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1 on velocities ranging from 7.5 to 27.0m/sec (peroneal).
3 was significantly higher in controls (tibial/peroneal: 82.0 +/- 2.1/78.3 +/- 1.7) versus MS (tibial/p
4 ves innervating both skin and muscle (common peroneal and tibial) or just muscle (lateral/medial gast
7 o a cutaneous nerve, usually the superficial peroneal close to the ankle, and intraneural microstimul
8 jor arteries (anterior and posterior tibial, peroneal), demarcation of origin of major arteries, and
9 ressive skeletal muscle weakness in a humero-peroneal distribution, early contractures and prominent
10 ts, eNG, and rNG all had similar patterns of peroneal functional index improvement after implantation
12 01) in femoral, popliteal, posterior tibial, peroneal, gastrocnemial, and soleal veins; reflux was di
13 vein (anterior tibial, posterior tibial, or peroneal) in 243 patients (63.2%) and a muscular branch
15 y (MSNA) was measured during wakefulness via peroneal microneurography in seven patients with documen
18 red muscle sympathetic nerve activity (MSNA, peroneal microneurography) in 5 healthy humans under con
20 l of sympathetic activity by measuring MSNA (peroneal microneurography), arterial pressure (arterial
22 tested, elevated triglycerides and decreased peroneal motor NCV at baseline significantly correlated
24 nent of the plantar aponeurosis (PAL), short peroneal muscle (SPM) tendon, and third peroneal muscle
26 uced by afferents of the quadriceps and deep peroneal muscle nerves (which discharged 70-80% of extra
33 ex was conditioned by stimulating the common peroneal nerve (CPN) at short (2, 3, and 4 ms) and long
35 rupt cutaneous feedback from the superficial peroneal nerve (foot dorsum) and medial plantar nerve (f
36 ded muscle sympathetic nerve activity in the peroneal nerve (intraneural electrodes) and the ECG (sur
37 amplitude of the ulnar nerve (p=0.0103) and peroneal nerve (p<0.0001), compared with baseline, were
39 rat dorsiflexors (n = 46) by activating the peroneal nerve and plantarflexing the foot ~40 deg, corr
40 We assessed SSNA (microneurography) from the peroneal nerve and skin blood flow (forearm laser Dopple
41 y 150 msec), and combined stimulation of the peroneal nerve and the motor cortex with transcranial ma
42 th stimulating electrodes on the left common peroneal nerve and with electromyographic (EMG) electrod
43 unilaterally stimulated via the right common peroneal nerve at 10 Hz and supramaximal voltage for 8 h
44 eolus, just before stimulation of the common peroneal nerve at the head of the fibula, decreased the
45 mpathetic nerve activity was measured in the peroneal nerve by microneurography, and the slope of the
47 mporally dependent PAS applied to the common peroneal nerve during the swing phase of walking would i
48 n lower limb motor cortex paired with common peroneal nerve electrical stimulation produces a lasting
49 chronically and to stimulate the superficial peroneal nerve electrically to evoke cutaneous reflexes.
50 lied at ST36-37 acupoints overlying the deep peroneal nerve for 30 min twice weekly for five weeks wh
52 oots were cut flush to the spinal cord and a peroneal nerve graft was inserted into the lateral spina
53 Continuous unilateral stimulation of the peroneal nerve in rats for 8 h per day for 2 or 7 days c
54 sympathetic nerve fibres of the superficial peroneal nerve innervating the dorsum of the foot were r
56 toplethysmographic finger arterial pressure, peroneal nerve muscle sympathetic activity and plasma no
57 inger arterial pressures and in 15 patients, peroneal nerve muscle sympathetic activity before and du
58 mographic arterial pressure, respiration and peroneal nerve muscle sympathetic activity in four healt
59 mographic arterial pressure, respiration and peroneal nerve muscle sympathetic activity in nine healt
60 rbon dioxide concentrations and volumes, and peroneal nerve muscle sympathetic activity on Earth (in
63 erve activity to muscle circulation from the peroneal nerve of 12 chronic heart failure patients whil
66 on of cutaneous afferents in the superficial peroneal nerve on the locomotor discharges of single med
69 cles was assessed before and after 30 min of peroneal nerve stimulation at motor threshold intensity.
72 l patients underwent microneurography of the peroneal nerve to compare the sympathomimetic effects du
73 ted in an surgically created gap in the host peroneal nerve to evaluate their regeneration supporting
74 anglionic section of dorsal roots L4-L6, the peroneal nerve was stimulated (10 Hz, 8 h day(-1)) for 2
76 ty (MSNA) with intraneural electrodes in the peroneal nerve while the subject inspired (primarily wit
77 We measured MSNA (microneurography of the peroneal nerve) and forearm blood flow (FBF, Doppler ult
78 sculature using intraneural microelectrodes (peroneal nerve) during intranasal cocaine (2 mg/kg, n =
80 MSNA was measured by microneurography at the peroneal nerve, and arterial blood pressure, electrocard
81 e sciatic nerve and its branches such as the peroneal nerve, the tibial nerve, and the sural nerve.
82 imulation of group I afferents in the common peroneal nerve, was assessed from changes in the H refle
83 etrodotoxin (TTX)-administered to the common peroneal nerve-resulted in reductions in muscle mass of
87 (conditioned stimulus applied to the common peroneal nerve; test reflex elicited by posterior tibial
88 Group II afferents of quadriceps and deep peroneal nerves evoked potentials mainly at the rostral
90 nduction velocity for the median, ulnar, and peroneal nerves was decreased in patients with high vers
94 mputed tomographic data for the diagnosis of peroneal tendon subluxation or dislocation by using the
97 d consider all soft tissue structures (i.e., peroneal tendons, ligaments of the ankle, subtalar joint
99 size of the muscle and the dimensions of the peroneal tubercle and retrotrochlear eminence were recor
102 ts (age, 32+/-2 years; mean+/-s.e.m.), MSNA (peroneal) was assessed using standard microneurographic
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