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1 l sweat rate and SSNA (microneurography from peroneal nerve).
2 leus H-reflex with stimulation of the common peroneal nerve.
3 ltaneous stimulation of the hypothalamus and peroneal nerve.
4 in the hypothalamus and in the isolated left peroneal nerve.
5  truncations and deletions of the tibial and peroneal nerves.
6          Morphometric analysis of the distal peroneal nerve and extensor digitorum muscle weight were
7  rat dorsiflexors (n = 46) by activating the peroneal nerve and plantarflexing the foot ~40 deg, corr
8 We assessed SSNA (microneurography) from the peroneal nerve and skin blood flow (forearm laser Dopple
9 y 150 msec), and combined stimulation of the peroneal nerve and the motor cortex with transcranial ma
10 th stimulating electrodes on the left common peroneal nerve and with electromyographic (EMG) electrod
11    We measured MSNA (microneurography of the peroneal nerve) and forearm blood flow (FBF, Doppler ult
12 MSNA was measured by microneurography at the peroneal nerve, and arterial blood pressure, electrocard
13 unilaterally stimulated via the right common peroneal nerve at 10 Hz and supramaximal voltage for 8 h
14 eolus, just before stimulation of the common peroneal nerve at the head of the fibula, decreased the
15 mpathetic nerve activity was measured in the peroneal nerve by microneurography, and the slope of the
16           People with severe PAD have poorer peroneal nerve conduction velocity compared with people
17 ex was conditioned by stimulating the common peroneal nerve (CPN) at short (2, 3, and 4 ms) and long
18                                       Common peroneal nerve (CPN) stimulation paired with transcrania
19 mporally dependent PAS applied to the common peroneal nerve during the swing phase of walking would i
20 sculature using intraneural microelectrodes (peroneal nerve) during intranasal cocaine (2 mg/kg, n =
21 n lower limb motor cortex paired with common peroneal nerve electrical stimulation produces a lasting
22 chronically and to stimulate the superficial peroneal nerve electrically to evoke cutaneous reflexes.
23    Group II afferents of quadriceps and deep peroneal nerves evoked potentials mainly at the rostral
24 rupt cutaneous feedback from the superficial peroneal nerve (foot dorsum) and medial plantar nerve (f
25 lied at ST36-37 acupoints overlying the deep peroneal nerve for 30 min twice weekly for five weeks wh
26                                              Peroneal nerve function was present in half the rats at
27 oots were cut flush to the spinal cord and a peroneal nerve graft was inserted into the lateral spina
28     Continuous unilateral stimulation of the peroneal nerve in rats for 8 h per day for 2 or 7 days c
29  sympathetic nerve fibres of the superficial peroneal nerve innervating the dorsum of the foot were r
30 ded muscle sympathetic nerve activity in the peroneal nerve (intraneural electrodes) and the ECG (sur
31       The primary endpoint was the change in peroneal nerve motor conduction velocity.
32 toplethysmographic finger arterial pressure, peroneal nerve muscle sympathetic activity and plasma no
33 inger arterial pressures and in 15 patients, peroneal nerve muscle sympathetic activity before and du
34 mographic arterial pressure, respiration and peroneal nerve muscle sympathetic activity in four healt
35 mographic arterial pressure, respiration and peroneal nerve muscle sympathetic activity in nine healt
36 rbon dioxide concentrations and volumes, and peroneal nerve muscle sympathetic activity on Earth (in
37 espiratory carbon dioxide concentrations and peroneal nerve muscle sympathetic activity.
38 tory carbon dioxide levels, tidal volume and peroneal nerve muscle sympathetic activity.
39 erve activity to muscle circulation from the peroneal nerve of 12 chronic heart failure patients whil
40                     Motoneuron perikarya and peroneal nerve of diabetic rats showed no evidence of in
41                                   The common peroneal nerve of Sprague-Dawley rats was transected and
42 isografts (15 mm long) were implanted in the peroneal nerves of F-344 rats.
43 on of cutaneous afferents in the superficial peroneal nerve on the locomotor discharges of single med
44  amplitude of the ulnar nerve (p=0.0103) and peroneal nerve (p<0.0001), compared with baseline, were
45                                       Common peroneal nerve palsy was present in two patients.
46 etrodotoxin (TTX)-administered to the common peroneal nerve-resulted in reductions in muscle mass of
47                        Measurements included peroneal nerve skin and tibial nerve muscle sympathetic
48 cles was assessed before and after 30 min of peroneal nerve stimulation at motor threshold intensity.
49 ls received either hypothalamic stimulation, peroneal nerve stimulation, or both.
50                These effects were reduced by peroneal nerve stimulation.
51  (conditioned stimulus applied to the common peroneal nerve; test reflex elicited by posterior tibial
52 e sciatic nerve and its branches such as the peroneal nerve, the tibial nerve, and the sural nerve.
53 l patients underwent microneurography of the peroneal nerve to compare the sympathomimetic effects du
54 ted in an surgically created gap in the host peroneal nerve to evaluate their regeneration supporting
55 anglionic section of dorsal roots L4-L6, the peroneal nerve was stimulated (10 Hz, 8 h day(-1)) for 2
56 nduction velocity for the median, ulnar, and peroneal nerves was decreased in patients with high vers
57 imulation of group I afferents in the common peroneal nerve, was assessed from changes in the H refle
58 d muscle sympathetic nerve activity from the peroneal nerve were recorded continuously.
59 ty (MSNA) with intraneural electrodes in the peroneal nerve while the subject inspired (primarily wit

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