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1 f individual fascicles (tibial, peroneal and sural).
2 of myelinated and unmyelinated axons in the sural and medial plantar nerves that immunostain for sub
3 d a higher neuropathy symptom profile, lower sural and peroneal nerve amplitudes, abnormal thermal th
5 gical assessment (Total Neuropathy Score and sural and tibial compound nerve amplitudes), and sensory
6 Moreover, combined interventions improved sural and tibial nerve myelin thickness, hind paw epider
8 by random regeneration in direct suture and sural cable graft groups but not in nerve guide repairs
12 staining of lateral plantar nerve (LPN) and sural nerve (SN) motor terminals, using the activity-dep
13 nd the F-wave latency (p=0.03) decreased and sural nerve action potential amplitude increased (p=0.04
14 Changes in excitability of the terminals of sural nerve afferents were used to confirm that both loc
15 ith BIPN more frequently demonstrated absent sural nerve amplitudes and diminished distal sensation c
17 ical stimulation of afferent C fibers in the sural nerve and recorded from single neurons in the vent
20 was evoked by electrical stimulation of the sural nerve and was recorded in the ipsilateral hamstrin
21 vestigated the surgical anatomy of the ovine sural nerve as a potential candidate for facial nerve re
25 ibres was a uniform feature in a total of 21 sural nerve biopsies and 'onion bulb' formations and/or
26 ith diabetic neuropathy progression in human sural nerve biopsies and describe their potential utilit
29 -4 (CD152) at the protein and mRNA levels in sural nerve biopsies of patients with chronic inflammato
30 eased PMP22 messenger RNA levels in skin and sural nerve biopsies of patients with CMT1A compared wit
31 and nuclear imaging, electroencephalography, sural nerve biopsies, sleep evaluation and neuropsychome
36 lectrophysiologic data were evaluated, and a sural nerve biopsy from one affected child was examined
37 tain circumstances replace the more invasive sural nerve biopsy in the morphological and molecular ev
43 area of the antidromic volley evoked in the sural nerve by intraspinal microstimulation in the L4/5
44 unmyelinated fiber function in the hind paw, sural nerve C-fiber morphometry, sciatic nerve neurotrop
48 Nociceptive nerve function, unmyelinated sural nerve fiber and dorsal root ganglion (DRG) cell mo
52 can be achieved with minimal morbidity using sural nerve grafts, which surgeons commonly use to recon
65 Stimulation of the gastrocnemius nerve and sural nerve revealed significant convergence of muscle a
75 The mean number of myelinated fibers in the sural nerve was significantly lower than that of the BB
76 were exposed and in situ recordings from the sural nerve were performed to determine compound C-fiber
78 omy and the number of fascicles of the ovine sural nerve were similar of those reported in humans.
80 lation of a 54-kDa isoform of JNK in DRG and sural nerve, and this correlated with elevated c-Jun and
90 pathies and compared these with normal human sural nerves and those from patients with Guillain-Barre
91 iments were performed on 50 samples of human sural nerves collected during a 52-week clinical trial.
93 urofilament distances (NNND) in the axons of sural nerves from patients with anti-MAG paraproteinaemi
94 e sensory latency of both the left and right sural nerves improved on the basis of faster median cond
95 f HIV-SN, freshly isolated mitochondria from sural nerves of macaques infected with a neurovirulent s
96 mtDNA common deletion mutation in postmortem sural nerves of patients with HIV-SN as compared to unin
97 s from four cryopreserved normal adult human sural nerves referenced to the Genome Reference Consorti
98 icantly lower C-fiber conduction velocity in sural nerves than uninfected animals and the magnitude o
103 and to monitor long-term outcomes, with the sural or dorsal sural nerve as the most informative.
105 large myelinated nerve fibers, specifically sural or sciatic nerve conduction velocities, but signif
106 .0001), CNFL (p < 0.0001), IENFD (p = 0.04), sural (p = 0.02) and peroneal motor nerve conduction vel
107 nerve conduction studies (NCS), specifically sural sensory nerve action potential (SNAP) amplitude, w
109 oral dispersion and conduction block, (5) no sural sparing, (6) greater number of fibrillation potent