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Limitations of [F]MISO PET include the modest signal-to-noise ratio of raw [F]MISO PET images but if a venous blood sample is acquired during the mid-course of the imaging procedure and used to calculate a tumour /blood (T /B) ratio image, then normoxic uptake (T /B < 1) can be electronically subtracted to increase image contrast.
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Blood samples were acquired to evaluate hormonal concentrations, and premenstrual symptoms were assessed through daily record of severity of problems questionnaires.
This retrospective study has the principal limitation that no blood samples were acquired.
Arterialised-venous blood samples were acquired at 45 min and 2 and 4 h time-points post tracer injection [33].
Arterial blood samples were acquired during the first 90 min, and both the plasma- and whole blood volume-corrected tracer contents were measured using the well counter.
Dynamic [11C]PBR28 PET imaging data with arterial blood sampling were acquired to quantify TSPO levels as [11C]PBR28 V T. Scans were acquired at three timepoints: baseline, immediately post-drug, and prolonged post-drug.
Blood samples were acquired from patients of the University of California at Davis William R. Pritchard Veterinary Medical Teaching Hospital.
All blood samples were acquired before any therapeutic intervention.
Overnight fasting blood samples were acquired for laboratory measurements.
Peripheral blood samples were acquired before and after mammography.
Following an overnight fast, blood samples were acquired in the morning from each subject.
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