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[18F]-PBR111 vofume of distribution (V t) in volume of interests (VOIs) was quantified by means of kinetic modelling and a VOI/metabolite-corrected plasma activity ratio.
Recent studies have attempted to take advantage of morphological features and dynamic information: dynamic and morphological data, generally separately, have been used both for segmentation of volume of interests (VOIs) [7, 8, 9, 10, 11] and for lesion classification [6, 7, 8, 9, 10, 11, 12, 13, 14, 15].
Volume of interests (VOI) was based on the estimated tumor volume from T1-weighted MR images, and centered at an anatomical landmark in reference to the inoculation coordinates.
The total cylinder volume of interests (VOIs-T) (4.8 mm in diameter and 10 mm in height) including osteochondral composite was selected from the reconstructed datasets.
Cylindrical volume of interests with a mean diameter of 3.1 mm and mean height of 2.2 mm were created to isolate the defect.
Then, a cylinder ceramic volume of interests (VOIs-C) was established using the same center of the bottom cycle surface with 4.8 mm in diameter and 6mm in height.
Similar(54)
Two major volume-of-interests (VOIs) were defined on the MRI template, one comprising the full cortex including hippocampus, the other comprising the full cerebellum.
Recovery coefficients (RCs) were measured for clinically used volume-of-interest definitions.
A volume-of-interest (VOI) was created for each lesion over the segmented PET images.
Volume-of-interest analysis was used to assess TSSP-related brain activation.
Vascular tortuosity was computed from tumor regions with predefined volume-of-interest based on tumor volume.
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