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Komoltsev I.G.

Institute of Higher Nervous Activity and Neurophysiology RAS, Moscow, Russia;
Moscow Research and Clinical Center for Neuropsychiatry of the Healthcare Department, Moscow, Russia

Frankevich S.O.

Institute of Higher Nervous Activity and Neurophysiology RAS, Moscow, Russia

Shirobokova N.I.

Institute of Higher Nervous Activity and Neurophysiology RAS, Moscow, Russia

Volkova A.A.

Institute of Higher Nervous Activity and Neurophysiology RAS, Moscow, Russia

Levshina I.P.

Institute of Higher Nervous Activity and Neurophysiology RAS, Moscow, Russia

Novikova M.R.

Institute of Higher Nervous Activity and Neurophysiology RAS, Moscow, Russia

Manolova A.O.

Institute of Higher Nervous Activity and Neurophysiology RAS, Moscow, Russia

Guliaeva N.V.

Institute of Higher Nervous Activity and Neurophysiology of the Russian Academy of Sciences

Early electrophysiological consequences of dosed traumatic-brain injury in rats

Authors:

Komoltsev I.G., Frankevich S.O., Shirobokova N.I., Volkova A.A., Levshina I.P., Novikova M.R., Manolova A.O., Guliaeva N.V.

More about the authors

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To cite this article:

Komoltsev IG, Frankevich SO, Shirobokova NI, et al. Early electrophysiological consequences of dosed traumatic-brain injury in rats. S.S. Korsakov Journal of Neurology and Psychiatry. 2018;118(10‑2):21‑26. (In Russ.)
https://doi.org/10.17116/jnevro201811810221

References:

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  12. Rodgers KM, Dudek FE, Barth DS. Progressive, Seizure-Like, Spike-Wave Discharges Are Common in Both Injured and Uninjured Sprague-Dawley Rats: Implications for the Fluid Percussion Injury Model of Post-Traumatic Epilepsy. J Neurosci. 2015;35(24):9194-204 https://doi.org/10.1523/JNEUROSCI.0919-15.2015
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  14. Shaw F-Z, Liao Y-F. Relation between activities of the cortex and vibrissae muscles during high-voltage rhythmic spike discharges in rats. J Neurophysiol. 2005;93:2435-2448. https://doi.org/10.1152/jn.00999.2004
  15. D’Ambrosio R, Fender JS, Fairbanks JP, Simon EA, Born DE, Doyle DL, Miller JW. Progression from frontal-parietal to mesial-temporal epilepsy after fluid percussion injury in the rat. Brain. 2005;128:174-188. https://doi.org/10.1093/brain/awh337
  16. Vezzani A, Auvin S, Ravizza T, Aronica E. Glia-neuronal interactions in ictogenesis and epileptogenesis: role of inflammatory mediators. Jasper’s Basic Mech Epilepsies, 4th Ed; 2012.
  17. Grady MS, Charleston JS, Maris D, Witgen BM, Lifshitz J. Neuronal and glial cell number in the hippocampus after experimental traumatic brain injury: Analysis by stereological estimation. J Neurotrauma. 2003;20:929-941. https://doi.org/10.1089/089771503770195786
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  19. Komol’tsev IG, Volkova AA, Levshina IP, Novikova MR, Manolova AO, Stepanichev MYu, Gulyaeva NV. The Number of IgG-Positive Neurons in the Rat Hippocampus Increases after Dosed Traumatic Brain Injury. Neurochemical Journal. 2018;12(3):255-261. (In Russ.) https://doi.org/10.1134/S1027813318030056

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