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1 the monoamine oxidase inhibitor selegiline (L-deprenyl).
2 2 is a better index of MAO activity than 11C-L-deprenyl.
3 ly larger for 11C-L-deprenyl-D2 than for 11C-L-deprenyl.
6 , and healthy controls using (11)C-deuterium-L-deprenyl ((11)C-DED) to measure monoamine oxidase B lo
8 not confirm previous findings that low dose L-deprenyl administration in vivo after MPTP can rescue
10 nd the monoamine oxidase B (MAO-B) inhibitor L-deprenyl, alone and in combination, on striatal dopami
11 radiolabel a novel bis-deuterium substituted l-deprenyl analog (fluorodeprenyl-D2) with (18)F and to
12 studies of the torso area 2 h apart with 11C-L-deprenyl and deuterium-substituted 11C-L-deprenyl (11C
14 Addition of the monoamine (MAO) inhibitors, l-deprenyl, clorgyline, pargyline, or in vivo nialamide
20 evels of MAO B is improved by the use of 11C-L-deprenyl-D2, similar to prior studies on the brain.
21 Pittsburgh compound-B (PIB), (11)C-deuterium-L-deprenyl (DED) and (18)F-fluorodeoxyglucose (FDG) resp
22 ly, monoamine oxidase blockers pargyline and l-deprenyl had no effect on DAcyt levels in MPP(+)-treat
25 anti-parkinsonian medications which include L-deprenyl, it will be important to further investigate
26 Combined effects of uptake inhibitors with l-deprenyl on dopamine clearance were additive (up to 99
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