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Citation: M. Holschbach et al., PRECLINICAL EVALUATION OF THE NEW A(1) ADENOSINE RECEPTOR (A(1)AR) ANTAGONIST [F-18] 8-CYCLOPENTYL-1-PROPYL-3-(3-FLUOROPROPYL)XANTHINE ([F-18]CPFPX), The Journal of nuclear medicine, 39(5), 1998, pp. 77-77

Authors: HERZOG H HOLSCHBACH M BOY C WUTZ W SCHMITZ T MUHLENSIEPEN H MULLERGARTNER HW OLSSON RA COENEN HH

Citation: H. Herzog et al., BIODISTRIBUTION AND RADIATION-DOSE OF THE NEW A(1) ADENOSINE RECEPTORANTAGONIST [F-18] CPFPX IN MICE AND BABOON, The Journal of nuclear medicine, 39(5), 1998, pp. 846-846

Authors: HOLSCHBACH MH FEIN T KRUMMEICH C LEWIS RG WUTZ W SCHWABE U UNTERLUGAUER D OLSSON RA

Citation: Mh. Holschbach et al., A(1) ADENOSINE RECEPTOR ANTAGONISTS AS LIGANDS FOR POSITRON-EMISSION-TOMOGRAPHY (PET) AND SINGLE-PHOTON EMISSION TOMOGRAPHY (SPET), Journal of medicinal chemistry, 41(4), 1998, pp. 555-563

Authors: WESTER HJ BROCKMANN J ROSCH F WUTZ W HERZOG H SMITHJONES P STOLZ B BRUNS C STOCKLIN G

Citation: Hj. Wester et al., PET-PHARMACOKINETICS OF F-18 OCTREOTIDE - A COMPARISON WITH GA-67-DFO-OCTREOTIDE AND Y-86 DTPA-OCTREOTIDE, Nuclear medicine and biology, 24(4), 1997, pp. 275-286

Authors: HOLSCHBACH M FEIN T WUTZ W SCHULLER M HAMACHER K LEWIS R SCHWABE U STOCKLIN G OLSSON RA

Citation: M. Holschbach et al., NCA RADIOLABELED A(1) ADENOSINE RECEPTOR ANTAGONISTS AS LIGANDS FOR PET AND SPECT, The Journal of nuclear medicine, 37(5), 1996, pp. 625-625