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Article: Suppression of effects of gradient imperfections on imaging with alternate ascending/descending directional navigation

TitleSuppression of effects of gradient imperfections on imaging with alternate ascending/descending directional navigation
Authors
Keywordsalternate ascending/descending directional navigation
eddy current
magnetization transfer
magnetization transfer asymmetry
skeletal muscle
Issue Date2012
Citation
Magnetic Resonance in Medicine, 2012, v. 68, n. 5, p. 1600-1606 How to Cite?
AbstractAlternate ascending/descending directional navigation (ALADDIN) is a new imaging technique that provides interslice perfusion-weighted and magnetization transfer (MT) asymmetry images. In this article, we investigated the effects of gradient imperfections on ALADDIN MT asymmetry (MTA) signals. Subtraction artifacts increasing with readout offsets were detectable in ALADDIN MTA images from an agarose phantom but not from a water phantom. Slice-select offsets had no significant effect on the artifacts in MTA. The artifacts were suppressed by averaging signals over the readout gradient polarities independent of scan parameters. All these results suggested that the subtraction artifacts were induced by readout eddy currents. With suppression of the artifacts, ALADDIN signals in human brain and skeletal muscle varied less with scan conditions. Percent signal changes of MTA in human skeletal muscle (0.51 ± 0.11%, N = 3) were about 30% of those in white matter. The new averaging scheme will allow for more accurate MTA imaging with ALADDIN, especially at off-center positions. Copyright © 2012 Wiley Periodicals, Inc.
Persistent Identifierhttp://hdl.handle.net/10722/316071
ISSN
2023 Impact Factor: 3.0
2023 SCImago Journal Rankings: 1.343
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorPark, Sung Hong-
dc.contributor.authorZhao, Tiejun-
dc.contributor.authorKim, Jung Hwan-
dc.contributor.authorBoada, Fernando E.-
dc.contributor.authorBae, Kyongtae Ty-
dc.date.accessioned2022-08-24T15:49:08Z-
dc.date.available2022-08-24T15:49:08Z-
dc.date.issued2012-
dc.identifier.citationMagnetic Resonance in Medicine, 2012, v. 68, n. 5, p. 1600-1606-
dc.identifier.issn0740-3194-
dc.identifier.urihttp://hdl.handle.net/10722/316071-
dc.description.abstractAlternate ascending/descending directional navigation (ALADDIN) is a new imaging technique that provides interslice perfusion-weighted and magnetization transfer (MT) asymmetry images. In this article, we investigated the effects of gradient imperfections on ALADDIN MT asymmetry (MTA) signals. Subtraction artifacts increasing with readout offsets were detectable in ALADDIN MTA images from an agarose phantom but not from a water phantom. Slice-select offsets had no significant effect on the artifacts in MTA. The artifacts were suppressed by averaging signals over the readout gradient polarities independent of scan parameters. All these results suggested that the subtraction artifacts were induced by readout eddy currents. With suppression of the artifacts, ALADDIN signals in human brain and skeletal muscle varied less with scan conditions. Percent signal changes of MTA in human skeletal muscle (0.51 ± 0.11%, N = 3) were about 30% of those in white matter. The new averaging scheme will allow for more accurate MTA imaging with ALADDIN, especially at off-center positions. Copyright © 2012 Wiley Periodicals, Inc.-
dc.languageeng-
dc.relation.ispartofMagnetic Resonance in Medicine-
dc.subjectalternate ascending/descending directional navigation-
dc.subjecteddy current-
dc.subjectmagnetization transfer-
dc.subjectmagnetization transfer asymmetry-
dc.subjectskeletal muscle-
dc.titleSuppression of effects of gradient imperfections on imaging with alternate ascending/descending directional navigation-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/mrm.24169-
dc.identifier.pmid22287275-
dc.identifier.scopuseid_2-s2.0-84867843035-
dc.identifier.volume68-
dc.identifier.issue5-
dc.identifier.spage1600-
dc.identifier.epage1606-
dc.identifier.eissn1522-2594-
dc.identifier.isiWOS:000310062300028-

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