https://www.selleckchem.com/pr....oducts/pd0166285.htm
Predicted and true clinical absorbed doses for [18F]FDG and [18F]AlF-NOTA-OC were then used to quantify bias of preclinical model predictions versus clinical measurements. Our results show that most dosimetry models were biased in their predicted clinical dosimetry compared to empirical values. Therefore, normalization of rathuman organ sizes and correction for reconstruction method biases are required to achieve higher precision of dosimetry estimates.In many species, excitable cells preserve their physiological properties despite si
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