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1 diabetic peripheral neuropathy (DPN) of the tibial nerve.
2 cause macrophage infiltration of the distal tibial nerve.
3 conducted via electrical stimulation of the tibial nerve.
4 nd TA and stimulating cuffs on the posterior tibial nerve.
5 y reduced after capsaicin application on the tibial nerve.
6 APs of C-fibers could not be detected in the tibial nerve.
7 l sciatic nerve, mid-tibial nerve and distal tibial nerve.
8 , and demonstrates high expression levels in tibial nerve.
9 m/s) measured either in vivo or in isolated tibial nerves.
10 after stimulating ulnar, median, fibular and tibial nerves.
13 how morphological differences in the sciatic tibial nerve after 5 months of hyperglycemia when compar
17 interosseus muscles after stimulation of the tibial nerve and the low-frequency-dependent depression
18 ctrical stimulation was applied to the right tibial nerve, and standardized low-resolution brain elec
21 by applying an electrical stimulation to the tibial nerve as adolescents (Age = 14.8 +/- 2.5 yrs.) an
22 ciatic nerve at the sciatic notch and of the tibial nerve at the ankle were significantly reduced in
24 e at the middle level of the thigh or on the tibial nerve at the lower level of the lower hindlimb al
25 otential evoked calcium signals in mammalian tibial nerve axons using an in vitro mouse model with a
27 and lower limb mechanics with and without a tibial nerve block that prevented contraction of these m
28 rgery to treat foot drop entails rerouting a tibial nerve branch to the denervated common fibular ner
29 g, stimulation of the central end of the cut tibial nerve, brief repeated carotid occlusions and caro
31 Negative correlations were found for the tibial nerve conduction velocity (r = -0.23; 95% CI: -0.
32 Negative correlations were found for the tibial nerve conduction velocity (r = -0.24; 95% CI: -0.
34 Topical application of capsaicin (1%) on the tibial nerve did not affect SCS-induced vasodilation at
36 ele at this locus was associated with higher tibial nerve expression of an adjacent gene (SCN2A) codi
39 e injury by direct electrical stimulation of tibial nerve fibres, confirming that centrally mediated
41 beta, mRNA expression in the rat sciatic and tibial nerves following ischemia-reperfusion (IR) injury
42 ment transport in mature myelinated axons of tibial nerves from male and female mice of this strain e
43 ed by applying electrical stimulation to the tibial nerve in 22 persons with CP and 25 neurotypical c
45 The reflex was evoked by stimulating the tibial nerve in decerebrated rats whose femoral artery w
46 ibular nerve crush, CES was delivered to the tibial nerve in half the animals, and at 2 weeks, all an
48 cle contraction evoked by stimulation of the tibial nerve increased mean arterial pressure (MAP) and
52 easurements included peroneal nerve skin and tibial nerve muscle sympathetic activities; the electroc
53 r, combined interventions improved sural and tibial nerve myelin thickness, hind paw epidermal innerv
55 nduction velocity deficits, and reduction in tibial nerve myelinated fiber diameter, but not intraepi
57 nificant cis-eQTLs for PMF1 (P = 1 x 10-4 in tibial nerve), NBEAL1, FAM117B and CARF (P < 2.1 x 10-7
58 covered proximal (sciatic nerve) and distal (tibial nerve) nerve segments of the lower extremity.
59 eceptive properties of regenerated cutaneous tibial nerve nociceptors, and to obtain evidence for cou
63 ach of the supplying arteries to the sciatic-tibial nerves of the right hind limb was ligated and the
64 rats the effects of ligating and cutting one tibial nerve on sensory function and on density of inner
66 ) amplitudes of median, ulnar, peroneal, and tibial nerves (P < 0.001), but was not related to cortic
67 nally, iPSCMNs grafted into transected mouse tibial nerve projected axons to denervated gastrocnemius
68 scle action potentials ratio of peroneal and tibial nerves (split index, SI) and semi-quantitative sc
70 ssess the long-term efficacy of percutaneous tibial nerve stimulation (PTNS) in fecal incontinence (F
74 e of sacral neuromodulation and percutaneous tibial nerve stimulation in the treatment of men with ur
76 Both sacral neuromodulation and percutaneous tibial nerve stimulation prove to be viable, durable opt
77 ight-sided (i) handgrip; and (ii) median and tibial nerve stimulation were assessed using functional
78 eal nerve; test reflex elicited by posterior tibial nerve stimulation) was used during: (1) rest, (2)
79 l injection of botulinum toxin, percutaneous tibial nerve stimulation, sacral neuromodulation, and su
80 (MAP) and heart rate (HR) following a 2-min tibial nerve stimulation-evoked static muscle contractio
85 the femoral, common peroneal, and posterior tibial nerves (targeting the quadriceps femoris, tibiali
86 n, Merkel cells are lost from the denervated tibial nerve territory but are relatively preserved in n
87 g initial loss of cutaneous afferents in the tibial nerve territory, we observed progressive centripe
88 ernodal length (0.95-1.3 mm) in axons of the tibial nerve that varied in proportion to the mechanical
90 ese possibilities in rats after crushing the tibial nerve (TN), and using Vesicular GLUtamate Transpo
91 data from skeletal muscle, whole blood, and tibial nerve to test the effects of disease-associated p
95 emained at rest for the entire study, or the tibial nerve was stimulated, as in the contraction group
100 s, a stimulus was delivered to the posterior tibial nerve while the ipsilateral leg was moving either
101 in the rat, C nociceptors isolated from the tibial nerve with receptive fields (RFs) on the plantar