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1 be good apomorphine antagonists but all were dyskinetic.
2 ts N-2-(2-hydroxyethoxy)ethyl analogue 3 was dyskinetic.
3 zepines, 2 was not dyskinetic whereas 2a was dyskinetic.
4 m and a reduction in SN of both unprimed and dyskinetic 6-hydroxydopamine rats, consistent with oppos
5 equency significantly increased in ON L-DOPA dyskinetic 6-hydroxydopamine-lesioned rats, suggesting t
6 lidum does not separate antiparkinsonian and dyskinetic actions implies that they are closely related
8 size (maximum dimension, 10 to 66 mm), were dyskinetic/akinetic with thin rims, and were associated
9 In the 'OFF' state withdrawn from levodopa, dyskinetic and non-dyskinetic patients had similar level
13 y contact(i.e., multisynaptic spines) in the dyskinetic animals compared with the 6-hydroxydopamine-t
15 between 15% and 40%, and dilated akinetic or dyskinetic anterior-apical wall without the need to be r
16 area r=-0.51, P<0.0001; RVOT displacement of dyskinetic area r=-0.49, P<0.0001; and RVOT late gadolin
17 VOT ejection fraction r=0.64, P<0.0001; RVOT dyskinetic area r=-0.51, P<0.0001; RVOT displacement of
18 l extent of dyskinetic area, displacement of dyskinetic area, and score of extent of late gadolinium
19 gmental ejection fraction, spatial extent of dyskinetic area, displacement of dyskinetic area, and sc
21 st, children with quadriplegic and mixed CP (dyskinetic, athetoid, hypotonic, and ataxic) more often
22 arcted segment is often akinetic rather than dyskinetic because early reperfusion prevents transmural
23 riatonigral medium spiny neurons exacerbated dyskinetic behavior, whereas overexpression of cJun, whi
24 and cocaine-induced locomotion and abolished dyskinetic behaviors in response to the Parkinson's dise
26 ndrites that appear to be directly linked to dyskinetic behaviors, since they were not seen in the st
34 normal airway epithelial cells had stiff and dyskinetic cilia beating patterns compared to control ce
36 at NMDA receptor blockade may ameliorate the dyskinetic complications of long-term levodopa therapy,
37 w, and comprised all infants with spastic or dyskinetic CP not caused by developmental abnormalities
38 children with moderate to severe spastic or dyskinetic CP not due to postnatal brain injury or devel
45 bjects with schizotypal personality had more dyskinetic-like movements than subjects with schizoid pe
48 of behavioral sensitization (an increase in dyskinetic-like movements), but spectrum subjects showed
50 -4-phenyl-1,2,3,6-tetrahydropyridine-treated dyskinetic macaques without affecting the global parkins
51 this normalization of basal excitability, in dyskinetic mice, the selective D1R agonist SKF38393 incr
52 Hb was found to be metabolically modified in dyskinetic monkeys and its neuronal firing frequency sig
56 ent displaying a disorder characterized by a dyskinetic movement disorder, developmental delay, and a
57 g this variant presented with an early onset dyskinetic movement disorder, severe motor delay, and pr
59 kinesia, as seen in Parkinson's disease, and dyskinetic movements as seen in Huntington's disease or
60 neurocircuitry hypothesized to give rise to dyskinetic movements has also been implicated in psychot
61 ine and l-dopa-induced normal ambulatory and dyskinetic movements in Pitx3 mutant mice, whereas the s
62 ggested to underlie dopamine-agonist-induced dyskinetic movements that develop during the treatment o
68 oxysmal episodes in puberty, either dystonic/dyskinetic or "shivering" attacks, triggered by stretchi
70 of left ventricular (LV) reconstruction for dyskinetic or akinetic LV segments in patients with isch
72 ography was performed in the 'ON' condition, dyskinetic patients had higher (11)C-CNS 5161 uptake in
73 withdrawn from levodopa, dyskinetic and non-dyskinetic patients had similar levels of tracer uptake
74 atients without dyskinesias, suggesting that dyskinetic patients may have abnormal glutamatergic tran
77 ether the opioid system is involved in human dyskinetic PD, we measured in vivo opioid receptor bindi
79 e for a dramatic rewiring of the striatum of dyskinetic rats and that this rewiring involves corticos
80 s overexpressed only on the lesioned side of dyskinetic rats in LHb and co-localized with DeltaFosB,
82 ration response, long-duration response, and dyskinetic response to levodopa change during long-term
83 y raise the possibility that the maladaptive dyskinetic responses to chronic l-DOPA treatment in Park
84 PNs oppositely modulate both therapeutic and dyskinetic responses to dopamine replacement therapy in
85 mice, hM3Dq stimulation of dSPNs exacerbated dyskinetic responses to L-DOPA, while stimulation of iSP
86 of 360 segments), especially in akinetic and dyskinetic segments (276 [91%] of 303), irrespective of
93 or high myopia, absence of binocular fusion, dyskinetic strabismus, severe gaze dysfunction, and opti
96 ioning that might underlie the generation of dyskinetic symptoms in patients with PD who have receive
99 pectively, in segments that were akinetic or dyskinetic under resting conditions (83% concordance wit
101 6-hydroxydopamine lesions (6-OHDA) rendered dyskinetic with chronic L-DOPA treatment reveals a compl
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