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The superiority of combined SPECT/CT over conventional SPECT and planar scintigraphy in bone scans has been shown in various studies [10 12].
Nevertheless, a correlation between EDPs and lung damage on computed tomographic scans has been shown [ 9].
Importantly, vascular inflammation seen on FDG-PET/CT scans has been shown to precede the development of atherosclerotic disease [ 10] and to predict future cardiovascular events [ 11, 12].
Concordant negative GM-EIA together with thoracic CT scans has been shown to have the highest discriminatory power to exclude IPA as a diagnosis.
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Bone mineral density (BMD) measurements acquired from quantitative computed tomography scans have been shown to correlate with bone mechanical properties such as strength, stiffness, and yield load.
CT scans have been shown to be more reliable than X-rays in quantifying articular surface incongruencies [6, 7, 8, 9, 10].
For example, in a recent study by our group, MFR of 41 patients calculated from independent CMR and PET scans have been shown to correlate well, however absolute CMR perfusion at stress and rest correlated weakly and were positively biased compared to their PET counterparts (Morton et al., 2012).
MRI scans have been shown to be particularly useful in the assessment of retropharyngeal and cervical lymphadenopathy [ 7].
Metaiodobenzylguanidine scans have been shown to be the most sensitive method for detecting both residual bone disease and unsuspected asymptomatic relapse in high-risk neuroblastoma (Kushner et al, 2009; Taggart et al, 2009).
Results of MRI scans have been shown to alter clinical decisions regarding management of rotator cuff tears in the orthopaedic setting [ 52] and MRA may therefore be indicated at the primary care level if there is clinical suspicion of rotator cuff disruption in the presence of equivocal ultrasound findings.
Fat-suppressed, T1-weighted, three-dimensional, gradient-echo scans have been shown to delineate articular cartilage accurately in various joints, including the MCPs [ 22], and are commercially available on all clinical MRI systems operating at magnetic field strengths of 1.0 T or higher.
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CEO of Professional Science Editing for Scientists @ prosciediting.com