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Reading
NeuroRx. 2005 Apr ;2 (2):167-96 15897944
[Cited:
8] |
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Foundations of advanced magnetic resonance imaging.
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[My paper]
Roland
Bammer ,
Stefan
Skare ,
Rexford
Newbould ,
Chunlei
Liu ,
Vincent
Thijs ,
Stefan
Ropele ,
David B
Clayton ,
Gunnar
Krueger ,
Michael
E Moseley ,
Gary H
Glover |
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During the past decade, major breakthroughs in
magnetic resonance imaging (MRI) quality were made by means of
quantum leaps in scanner hardware and pulse sequences. Some advanced
MRI techniques have truly revolutionized the detection of disease
states and MRI can now-within a few minutes-acquire important
quantitative information noninvasively from an individual in any
plane or volume at comparatively high resolution. |
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Nat Neurosci. 2003 Jul ;6 (7):750-7 12808459
[Cited:
3] |
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Non-invasive mapping of connections between human thalamus and
cortex using diffusion imaging.
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[My paper]
T E J
Behrens ,
H
Johansen-Berg ,
M W
Woolrich ,
S M
Smith ,
C A M
Wheeler-Kingshott ,
P A
Boulby ,
G J
Barker ,
E L
Sillery ,
K
Sheehan ,
O
Ciccarelli ,
A J
Thompson ,
J M
Brady ,
P M
Matthews |
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Evidence concerning anatomical connectivities in the
human brain is sparse and based largely on limited post-mortem
observations. Diffusion tensor imaging has previously been used to
define large white-matter tracts in the living human brain, but this
technique has had limited success in tracing pathways into gray
matter. Here we identified specific connections between human
thalamus and cortex using a novel probabilistic tractography
algorithm with diffusion imaging data. Classification of thalamic
gray matter based on cortical connectivity patterns revealed
distinct subregions whose locations correspond to nuclei described
previously in histological studies. The connections that we found
between thalamus and cortex were similar to those reported for
non-human primates and were reproducible between individuals. Our
results provide the first quantitative demonstration of reliable
inference of anatomical connectivity between human gray matter
structures using diffusion data and the first connectivity-based
segmentation of gray matter. |
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Magn Reson Med. 2004 Dec ;52 (6):1358-72 15562495
[Cited:
2] |
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Q-ball
imaging. |
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[My paper]
David S
Tuch |
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Magnetic resonance diffusion tensor imaging (DTI)
provides a powerful tool for mapping neural histoarchitecture in
vivo. However, DTI can only resolve a single fiber orientation
within each imaging voxel due to the constraints of the tensor
model. For example, DTI cannot resolve fibers crossing, bending, or
twisting within an individual voxel. Intravoxel fiber crossing can
be resolved using q-space diffusion imaging, but q-space imaging
requires large pulsed field gradients and time-intensive sampling.
It is also possible to resolve intravoxel fiber crossing using
mixture model decomposition of the high angular resolution diffusion
imaging (HARDI) signal, but mixture modeling requires a model of the
underlying diffusion process.Recently, it has been shown that the
HARDI signal can be reconstructed model-independently using a
spherical tomographic inversion called the Funk-Radon transform,
also known as the spherical Radon transform. The resulting imaging
method, termed q-ball imaging, can resolve multiple intravoxel fiber
orientations and does not require any assumptions on the diffusion
process such as Gaussianity or multi-Gaussianity. The present paper
reviews the theory of q-ball imaging and describes a simple linear
matrix formulation for the q-ball reconstruction based on spherical
radial basis function interpolation. Open aspects of the q-ball
reconstruction algorithm are discussed. |
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Neuron. 2003 Dec 4;40 (5):885-95 14659088
[Cited:
2] |
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Diffusion
MRI of complex neural architecture.
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[My paper]
David S Tuch
,
Timothy G
Reese ,
Mette R
Wiegell ,
Van J Wedeen
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While functional brain imaging methods can locate the
cortical regions subserving particular cognitive functions, the
connectivity between the functional areas of the human brain remains
poorly understood. Recently, investigators have proposed a method to
image neural connectivity noninvasively using a magnetic resonance
imaging method called diffusion tensor imaging (DTI). DTI measures the
molecular diffusion of water along neural pathways. Accurate
reconstruction of neural connectivity patterns from DTI has been
hindered, however, by the inability of DTI to resolve more than a single
axon direction within each imaging voxel. Here, we present a novel
magnetic resonance imaging technique that can resolve multiple axon
directions within a single voxel. The technique, called q-ball imaging,
can resolve intravoxel white matter fiber crossing as well as white
matter insertions into cortex. The ability of q-ball imaging to resolve
complex intravoxel fiber architecture eliminates a key obstacle to
mapping neural connectivity in the human brain noninvasively.
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NMR Biomed. ;15 (7-8):468-80 12489096
[Cited:
2] |
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Fiber
tracking: principles and strategies - a technical review.
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[My paper]
Susumu
Mori ,
Peter C
M van Zijl |
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The state of the art of reconstruction of the axonal
tracts in the central nervous system (CNS) using diffusion tensor
imaging (DTI) is reviewed. This relatively new technique has
generated much enthusiasm and high expectations because it presently
is the only approach available to non-invasively study the
three-dimensional architecture of white matter tracts. While there
is no doubt that DTI fiber tracking is providing exciting new
opportunities to study CNS anatomy, it is very important to
understand its limitations. In this review we therefore assess the
basic principles and the assumptions that need to be made for each
step of the study, including both data acquisition and the elaborate
fiber reconstruction algorithms. Special attention is paid to
situations where complications may arise, and possible solutions are
reviewed. Validation issues and potential future directions and
improvements are also discussed. |
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Neurobiol Aging. ;26 (8):1215-27 15917106
[Cited:
1] |
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Age-related alterations in white matter microstructure measured by
diffusion tensor imaging.
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[My paper]
D H
Salat ,
D S Tuch
,
D N
Greve ,
A J W
van der Kouwe ,
N D
Hevelone ,
A K
Zaleta ,
B R
Rosen ,
B Fischl
,
S Corkin
,
H Diana
Rosas ,
A M Dale
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Cerebral white matter (WM) undergoes various
degenerative changes with normal aging, including decreases in
myelin density and alterations in myelin structure. We acquired
whole-head, high-resolution diffusion tensor images (DTI) in 38
participants across the adult age span. Maps of fractional
anisotropy (FA), a measure of WM microstructure, were calculated for
each participant to determine whether particular fiber systems of
the brain are preferentially vulnerable to WM degeneration. Regional
FA measures were estimated from nine regions of interest in each
hemisphere and from the genu and splenium of the corpus callosum
(CC). The results showed significant age-related decline in FA in
frontal WM, the posterior limb of the internal capsule (PLIC), and
the genu of the CC. In contrast, temporal and posterior WM was
relatively preserved. These findings suggest that WM alterations are
variable throughout the brain and that particular fiber populations
within prefrontal region and PLIC are most vulnerable to age-related
degeneration. |
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