2,3 Various groups have used DTT to track fibers in fixed rodent brain 1,25 and in living humans. [2][3][4][5]26 Physical basis of using DT-MRI to track ®bers DTT is based on diffusion tensor-encoded MRI (DT-MRI), in which diffusion-weighted imaging (DWI) data are acquired for computing the effective diffusion tensor 27 and its derived properties such as directionally averaged diffusion 28,29 and anisotropy. [30][31][32][33] Early DWI studies observed a faster diffusion along the WM fibers, [34][35][36] thought to be due in part to membranes that slow diffusion perpendicular to the fiber.…”
Section: Biological Backgroundmentioning
confidence: 99%
“…[40][41][42][43] Information on the direction of fastest diffusion has formed the basis for reconstructing the 3D trajectories of WM fiber bundles. [1][2][3][4][5]25,26 In DTT, the three-dimensional trajectory of a WM pathway (a tract) is approximated by a set of computed lines representing the trajectories of fastest water diffusion (the tracks). The WM pathways in Conturo et al 3 empirically contained typically $20-500 tracks.…”
Section: Biological Backgroundmentioning
confidence: 99%
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“…By comparing this information with conventional MR parameter maps, we can identify specific white matter tracts that are affected by the lesions. We can extend this approach in a more systematic way by identifying the 3D trajectories of individual white matter tracts using 3D tract reconstruction, or tractography (Conturo et al, 1999;Mori et al, 1999;Basser et al, 2000;Poupon et al, 2000;Parker et al, 2002). Once a tract of interest is defined in three dimensions, we can superimpose its coordinates on MR parameter maps to perform quantitative tract-specific monitoring of pathological conditions (Virta et al, 1999;Xue et al, 1999;Stieltjes et al, 2001;Glenn et al, 2003;Wilson et al, 2003;Partridge et al, 2004;Pagani et al, 2005).…”
Section: Introductionmentioning
confidence: 99%
“…[25][26][27] However, it was not until the end of the decade and the beginning of the new millenium that the first successful in vivo fiber tracking results were published. [28][29][30][31][32][33][34][35][36][37][38][39][40][41][42] The reason for this time lag between the availability of the tensor diagonalization techniques that provide the vector information and the actual mapping of the fibers is due to the inherent complexity of connecting these macroscopic voxel-based vectors in a reproducible three-dimensional manner. At present, new tracking algorithms are being developed rapidly, and in this review we will provide an overview of the current state-of-the-art approaches.…”
Section: Introductionmentioning
confidence: 99%