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CT has absolute (100%%) sensitivity for the detection of retroperitoneal haematomas, which appear as more or less hyperattenuating (35 to 70 Hounsfield units) collections on precontrast scans depending on their more or less acute stage.
Conversely, clinically significant iatrogenic haematomas appear as hyperattenuating collections (45 to 90 Hounsfield Units, HU) on precontrast scans depending on their more or less acute stage, being relatively hyperdense compared to the renal parenchyma (Figs. 3, 4, 5 and 6).
In their 2007 study, Tayal et al. [11] concluded that this technique can be learned relatively quickly with a learning curve of between 10 and 25 scans depending on previous ultrasound experience.
NMR spectra were acquired at 20 °C for 2048 direct and 256 of 400 indirect data points with 16 or 32 scans depending on the peptide concentration.
After visual inspection, manual editing of any errors is needed in less than 10%% of scans, depending on the type of post-processing.
For one-dimensional (1D) H NMR, typical experimental conditions included 32K data points, a sweep width of 13 ppm, a recycle delay of 1.5 s, and 32−256 scans depending on sample concentration.
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Furthermore, X-ray absorption during CT scans depends on physical density and based on grey value differences (du Plessis et al. 2013; Lindgren et al. 2016).
The detectability of low-contrast features in PET scans depends on count statistics, which in turn depend on various factors including the efficiency of the scanner, administered activity, uptake time, acquisition time and the size of the patient.
These image scans depend on the cellular ability to uptake either iodide or glucose.
The exact number of scans depended on the participants' viewing behavior and the calibration procedure, and ranged from 197 to 359 scans (M = 224 scans, SD = 27 scans).
The resolution of the scans depended on the material: 21 or 33 μm for prepared bone, 33 μm for alcohol preserved/fresh specimens, and 38 μm for anesthetized mice to keep the X-ray dosage low.
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