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1 rons also innervate motoneurons of intrinsic hand muscles.
2 ect cortico-motoneuronal (CM) connections to hand muscles.
3 d projects to spinal motoneurons controlling hand muscles.
4 seen across motor nuclei supplying extrinsic hand muscles.
5 d 16 years, followed by atrophy of intrinsic hand muscles.
6 t was suppressed during contraction of right hand muscles.
7 occipital cortex evoked contraction of right hand muscles.
8 Responses were recorded from two intrinsic hand muscles.
9 ving the opposite effect on the non-vibrated hand muscles.
10 ing the primary motor cortex (M1) outputs to hand muscles.
11 roprioceptive feedback in the control of the hand muscles.
12 steady contractions of contralateral arm and hand muscles.
13 led to evoke ipsilateral responses in arm or hand muscles.
14 pools innervating homologous left and right hand muscles.
15 on (pdTES), in both preactivated and relaxed hand muscles.
16 ) coherence with electromyogram from a right hand muscle; 2) a typical sensorimotor Mu rhythm at rest
20 During grasp there was a specific pattern of hand muscle activity according to the object grasped.
21 project to spinal motor neurons controlling hand muscles and extensively sprout into gray matter str
22 low amplitude vibration to single intrinsic hand muscles and measuring motor cortex excitability wit
24 ectromyograms (EMGs) were recorded from four hand muscles, and reflexes were averaged during each tas
25 ns, we tested the hypothesis that aspects of hand muscle architecture that are known to be influenced
28 e short latency Hoffmann reflex to a treated hand muscle as well as low threshold polysynaptic spinal
31 rticomuscular conduction delay for intrinsic hand muscles calculated from the phase-frequency regress
32 n of vibration applied simultaneously to two hand muscles can lead to long-term (> 30 min) changes in
35 spinal motoneurons (F-waves) in an intrinsic hand muscle during index finger abduction, precision gri
39 trast, the modulation of reflex responses of hand muscles during rhythmic movement is poorly document
40 Electromyographic recordings of neck and hand muscles during scanning ensured compliance with the
41 ion grip, coherence between motor cortex and hand muscle EMG oscillatory activity in the 15-30 Hz ran
42 motor units were identified in an intrinsic hand muscle (first dorsal interosseous, FDI) or an axial
43 in turn to each of three different intrinsic hand muscles (first dorsal interosseus, FDI; abductor po
44 Motor-evoked potentials were recorded from a hand muscle in 12 patients with PD (7 patients were test
45 ork output in contractions of a single human hand muscle in vivo and of the ATP cost of that work to
47 acilitates motor-evoked potentials (MEPs) in hand muscles in a manner that varies with the role of th
48 ver, while there was broad excitation in the hand muscles in Go trials, suppression in NoGo trials wa
49 sorimotor EEGs and EMGs from three intrinsic hand muscles in human subjects performing a precision gr
50 in the size of the representation of paretic hand muscles in the ipsilesional motor cortex after CIMT
51 on in the hand is focal, with input from one hand muscle increasing motor-evoked potentials (MEPs), d
53 ility in WC, it strongly reduced SICI in all hand muscles irrespective of spatial organization in MD.
55 ory influence of the human M1 on ipsilateral hand muscles is to a significant extent mediated below t
56 ons innervating forearm flexor and intrinsic hand muscles, not in forearm extensor motor neurons.
57 nction scores, electromyography from arm and hand muscles, placebo-expectancy effects, and functional
58 core of distal (wrist, digit, and intrinsic hand) muscle representation surrounded by a "horseshoe"-
59 ) to modulate motor responses in ipsilateral hand muscles seems to be important for normal motor cont
60 8 % of control) and more in the non-vibrated hand muscles (test response reduced to 27 +/- 5 % of con
61 17 +/- 3 % control) than in the non-vibrated hand muscles (test response reduced to 80 +/- 11 % contr
63 ticospinal outputs to the vibrated and other hand muscles was evaluated with transcranial magnetic st
64 amplitudes and motor output curves in small hand muscles were depressed and motor thresholds were el
66 subcortical pathways targeting an intrinsic hand muscle when grasping a small (6 mm) cylinder betwee
67 nd spinal motoneurons (F-waves) in intrinsic hand muscles when grasping a 6 mm cylinder with the inde
68 urons, and motor neurons supplying intrinsic hand muscles, which all play important roles in mediatin
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