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EJNMMI Radiopharmacy and Chemistry|October 30, 2019
The various therapeutic applications of the medical isotope holmium-166: a narrative reviewNienke J M Klaassen, Mark J Arntz, Alexandra Gil Arranja, et al.
EJNMMI Radiopharmacy and Chemistry|December 1, 2020
Effect of the versatile bifunctional chelator AAZTA5 on the radiometal labelling properties and the in vitro performance of a gastrin releasing peptide receptor antagonistMichael Hofstetter, Euy Sung Moon, Fabio D'Angelo, et al.
EJNMMI Radiopharmacy and Chemistry|January 2, 2020
Rapid, efficient, and economical synthesis of PET tracers in a droplet microreactor: application to O-(2-[18F]fluoroethyl)-L-tyrosine ([18F]FET)Ksenia Lisova, Bao Ying Chen, Jia Wang, et al.
EJNMMI Radiopharmacy and Chemistry|November 10, 2020
Automated synthesis of 18F radiolabelled indole containing Oncrasin-like molecules; a comparison of iodonium salts and boronic ester chemistryAlexander F McDonald, Yit Wooi Goh, Jonathan M White, et al.
EJNMMI Radiopharmacy and Chemistry|November 11, 2020
Use of 55 PET radiotracers under approval of a Radioactive Drug Research Committee (RDRC)Isaac M Jackson, So Jeong Lee, Alexandra R Sowa, et al.
EJNMMI Radiopharmacy and Chemistry|July 23, 2022
Development of new copper-64 labeled rhodamine: a potential PET myocardial perfusion imaging agentNorah AlHokbany, Ibrahim AlJammaz, Basem AlOtaibi, et al.
EJNMMI Radiopharmacy and Chemistry|March 13, 2018
Synthesis, gallium labelling and characterization of P04087, a functionalized phosphatidylserine-binding peptideRana Ben Azzouna, Alexandre Guez, Khadija Benali, et al.
EJNMMI Radiopharmacy and Chemistry|March 6, 2018
Production of novel diagnostic radionuclides in small medical cyclotronsMateusz Adam Synowiecki, Lars Rutger Perk, J Frank W Nijsen
EJNMMI Radiopharmacy and Chemistry|March 6, 2018
Synthesis of an Al18F radiofluorinated GLU-UREA-LYS(AHX)-HBED-CC PSMA ligand in an automated synthesis platformJavier Giglio, Maia Zeni, Eduardo Savio, et al.
EJNMMI Radiopharmacy and Chemistry|June 12, 2018
Comparison of fully-automated radiosyntheses of [11C]erlotinib for preclinical and clinical use starting from in target produced [11C]CO2 or [11C]CH4Cécile Philippe, Severin Mairinger, Verena Pichler, et al.
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