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1 al features were striking and reminiscent of diffuse Lewy body disease.
2 y bodies in sporadic Parkinson's disease and diffuse Lewy body disease.
3 absence of delusions distinguished PSP from diffuse Lewy body disease.
4 ting activity in a pattern characteristic of diffuse Lewy body disease.
5 ra of Parkinson disease and the neocortex of diffuse Lewy body disease.
6 with motor and cognitive deficits similar to diffuse Lewy body disease.
7 of PD and in brains of patients with PD and diffuse Lewy body disease.
8 mice, brains of AR-JP and idiopathic PD and diffuse Lewy body disease also exhibit increased level o
9 as Lewy body variant of Alzheimer's disease, diffuse Lewy body disease, and Parkinson's disease and s
10 In Lewy body variant of Alzheimer's disease, diffuse Lewy body disease, and Parkinson's disease, NACP
11 arkinsonism, sporadic Parkinson disease, and diffuse Lewy Body disease as well as the 1-methyl-4-phen
13 comitant Alzheimer's/Parkinson's disease and diffuse Lewy body disease cases had significantly higher
14 rontotemporal degeneration (FTD) (n = 9), or diffuse Lewy body disease (DLB) with mixed AD or FTD pat
15 ological hallmark of Parkinson's disease and diffuse Lewy body disease (DLBD) is the aggregation of a
16 s isolated from postmortem human brains with diffuse Lewy body disease (DLBD) preferentially show end
18 7 Lewy body variant of AD [LBVAD] and 4 pure diffuse Lewy body disease [DLBD]) who had antemortem pos
22 omitant Alzheimer's/Parkinson's disease, and diffuse Lewy body disease) using in situ end labeling to
23 ilon4 allele in AD subjects with concomitant diffuse Lewy body disease was intermediate between contr
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