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1 ICN was performed using a sural nerve graft.
2 reatment is surgery, requiring an autologous nerve graft.
3 ction, regardless of the BDNF content of the nerve graft.
4 ding to the development of the bioartificial nerve graft.
5 nd the great auricular nerve (GAN) as a free nerve graft.
6 o the permissive environment of a peripheral nerve graft.
7 to the clinical standard of care, autologous nerve grafts.
8 rve conduits as an alternative to autologous nerve grafts.
9 -promoting properties of freeze-killed donor nerve grafts.
10 can extend for long distances in peripheral nerve grafts.
11 reported poor permeability of freeze-thawed nerve grafts.
12 ficantly reduced in the 12-month degenerated nerve grafts.
13 nerative potential of normal and degenerated nerve grafts.
14 /-) axons robustly grew into mouse wild-type nerve grafts.
15 ned with their low immunogenicity, acellular nerve grafts activated by in vitro predegeneration may b
18 nsity of ascending axons growing through the nerve graft and scar tissue present at the rostral spina
21 r grafts and, compared with normal acellular nerve grafts, axonal ingress in vivo was approximately d
24 ve spinal cord injury, we built a peripheral nerve graft bridge (PNG) through the cystic cavity and t
25 XTas near the rostral border of a peripheral nerve graft bridging the transected dorsal columns in th
27 of axial cryosections of human cross-facial nerve grafts demonstrated enhanced resolution of small-c
29 into the dorsal column, 3 mm rostral to the nerve graft, essentially no fibers had extended from the
30 xus allotransplantation could offer the best nerve graft fulfilling the like-with-like principle.
32 nd extent of regeneration, the bioartificial nerve graft holds great promise for improving recovery i
33 ation of Purkinje cell axons into peripheral nerve grafts implanted into the cerebellum was examined.
34 nal axon outgrowth into implanted peripheral nerve grafts in a rat model of brachial plexus avulsion,
35 transplanted a growth supporting peripheral nerve graft into the lesion cavity, and enzymatically mo
36 red regeneration through OPN(-/-) peripheral nerves grafted into OPN(+/+) mice indicated that loss of
39 factor expression between sensory and motor nerve, grafts of cutaneous nerve or ventral root were de
40 Nerve gaps were bridged by either a sural nerve graft or a biodegradable collagen nerve guide tube
41 l cord provided with a permissive peripheral nerve graft (PNG) as well as in crushed optic nerve.
42 ), alone or in conjunction with a peripheral nerve graft (PNG), to alter the molecular program of inj
44 regenerate into growth-permissive peripheral nerve grafts (PNGs) reenter host tissue to mediate funct
47 ur studies provide evidence that an enhanced nerve grafting strategy represents a potential regenerat
48 sent study, we modified a classic peripheral nerve grafting technique with the use of chondroitinase
50 onths after nerve sprouting was induced by a nerve graft, the same NMJs were restained and reexamined
53 mammals or regenerate axons into peripheral nerve grafts to test the importance of these molecules f
54 d regeneration nerve fibers through CLU(-/-) nerve grafts transplanted into CLU(+/+) mice indicated t
55 ated their axons through a 1.5 cm peripheral nerve graft twofold relative to uninjected controls and
56 e developed a method for preparing cell-free nerve grafts using lysophosphatidylcholine to remove cel
58 cut flush to the spinal cord and a peroneal nerve graft was inserted into the lateral spinal cord at
59 of sensory fibers in the rostral end of the nerve graft was not significantly different between cont
61 achieved with minimal morbidity using sural nerve grafts, which surgeons commonly use to reconstruct
62 ected optic nerve after intravitreal sciatic nerve grafting without inhibitory ligand neutralization.