Serum response factor modulates neuron survival during peripheral axon injury. (57/71)

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Dissecting the effects of endogenous brain IL-2 and normal versus autoreactive T lymphocytes on microglial responsiveness and T cell trafficking in response to axonal injury. (58/71)

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Use of triple-convergence polypropylene thread for the aesthetic correction of partial facial paralysis caused by the facial nerve injury. (59/71)

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Simultaneous top-down modulation of the primary somatosensory cortex and thalamic nuclei during active tactile discrimination. (60/71)

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A system for delivering mechanical stimulation and robot-assisted therapy to the rat whisker pad during facial nerve regeneration. (61/71)

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Mesenchymal bone marrow stem cells within polyglycolic acid tube observed in vivo after six weeks enhance facial nerve regeneration. (62/71)

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Facial nerve grafting and end-to-end anastomosis in the middle ear: tympanic cavity and mastoid. (63/71)

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Evaluation of proximal facial nerve conduction by transcranial magnetic stimulation. (64/71)

A magnetic stimulator was used for direct transcutaneous stimulation of the intracranial portion of the facial nerve in 15 normal subjects and in patients with Bell's palsy, demyelinating neuropathy, traumatic facial palsy and pontine glioma. Compound muscle action potentials (CMAPs) thus elicited in the orbicularis oris muscle of controls were of similar amplitude but longer latency (1.3 SD 0.15 ms) compared with CMAPs produced by conventional electrical stimulation at the stylomastoid foramen. No response to magnetic stimulation could be recorded from the affected side in 15 of 16 patients with Bell's palsy. Serial studies in two patients demonstrated that the facial nerve remained inexcitable by magnetic stimulation despite marked improvement in clinical function. In the patient with a pontine glioma, the CMAP elicited by transcranial magnetic stimulation was of low amplitude but normal latency. In six of seven patients with demyelinating neuropathy, the response to intracranial magnetic stimulation was significantly delayed. Magnetic stimulation produced no response in either patient with traumatic facial palsy. Although the precise site of facial nerve stimulation is uncertain, evidence points to the labyrinthine segment of the facial canal as the most likely location.  (+info)