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10.1097/PRS.0b013e3181c2a5ea

http://scihub22266oqcxt.onion/10.1097/PRS.0b013e3181c2a5ea
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C4394362!4394362!20048604
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suck abstract from ncbi


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pmid20048604      Plast+Reconstr+Surg 2010 ; 125 (1): 99-109
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  • Rodent Facial Nerve Recovery After Selected Lesions and Repair Techniques #MMPMID20048604
  • Hadlock TA; Kowaleski J; Lo D; Mackinnon SE; Heaton JT
  • Plast Reconstr Surg 2010[Jan]; 125 (1): 99-109 PMID20048604show ga
  • Background: Measuring rodent facial movements is a reliable method for studying recovery from facial nerve manipulation, and for examining the behavioral correlates of aberrant regeneration. We quantitatively compared recovery of vibrissal and ocular function following three types of clinically relevant nerve injury. Methods: 178 adult rats underwent facial nerve manipulation and testing. In the experimental groups, the left facial nerve was either crushed, transected and repaired epineurially, or transected and the stumps suture-secured into a tube with a 2 mm gap between them. Facial recovery was measured for the ensuing 1?4 months. Data were analyzed for whisking recovery. Previously developed markers of co-contraction of the upper and midfacial zones (possible synkinesis markers) were also examined. Results: Animals in the crush groups recovered nearly normal whisking parameters within 25 days. The distal branch crush group showed improved recovery over the main trunk crush group for several days during early recovery. By week 9, the transection/repair groups showed evidence of recovery that trended further upward throughout the study period. The entubulation groups followed a similar recovery pattern, though they did not maintain significant recovery levels by the study conclusion. Markers of potential synkinesis increased in selected groups following facial nerve injury. Conclusions: Rodent vibrissial function recovers in a predictable fashion following manipulation. Generalized co-contraction of the upper and midfacial zones emerges following facial nerve manipulation, possibly related to aberrant regeneration, polyterminal axons, or hypersensitivity of the rodent to sensory stimuli following nerve manipulation.
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