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2013
DOI: 10.1002/jmri.24373
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T1 Mapping using variable flip angle SPGR data with flip angle correction

Abstract: The proposed method overcomes some inaccuracies in FA production, providing more accurate estimation of T1 values compared with standard methods, and is applicable for currently available data.

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Cited by 74 publications
(67 citation statements)
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References 29 publications
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“…This impression is confirmed by the numerical results in Table 3 for brain (frontal and parietal white and gray matter), liver, and kidney (cortex and medulla). Because a comprehensive determination of in vivo data for various tissues is outside the scope of this work, the present results are only compared to some most recent literature findings [16][17][18]. As it turns out all T1 values are close to published data.…”
Section: Resultssupporting
confidence: 54%
“…This impression is confirmed by the numerical results in Table 3 for brain (frontal and parietal white and gray matter), liver, and kidney (cortex and medulla). Because a comprehensive determination of in vivo data for various tissues is outside the scope of this work, the present results are only compared to some most recent literature findings [16][17][18]. As it turns out all T1 values are close to published data.…”
Section: Resultssupporting
confidence: 54%
“…The T 1 time for blood is between 1 ms to 700 ms, 700 ms to 1170 ms for white matter, 1170 ms to 1800 ms for gray matter, and 1800 ms to 5000 ms for cerebral spinal fluid based on our measurement in the NHP and the previous study in humans60.…”
Section: Methodssupporting
confidence: 52%
“…1E)59. First, the standard line fit method of VFA SPGR60 was used to calculate the pre- and post-T 1 maps after registering the 3D SPGR images of various flip angles to the IST. Then, the Gd concentration map (Fig.…”
Section: Methodsmentioning
confidence: 99%
“…In particular, the bias introduced by the spatial inhomogeneity of the radiofrequency (RF) transmit field (B1+) is a well-known source of error (Stikov et al, 2015). Numerous methods exist for obtaining a B1+ map (Insko and Bolinger, 1993; Cunningham et al, 2006; Jiru and Klose, 2006; Dowell and Tofts, 2007; Yarnykh, 2007; Lutti et al, 2010; Sacolick et al, 2010; Nehrke and Börnert, 2012) and incorporating this into the T 1 mapping pipeline has been shown to improve the accuracy of the estimated value of the T 1 relaxation times (Venkatesan et al, 1998; Deoni, 2007; Helms et al, 2008; Lutti et al, 2013; Liberman et al, 2014). However, the precision of the B1+ map and how this diminishes the precision of the estimated T 1 values has not been thoroughly addressed, especially not in vivo .…”
Section: Introductionmentioning
confidence: 99%