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At center A (the training dataset), whole body PET/CT imaging was acquired approximately 90 min later.
Although a simultaneous PET-MRI system was used which provides inherent co-registration, the TOF-MRA data for segmentation of arteries was acquired approximately 20 to 30 min prior to the PET acquisition.
The PET/CT scan was acquired approximately 60 min after tracer injection.
Each F-FDG-PET/CT was acquired approximately 60 minutes (mean: 62 min, range: 56 min – 70 min) after the intravenous administration of approximately 20 mCi F-FDG (mean: 20.1 mCi, range 17.6 mCi – 22.1 mCi).
After the mice were anesthetized, 2 mg of d-luciferin in 200 μL of PBS solution was administered into the mice by tail vein injection, and then bioluminescence imaging was acquired approximately 10 min after luciferin administration on an IVIS Lumina II optical system (Caliper Life Science, MA, USA).
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Points were acquired approximately 172 meters apart along the satellite's flight path, which included both ascending and descending tracks on an orbit with a 94° declination [12].
Around 250,000 events in the gate R1 were acquired (approximately 290,000 total events), and a minimum of 100 CD34+ events were collected, according to recommendations.
Repeat planar and SPECT studies were acquired approximately 4 h after injection.
Points were acquired approximately 172 meters apart along the satellite's flight path, which included both ascending and descending tracks on an orbit with a 94° declination [ 12].
Transmission CT images for attenuation correction and lesion localization, and PET emission images, were acquired approximately 1 hour after injection using a Biograph PET/CT system (Siemens).
Patients were administered a weight-adjusted dosed of fluorine-18 FDG (5.18 MBq/kg), and images were acquired approximately 60 minutes (range: 50-75 minutes) after an intravenous injection of fluorine-18 FDG.
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