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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
7 , compound muscle action potentials ratio of peroneal and tibial nerves (split index, SI) and semi-qu
8 ves innervating both skin and muscle (common peroneal and tibial) or just muscle (lateral/medial gast
10 lectrical stimulation of the femoral, common peroneal, and posterior tibial nerves (targeting the qua
11 otential (CMAP) amplitudes of median, ulnar, peroneal, and tibial nerves (P < 0.001), but was not rel
14 o a cutaneous nerve, usually the superficial peroneal close to the ankle, and intraneural microstimul
15 re subject to fasciotomy of the anterior and peroneal compartment using a dual-incision minimally inv
16 ve fasciotomy to decompress the anterior and peroneal compartments of the lower leg appears to be saf
19 jor arteries (anterior and posterior tibial, peroneal), demarcation of origin of major arteries, and
20 ressive skeletal muscle weakness in a humero-peroneal distribution, early contractures and prominent
22 ts, eNG, and rNG all had similar patterns of peroneal functional index improvement after implantation
24 01) in femoral, popliteal, posterior tibial, peroneal, gastrocnemial, and soleal veins; reflux was di
25 vein (anterior tibial, posterior tibial, or peroneal) in 243 patients (63.2%) and a muscular branch
27 y (MSNA) was measured during wakefulness via peroneal microneurography in seven patients with documen
31 red muscle sympathetic nerve activity (MSNA, peroneal microneurography) in 5 healthy humans under con
33 l of sympathetic activity by measuring MSNA (peroneal microneurography), arterial pressure (arterial
36 tested, elevated triglycerides and decreased peroneal motor NCV at baseline significantly correlated
37 001), IENFD (p = 0.04), sural (p = 0.02) and peroneal motor nerve conduction velocity (p = 0.03) dete
39 nent of the plantar aponeurosis (PAL), short peroneal muscle (SPM) tendon, and third peroneal muscle
41 uced by afferents of the quadriceps and deep peroneal muscle nerves (which discharged 70-80% of extra
49 ex was conditioned by stimulating the common peroneal nerve (CPN) at short (2, 3, and 4 ms) and long
51 sion of the soleus H-reflex evoked by common peroneal nerve (CPN) stimulation, D1 inhibition] and het
52 rupt cutaneous feedback from the superficial peroneal nerve (foot dorsum) and medial plantar nerve (f
53 ded muscle sympathetic nerve activity in the peroneal nerve (intraneural electrodes) and the ECG (sur
54 amplitude of the ulnar nerve (p=0.0103) and peroneal nerve (p<0.0001), compared with baseline, were
56 neuropathy symptom profile, lower sural and peroneal nerve amplitudes, abnormal thermal thresholds,
58 rat dorsiflexors (n = 46) by activating the peroneal nerve and plantarflexing the foot ~40 deg, corr
59 We assessed SSNA (microneurography) from the peroneal nerve and skin blood flow (forearm laser Dopple
60 y 150 msec), and combined stimulation of the peroneal nerve and the motor cortex with transcranial ma
61 th stimulating electrodes on the left common peroneal nerve and with electromyographic (EMG) electrod
62 unilaterally stimulated via the right common peroneal nerve at 10 Hz and supramaximal voltage for 8 h
63 15+ cells correlated with NCVs of motor deep peroneal nerve at 2 years post-gene therapy, and ARSA le
64 eolus, just before stimulation of the common peroneal nerve at the head of the fibula, decreased the
65 by electrically stimulating the superficial peroneal nerve bilaterally, before and after staggered l
66 mpathetic nerve activity was measured in the peroneal nerve by microneurography, and the slope of the
68 mporally dependent PAS applied to the common peroneal nerve during the swing phase of walking would i
69 n lower limb motor cortex paired with common peroneal nerve electrical stimulation produces a lasting
70 chronically and to stimulate the superficial peroneal nerve electrically to evoke cutaneous reflexes.
71 lied at ST36-37 acupoints overlying the deep peroneal nerve for 30 min twice weekly for five weeks wh
73 oots were cut flush to the spinal cord and a peroneal nerve graft was inserted into the lateral spina
74 Continuous unilateral stimulation of the peroneal nerve in rats for 8 h per day for 2 or 7 days c
76 sympathetic nerve fibres of the superficial peroneal nerve innervating the dorsum of the foot were r
78 toplethysmographic finger arterial pressure, peroneal nerve muscle sympathetic activity and plasma no
79 inger arterial pressures and in 15 patients, peroneal nerve muscle sympathetic activity before and du
80 mographic arterial pressure, respiration and peroneal nerve muscle sympathetic activity in four healt
81 mographic arterial pressure, respiration and peroneal nerve muscle sympathetic activity in nine healt
82 rbon dioxide concentrations and volumes, and peroneal nerve muscle sympathetic activity on Earth (in
85 erve activity to muscle circulation from the peroneal nerve of 12 chronic heart failure patients whil
88 on of cutaneous afferents in the superficial peroneal nerve on the locomotor discharges of single med
91 cles was assessed before and after 30 min of peroneal nerve stimulation at motor threshold intensity.
94 l patients underwent microneurography of the peroneal nerve to compare the sympathomimetic effects du
95 ted in an surgically created gap in the host peroneal nerve to evaluate their regeneration supporting
96 anglionic section of dorsal roots L4-L6, the peroneal nerve was stimulated (10 Hz, 8 h day(-1)) for 2
99 ty (MSNA) with intraneural electrodes in the peroneal nerve while the subject inspired (primarily wit
100 We measured MSNA (microneurography of the peroneal nerve) and forearm blood flow (FBF, Doppler ult
101 sculature using intraneural microelectrodes (peroneal nerve) during intranasal cocaine (2 mg/kg, n =
104 MSNA was measured by microneurography at the peroneal nerve, and arterial blood pressure, electrocard
105 e sciatic nerve and its branches such as the peroneal nerve, the tibial nerve, and the sural nerve.
106 imulation of group I afferents in the common peroneal nerve, was assessed from changes in the H refle
107 etrodotoxin (TTX)-administered to the common peroneal nerve-resulted in reductions in muscle mass of
112 (conditioned stimulus applied to the common peroneal nerve; test reflex elicited by posterior tibial
113 cally stimulating left and right superficial peroneal nerves before and after two thoracic lateral he
114 Group II afferents of quadriceps and deep peroneal nerves evoked potentials mainly at the rostral
116 nduction velocity for the median, ulnar, and peroneal nerves was decreased in patients with high vers
117 (brachial plexus, ulnar, femoral, and common peroneal nerves) for biceps brachii, first dorsal intero
122 rse peripheral nerves-occipital, vagus, deep peroneal, sciatic, tibial, and common peroneal nerves-fo
125 mputed tomographic data for the diagnosis of peroneal tendon subluxation or dislocation by using the
128 d consider all soft tissue structures (i.e., peroneal tendons, ligaments of the ankle, subtalar joint
130 ctional nerve conduction study analyzing the peroneal, tibial, median motor, and median sensory nerve
131 size of the muscle and the dimensions of the peroneal tubercle and retrotrochlear eminence were recor
132 easured the width, length, and height of the peroneal tubercle in 100 asymptomatic patients, comparin
133 ngs show that ultrasound measurements of the peroneal tubercle were consistent with values reported i
134 d imaging as a promising tool to measure the peroneal tubercle, and it could contribute to a better u
139 ts (age, 32+/-2 years; mean+/-s.e.m.), MSNA (peroneal) was assessed using standard microneurographic