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A single 1,500-s 1,500-s) static PET dataset was reconstructed for all 30- to 55-min 18F-FDG scans for the scans at each time point (baseline, 5 min, 57 min, and 1, 5, and 11 weeks after ferumoxytol injection), and AC was performed using the MRAC scan immediately preceding the acquisition.
Notably, the SIENA analysis was carried out on MRI data derived from the average of three T1 volumetric scans at each time point, so providing a high degree of accuracy.
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Both breasts and axillas were scanned at each time point at the same site using a Phillips ATL HDI 5000 with a 12.5 MHz linear transducer.
Three scans were performed at each time point.
The mean signal elevations of the injured soleus muscles in the T2-weighted scans were quantified at each time point, as shown in Figure 4.
Among the subset of patients being followed in Seattle, the estimated mean decrease in T2 lesion volume from baseline to 2 years among patients with MRI scans at each of these times (n=9) was 2.7% (S.D.=19.3%, p=0.69).
Animals were scanned for 10 min at each time point (30, 60, and 120 min after injection), with the long axis of the animal parallel to the long axis of the scanner.
Each patient underwent serial scans at the time of the clinical assessments.
PET data for each mouse were recorded via static scans at various time points between 6 and 120 h.
It was initiated by performing a genome scan, or single-QTL analysis, at each time point to generate a 2D matrix of LOD scores (genomic positions × time points).
Fifteen (75%) had normal magnetic resonance imaging (MRI) and/or computed tomography (CT) scans at the time of injury.
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CEO of Professional Science Editing for Scientists @ prosciediting.com