A P Wolf|J S Fowler - JoVE Visualize

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Journal of Medicinal Chemistry|July 1, 1990

Synthesis of (R)-(-)- and (S)-(+)-4-fluorodeprenyl and (R)-(-)- and (S)-(+)-[N-11C-methyl]-4-fluorodeprenyl and positron emission tomography studies in baboon brainA Plenevaux, S L Dewey, J S Fowler, et al.

International Journal of Radiation Applications and Instrumentation. Part A, Applied Radiation and Isotopes|January 1, 1991

The synthesis of no-carrier-added DL-4-[18F]fluorodeprenyl via the nucleophilic aromatic substitution reactionA Plenevaux, J S Fowler, S L Dewey, et al.

Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|February 1, 1985

Syntheses and specific activity determinations of no-carrier-added (NCA) F-18-labeled butyrophenone neuroleptics--benperidol, haloperidol, spiroperidol, and pipamperoneC Y Shiue, J S Fowler, A P Wolf, et al.

Biological Psychiatry|October 1, 1984

Mapping brain neuroleptic receptors in the live baboonC D Arnett, J S Fowler, A P Wolf, et al.

Applied Radiation and Isotopes : Including Data, Instrumentation and Methods for Use in Agriculture, Industry and Medicine|April 1, 1993

Rapid radiochemical and chemical quality control of [11C]putrescineS J Gatley, R A Ferrieri, J S Fowler, et al.

Journal of Medicinal Chemistry|February 1, 1991

Synthesis of high specific activity (+)- and (-)-6-[18F]fluoronorepinephrine via the nucleophilic aromatic substitution reactionY S Ding, J S Fowler, S J Gatley, et al.

Journal of Medicinal Chemistry|March 1, 1976

Radiopharmaceuticals. 16. Halogenated dopamine analogs. Synthesis and radiolabeling of 6-iododopamine and tissue distribution studies in animalsJ S Fowler, R R MacGregor, A P Wolf, et al.

Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|January 1, 1987

Fluorine-18-N-methylspiroperidol: radiolytic decomposition as a consequence of high specific activity and high dose levelsR R MacGregor, D J Schlyer, J S Fowler, et al.

Life Sciences|April 8, 1985

[18F]-N-Methylspiroperidol: the radioligand of choice for PETT studies of the dopamine receptor in human brainC D Arnett, J S Fowler, A P Wolf, et al.

Journal of Neurochemistry|March 1, 1985

Comparison of three 18F-labeled butyrophenone neuroleptic drugs in the baboon using positron emission tomographyC D Arnett, C Y Shiue, A P Wolf, et al.

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Journal of Medicinal Chemistry|July 1, 1990

Synthesis of (R)-(-)- and (S)-(+)-4-fluorodeprenyl and (R)-(-)- and (S)-(+)-[N-11C-methyl]-4-fluorodeprenyl and positron emission tomography studies in baboon brainA Plenevaux, S L Dewey, J S Fowler, et al.

International Journal of Radiation Applications and Instrumentation. Part A, Applied Radiation and Isotopes|January 1, 1991

The synthesis of no-carrier-added DL-4-[18F]fluorodeprenyl via the nucleophilic aromatic substitution reactionA Plenevaux, J S Fowler, S L Dewey, et al.

Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|February 1, 1985

Syntheses and specific activity determinations of no-carrier-added (NCA) F-18-labeled butyrophenone neuroleptics--benperidol, haloperidol, spiroperidol, and pipamperoneC Y Shiue, J S Fowler, A P Wolf, et al.

Biological Psychiatry|October 1, 1984

Mapping brain neuroleptic receptors in the live baboonC D Arnett, J S Fowler, A P Wolf, et al.

Applied Radiation and Isotopes : Including Data, Instrumentation and Methods for Use in Agriculture, Industry and Medicine|April 1, 1993

Rapid radiochemical and chemical quality control of [11C]putrescineS J Gatley, R A Ferrieri, J S Fowler, et al.

Journal of Medicinal Chemistry|February 1, 1991

Synthesis of high specific activity (+)- and (-)-6-[18F]fluoronorepinephrine via the nucleophilic aromatic substitution reactionY S Ding, J S Fowler, S J Gatley, et al.

Journal of Medicinal Chemistry|March 1, 1976

Radiopharmaceuticals. 16. Halogenated dopamine analogs. Synthesis and radiolabeling of 6-iododopamine and tissue distribution studies in animalsJ S Fowler, R R MacGregor, A P Wolf, et al.

Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|January 1, 1987

Fluorine-18-N-methylspiroperidol: radiolytic decomposition as a consequence of high specific activity and high dose levelsR R MacGregor, D J Schlyer, J S Fowler, et al.

Life Sciences|April 8, 1985

[18F]-N-Methylspiroperidol: the radioligand of choice for PETT studies of the dopamine receptor in human brainC D Arnett, J S Fowler, A P Wolf, et al.

Journal of Neurochemistry|March 1, 1985

Comparison of three 18F-labeled butyrophenone neuroleptic drugs in the baboon using positron emission tomographyC D Arnett, C Y Shiue, A P Wolf, et al.

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