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1 onitor spinal cerebrospinal fluid signal and motor evoked potentials).
2 al muscle twitch can be produced, called the motor-evoked potential.
3 ike) of cortical excitability as measured by motor evoked potentials.
4 on and assessed using a limb motor score and motor-evoked potentials.
5 in cortical excitability were assessed using motor-evoked potentials.
7 in intracortical facilitation (P < .01) and motor-evoked potential amplitude (P < .05) as well as a
14 eus), as shown by increased amplitude of the motor evoked potentials and decreased duration of the co
15 ntensity to elicit a predefined amplitude of motor-evoked potential and EEG theta activity) and decre
16 F-OPC grafts recovered transcranial magnetic motor-evoked potential and magnetic interenlargement ref
17 ed associative stimulation induced change in motor-evoked potential and memory formation) after sleep
18 icians, vibration increases the amplitude of motor-evoked potentials and decreases the short-latency
19 ning-dependent increases in the amplitude of motor-evoked potentials and motor map reorganization are
21 with primary lateral sclerosis had abnormal motor-evoked potentials as assessed using transcranial m
23 ance deteriorates and both somatosensory and motor evoked potentials decrease over contralateral sens
25 elivered to the C3-C5 level on (1) diaphragm motor-evoked potentials (DiMEPs) elicited by transcrania
30 n cognitive context: pre-SMA facilitated the motor evoked-potential elicited by M1 stimulation only d
32 rent inhibition was measured by conditioning motor evoked potentials, elicited by transcranial magnet
33 r activation, comparable to the monosynaptic motor-evoked potential evoked by TMS of primary motor co
34 rimary motor cortex, we examined ipsilateral motor-evoked potentials (iMEPs) in a proximal arm muscle
36 ural excitability were assessed by measuring motor-evoked potentials in a small hand muscle before an
37 transection, 70% of OEG-treated rats showed motor-evoked potentials in hindlimb muscles after transc
38 ion significantly increased the amplitude of motor-evoked potentials in individuals with the SNP that
39 wo independent assays and recorded hind-limb motor-evoked potentials in infected class I-deficient an
40 ility was tested by measuring recruitment of motor-evoked-potentials "input-output (IO) curve" and of
41 rotocols to evaluate motor excitability with motor-evoked potentials, input-output (IOcurve) and shor
44 netic stimulation of the motor cortex on the motor evoked potential (MEP) from transcranial magnetic
45 hemispheric) before acquisition of baseline motor evoked potential (MEP) recordings from each site a
46 ered at a subthreshold intensity to elicit a motor evoked potential (MEP), on the MEP response to an
47 ed with TMS, measuring motor threshold (MT), motor evoked-potential (MEP) size, and intracortical inh
48 hreshold, a greater proportional increase in motor-evoked potential (MEP) amplitude with voluntary fa
52 the first stimulus (S1) was set to produce a motor-evoked potential (MEP) of 1 mV in the resting cont
54 rug application, INB plus rTMS increased the motor-evoked potential (MEP) size and decreased intracor
55 Whereas controls showed inhibition of APB motor-evoked potential (MEP) size during movement initia
56 entify EAE31, a locus controlling latency of motor evoked potentials (MEPs) and clinical onset of exp
58 nd cervicomedullary stimulation, we examined motor evoked potentials (MEPs) and the activity in intra
60 representations during response preparation, motor evoked potentials (MEPs) elicited by transcranial
61 rtex (PMd) (CS2) suppresses the amplitude of motor evoked potentials (MEPs) from a test pulse (TS) ov
62 otor conduction times, normal thresholds for motor evoked potentials (MEPs) in leg muscles, and a nor
63 , or during the left limb movement to obtain motor evoked potentials (MEPs) in the muscles of the rig
67 tudies measuring the threshold for eliciting motor evoked potentials (MEPs) to transcranial magnetic
69 and the dorsal cervical spinal cord in rats; motor evoked potentials (MEPs) were measured from biceps
71 In addition, Hoffman reflex (H-reflex) and motor evoked potentials (MEPs) were recorded from the ga
74 creases cortical excitability as measured by motor-evoked potentials (MEPs) and (2) alters functional
75 eral nerve stimulation we examined in humans motor-evoked potentials (MEPs) and the activity in intra
77 lity were traced by simultaneously recording motor-evoked potentials (MEPs) and TMS-evoked EEG potent
78 ing the effect of ulnar nerve stimulation on motor-evoked potentials (MEPs) elicited by transcranial
79 10% resting motor threshold (RMT) suppressed motor-evoked potentials (MEPs) evoked in the first dorsa
80 y volunteers in two experiments, we measured motor-evoked potentials (MEPs) from TMS of the motor cor
81 ested this hypothesis in humans by measuring motor-evoked potentials (MEPs) in a left finger muscle d
82 asure corticospinal excitability by means of motor-evoked potentials (MEPs) in both the hand and the
83 pulse TMS at a specific interval facilitates motor-evoked potentials (MEPs) in hand muscles in a mann
85 spinal excitability and RT, such that larger motor-evoked potentials (MEPs) measured at rest were ass
86 .8 in the BBB scale), decreased amplitude of motor-evoked potentials (MEPs) recorded on tibialis ante
88 ranial magnetic stimulation (TMS) to measure motor-evoked potentials (MEPs) together with recruitment
91 A paired-pulse protocol was used, in which motor-evoked potentials (MEPs) were produced by cortical
92 transcranial magnetic stimulation (TMS), 25 motor-evoked potentials (MEPs) were recorded before, and
94 , with input from one hand muscle increasing motor-evoked potentials (MEPs), decreasing short and inc
96 review was conducted to examine the role of motor-evoked potential monitoring in spine and central n
98 threshold, the intensity needed to produce a motor evoked potential of 0.5 mV, and the amplitude of t
100 al changes in descending motor pathways with motor-evoked potentials recorded during cooling, we repo
101 pressure, we could increase the amplitude of motor-evoked potentials recorded from below or just abov
102 Our results show that the amplitude of the motor-evoked potentials recorded from the real hand is s
104 of D15A-GRPs recovered transcranial magnetic motor-evoked potential responses, indicating that conduc
105 duced (38%; SD +/- 7; P = 0.01) and the post-motor evoked potential silent period (101 ms; SEM +/- 10
107 short-term enhancement of cortico-pharyngeal motor evoked potentials, suggesting the feasibility of a
108 and grid walking] and transcranial magnetic motor-evoked potentials (tcMMEP) were studied at 1, 2, a
109 Corticospinal excitability was measured with motor-evoked potentials under transcranial magnetic stim
116 physiological effects (change in heart rate, motor evoked potentials) were observed during any of the
117 -pulse transcranial magnetic stimulation and motor-evoked potentials while healthy humans watched vid
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