File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Q-ball imaging with PROPELLER EPI acquisition

TitleQ-ball imaging with PROPELLER EPI acquisition
Authors
KeywordsKeyhole
ODF
PROPELLER
QBI
Fiber tracking
GFA
Issue Date2013
Citation
NMR in Biomedicine, 2013, v. 26, n. 12, p. 1723-1732 How to Cite?
AbstractQ-ball imaging (QBI) is an imaging technique that is capable of resolving intravoxel fiber crossings; however, the signal readout based on echo-planar imaging (EPI) introduces geometric distortions in the presence of susceptibility gradients. This study proposes an imaging technique that reduces susceptibility distortions in QBI by short-axis PROPELLER EPI acquisition. Conventional QBI and PROPELLER QBI data were acquired from two 3T MR scans of the brains of five healthy subjects. Prior to the PROPELLER reconstruction, residual distortions in single-blade low-resolution b0 and diffusion-weighted images (DWIs) were minimized by linear affine and nonlinear diffeomorphic demon registrations. Subsequently, the PROPELLER keyhole reconstruction was applied to the corrected DWIs to obtain high-resolution PROPELLER DWIs. The generalized fractional anisotropy and orientation distribution function maps contained fewer distortions in PROPELLER QBI than in conventional QBI, and the fiber tracts more closely matched the brain anatomy depicted by turbo spin-echo (TSE) T2-weighted imaging (T2WI). Furthermore, for fixed TE, PROPELLER QBI enabled a shorter scan time than conventional QBI. We conclude that PROPELLER QBI can reduce susceptibility distortions without lengthening the acquisition time and is suitable for tracing neuronal fiber tracts in the human brain. © 2013 John Wiley & Sons, Ltd.
Persistent Identifierhttp://hdl.handle.net/10722/210121
ISSN
2022 Impact Factor: 2.9
2020 SCImago Journal Rankings: 1.278
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChou, Ming Chung-
dc.contributor.authorHuang, Teng Yi-
dc.contributor.authorChung, Hsiao Wen-
dc.contributor.authorHsieh, Tsyh Jyi-
dc.contributor.authorChang, Hing Chiu-
dc.contributor.authorChen, Cheng Yu-
dc.date.accessioned2015-05-22T06:06:42Z-
dc.date.available2015-05-22T06:06:42Z-
dc.date.issued2013-
dc.identifier.citationNMR in Biomedicine, 2013, v. 26, n. 12, p. 1723-1732-
dc.identifier.issn0952-3480-
dc.identifier.urihttp://hdl.handle.net/10722/210121-
dc.description.abstractQ-ball imaging (QBI) is an imaging technique that is capable of resolving intravoxel fiber crossings; however, the signal readout based on echo-planar imaging (EPI) introduces geometric distortions in the presence of susceptibility gradients. This study proposes an imaging technique that reduces susceptibility distortions in QBI by short-axis PROPELLER EPI acquisition. Conventional QBI and PROPELLER QBI data were acquired from two 3T MR scans of the brains of five healthy subjects. Prior to the PROPELLER reconstruction, residual distortions in single-blade low-resolution b0 and diffusion-weighted images (DWIs) were minimized by linear affine and nonlinear diffeomorphic demon registrations. Subsequently, the PROPELLER keyhole reconstruction was applied to the corrected DWIs to obtain high-resolution PROPELLER DWIs. The generalized fractional anisotropy and orientation distribution function maps contained fewer distortions in PROPELLER QBI than in conventional QBI, and the fiber tracts more closely matched the brain anatomy depicted by turbo spin-echo (TSE) T2-weighted imaging (T2WI). Furthermore, for fixed TE, PROPELLER QBI enabled a shorter scan time than conventional QBI. We conclude that PROPELLER QBI can reduce susceptibility distortions without lengthening the acquisition time and is suitable for tracing neuronal fiber tracts in the human brain. © 2013 John Wiley & Sons, Ltd.-
dc.languageeng-
dc.relation.ispartofNMR in Biomedicine-
dc.subjectKeyhole-
dc.subjectODF-
dc.subjectPROPELLER-
dc.subjectQBI-
dc.subjectFiber tracking-
dc.subjectGFA-
dc.titleQ-ball imaging with PROPELLER EPI acquisition-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/nbm.3009-
dc.identifier.pmid24038670-
dc.identifier.scopuseid_2-s2.0-84888054961-
dc.identifier.volume26-
dc.identifier.issue12-
dc.identifier.spage1723-
dc.identifier.epage1732-
dc.identifier.eissn1099-1492-
dc.identifier.isiWOS:000327157400012-
dc.identifier.issnl0952-3480-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats