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Journal articles on the topic 'Cortico-cortical evoked potentials'

Author: Grafiati
Published: 4 June 2021
Last updated: 20 February 2023

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1

Keller, Corey J., Christopher J. Honey, Pierre Mégevand, Laszlo Entz, Istvan Ulbert, and Ashesh D. Mehta. "Mapping human brain networks with cortico-cortical evoked potentials." Philosophical Transactions of the Royal Society B: Biological Sciences 369, no. 1653 (2014): 20130528. http://dx.doi.org/10.1098/rstb.2013.0528.

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The cerebral cortex forms a sheet of neurons organized into a network of interconnected modules that is highly expanded in humans and presumably enables our most refined sensory and cognitive abilities. The links of this network form a fundamental aspect of its organization, and a great deal of research is focusing on understanding how information flows within and between different regions. However, an often-overlooked element of this connectivity regards a causal, hierarchical structure of regions, whereby certain nodes of the cortical network may exert greater influence over the others. Whil
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2

File, Bálint, Emília Tóth, Virág Bokodi, et al. "P243 Functional connectivity analysis of cortico-cortical evoked potentials." Clinical Neurophysiology 128, no. 9 (2017): e256. http://dx.doi.org/10.1016/j.clinph.2017.07.251.

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3

Bykanov, A. E., D. I. Pitskhelauri, O. Yu Titov, et al. "Broca’s area intraoperative mapping with cortico-cortical evoked potentials." Voprosy neirokhirurgii imeni N.N. Burdenko 84, no. 6 (2020): 49. http://dx.doi.org/10.17116/neiro20208406149.

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4

Yang, Ha-rin, Young-Shin Ra, and Yong Seo Koo. "Intraoperative monitoring of cortico-cortical evoked potentials of the frontal aslant tract in a patient with oligodendroglioma." Annals of Clinical Neurophysiology 24, no. 1 (2022): 21–25. http://dx.doi.org/10.14253/acn.2022.24.1.21.

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The newly identified frontal aslant tract (FAT) that connects the posterior Broca’s area to the supplementary motor area is known to be involved in speech and language functions. We successfully intraoperatively monitored FAT using cortico-cortical evoked potentials generated by single-pulse electrical cortical stimulation in a patient with oligodendroglioma.
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5

Silverstein, Brian H., Eishi Asano, Ayaka Sugiura, Masaki Sonoda, Min-Hee Lee, and Jeong-Won Jeong. "Dynamic tractography: Integrating cortico-cortical evoked potentials and diffusion imaging." NeuroImage 215 (July 2020): 116763. http://dx.doi.org/10.1016/j.neuroimage.2020.116763.

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6

Prime, David, Matthew Woolfe, Steven O’Keefe, David Rowlands, and Sasha Dionisio. "Quantifying volume conducted potential using stimulation artefact in cortico-cortical evoked potentials." Journal of Neuroscience Methods 337 (May 2020): 108639. http://dx.doi.org/10.1016/j.jneumeth.2020.108639.

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7

Prime, David, Matthew Woolfe, David Rowlands, Steven O’Keefe, and Sasha Dionisio. "Comparing connectivity metrics in cortico-cortical evoked potentials using synthetic cortical response patterns." Journal of Neuroscience Methods 334 (March 2020): 108559. http://dx.doi.org/10.1016/j.jneumeth.2019.108559.

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8

Kumaravelu, Karthik, Chintan S. Oza, Christina E. Behrend, and Warren M. Grill. "Model-based deconstruction of cortical evoked potentials generated by subthalamic nucleus deep brain stimulation." Journal of Neurophysiology 120, no. 2 (2018): 662–80. http://dx.doi.org/10.1152/jn.00862.2017.

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Parkinson’s disease is associated with altered neural activity in the motor cortex. Chronic high-frequency deep brain stimulation (DBS) of the subthalamic nucleus (STN) is effective in suppressing parkinsonian motor symptoms and modulates cortical activity. However, the anatomical pathways responsible for STN DBS-mediated cortical modulation remain unclear. Cortical evoked potentials (cEP) generated by STN DBS reflect the response of cortex to subcortical stimulation, and the goal of this study was to determine the neural origin of STN DBS-generated cEP using a two-step approach. First, we rec
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9

Mukae, Nobutaka, Riki Matsumoto, Katsuya Kobayashi, et al. "P3-1-2. Assessment of the atypical cortico-cortical evoked potentials." Clinical Neurophysiology 129, no. 5 (2018): e40. http://dx.doi.org/10.1016/j.clinph.2018.02.107.

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10

Guo, Zhi-hao, Bao-tian Zhao, Sheela Toprani, et al. "Epileptogenic network of focal epilepsies mapped with cortico-cortical evoked potentials." Clinical Neurophysiology 131, no. 11 (2020): 2657–66. http://dx.doi.org/10.1016/j.clinph.2020.08.012.

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11

Prime, D., M. Woolfe, A. Koenig, et al. "Quantifying epileptic connectivity using Cortico-Cortical Evoked Potentials and Similarity Metrics." Brain Stimulation 12, no. 2 (2019): 417. http://dx.doi.org/10.1016/j.brs.2018.12.350.

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12

Liberati, D., L. Bedarida, P. Brandazza, and S. Cerutti. "A model for the cortico-cortical neural interaction in multisensory-evoked potentials." IEEE Transactions on Biomedical Engineering 38, no. 9 (1991): 879–90. http://dx.doi.org/10.1109/10.83608.

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13

Trebaul, Lena, David Rudrauf, Anne-Sophie Job, et al. "Stimulation artifact correction method for estimation of early cortico-cortical evoked potentials." Journal of Neuroscience Methods 264 (May 2016): 94–102. http://dx.doi.org/10.1016/j.jneumeth.2016.03.002.

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14

Matsumoto, Riki, Akio Ikeda, Hidenao Fukuyama, and Ryosuke Takahashi. "Visualization of human brain network by means of cortico-cortical evoked potentials." Neuroscience Research 65 (January 2009): S33. http://dx.doi.org/10.1016/j.neures.2009.09.1684.

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15

Yamao, Y., R. Matsumoto, T. Kunieda, et al. "P503: Intraoperative language network monitoring by means of cortico-cortical evoked potentials." Clinical Neurophysiology 125 (June 2014): S184. http://dx.doi.org/10.1016/s1388-2457(14)50600-1.

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16

Zazio, Agnese. "Reliability of early TMS-evoked potentials as markers of cortico-cortical connectivity." Brain Stimulation 16, no. 1 (2023): 186. http://dx.doi.org/10.1016/j.brs.2023.01.213.

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17

Hass, Charles A., and Lindsey L. Glickfeld. "High-fidelity optical excitation of cortico-cortical projections at physiological frequencies." Journal of Neurophysiology 116, no. 5 (2016): 2056–66. http://dx.doi.org/10.1152/jn.00456.2016.

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Optogenetic activation of axons is a powerful approach for determining the synaptic properties and impact of long-range projections both in vivo and in vitro. However, because of the difficulty of measuring activity in axons, our knowledge of the reliability of optogenetic axonal stimulation has relied on data from somatic recordings. Yet, there are many reasons why activation of axons may not be comparable to cell bodies. Thus we have developed an approach to more directly assess the fidelity of optogenetic activation of axonal projections. We expressed opsins (ChR2, Chronos, or oChIEF) in th
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18

Guder, Stephanie, Benedikt M. Frey, Winifried Backhaus, et al. "The Influence of Cortico-Cerebellar Structural Connectivity on Cortical Excitability in Chronic Stroke." Cerebral Cortex 30, no. 3 (2019): 1330–44. http://dx.doi.org/10.1093/cercor/bhz169.

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Abstract Brain imaging has recently evidenced that the structural state of distinct reciprocal cortico-cerebellar fiber tracts, the dentato-thalamo-cortical tract (DTCT), and the cortico-ponto-cerebellar tract (CPCeT), significantly influences residual motor output in chronic stroke patients, independent from the level of damage to the corticospinal tract (CST). Whether such structural information might also directly relate to measures of cortical excitability is an open question. Eighteen chronic stroke patients with supratentorial ischemic lesions and 17 healthy controls underwent transcrani
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19

Giampiccolo, D., S. Parmigiani, F. Basaldella, et al. "Recording cortico-cortical evoked potentials of the human arcuate fasciculus under general anaesthesia." Clinical Neurophysiology 132, no. 8 (2021): 1966–73. http://dx.doi.org/10.1016/j.clinph.2021.03.044.

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20

Novitskaya, Y., M. Dümpelmann, and A. Schulze-Bonhage. "Asymmetric connectivity in the human temporal lobe assessed by cortico-cortical evoked potentials." Brain Stimulation 12, no. 2 (2019): 415. http://dx.doi.org/10.1016/j.brs.2018.12.341.

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21

Faturos, Nicholas, Julio Chapeton, Sara Inati, and Kareem Zaghloul. "Stable long-term functional connectivity predict multiple aspects of cortico-cortical evoked potentials." Brain Stimulation 16, no. 1 (2023): 381–82. http://dx.doi.org/10.1016/j.brs.2023.01.760.

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22

Yamao, Yukihiro, and Riki Matsumoto. "Intraoperative cortico-cortical evoked potentials for monitoring the arcuate fasciculus: Feasible under general anesthesia?" Clinical Neurophysiology 133 (January 2022): 175–76. http://dx.doi.org/10.1016/j.clinph.2021.07.033.

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23

Lega, Bradley, Sasha Dionisio, Patrick Flanigan, et al. "Cortico-cortical evoked potentials for sites of early versus late seizure spread in stereoelectroencephalography." Epilepsy Research 115 (September 2015): 17–29. http://dx.doi.org/10.1016/j.eplepsyres.2015.04.009.

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24

Ferreri, Florinda, David Ponzo, Taina Hukkanen, et al. "Human brain cortical correlates of short-latency afferent inhibition: a combined EEG–TMS study." Journal of Neurophysiology 108, no. 1 (2012): 314–23. http://dx.doi.org/10.1152/jn.00796.2011.

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When linking in time electrical stimulation of the peripheral nerve with transcranial magnetic stimulation (TMS), the excitability of the motor cortex can be modulated to evoke clear inhibition, as reflected by the amplitude decrement in the motor-evoked potentials (MEPs). This specific property, designated short-latency afferent inhibition (SAI), occurs when the nerve–TMS interstimulus interval (ISI) is approximately 25 ms and is considered to be a corticothalamic phenomenon. The aim of the present study was to use the electroencephalographic (EEG) responses to navigated-TMS coregistration to
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25

Osada, Takahiro, Antoine J. Molcard, Takeshi Matsuo, et al. "Intrasulcal ECoG approach to cortico-cortical connectivity using electrical stimulation-induced evoked potentials in macaques." Neuroscience Research 71 (September 2011): e97. http://dx.doi.org/10.1016/j.neures.2011.07.415.

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26

Prime, David, David Rowlands, Steven O'Keefe, and Sasha Dionisio. "Considerations in performing and analyzing the responses of cortico-cortical evoked potentials in stereo-EEG." Epilepsia 59, no. 1 (2017): 16–26. http://dx.doi.org/10.1111/epi.13939.

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27

Prime, D., M. Woolfe, S. O'Keefe, D. Rowlands, and S. Dionisio. "Defining brain connectivity using time series similarity measures: An application to cortico-cortical evoked potentials." Brain Stimulation 12, no. 2 (2019): 417. http://dx.doi.org/10.1016/j.brs.2018.12.349.

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28

Matsumoto, R. "S48-2 In vivo exploration of brain network by means of cortico-cortical evoked potentials." Clinical Neurophysiology 121 (October 2010): S68. http://dx.doi.org/10.1016/s1388-2457(10)60288-x.

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29

Huang, Chien-Chun, Cheng-Siu Chang, and Yue-Loong Hsin. "Time–frequency spectral analysis of cortico-cortical evoked potentials by means of Hilbert–Huang transform." Brain Stimulation 8, no. 2 (2015): 388. http://dx.doi.org/10.1016/j.brs.2015.01.242.

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30

Tamura, Yukie, Hiroshi Ogawa, Christoph Kapeller, et al. "Passive language mapping combining real-time oscillation analysis with cortico-cortical evoked potentials for awake craniotomy." Journal of Neurosurgery 125, no. 6 (2016): 1580–88. http://dx.doi.org/10.3171/2015.4.jns15193.

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OBJECTIVE Electrocortical stimulation (ECS) is the gold standard for functional brain mapping; however, precise functional mapping is still difficult in patients with language deficits. High gamma activity (HGA) between 80 and 140 Hz on electrocorticography is assumed to reflect localized cortical processing, whereas the cortico-cortical evoked potential (CCEP) can reflect bidirectional responses evoked by monophasic pulse stimuli to the language cortices when there is no patient cooperation. The authors propose the use of “passive” mapping by combining HGA mapping and CCEP recording without a
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31

Nakae, Takuro, Riki Matsumoto, Takeharu Kunieda, et al. "Connectivity Gradient in the Human Left Inferior Frontal Gyrus: Intraoperative Cortico-Cortical Evoked Potential Study." Cerebral Cortex 30, no. 8 (2020): 4633–50. http://dx.doi.org/10.1093/cercor/bhaa065.

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Abstract In the dual-stream model of language processing, the exact connectivity of the ventral stream to the anterior temporal lobe remains elusive. To investigate the connectivity between the inferior frontal gyrus (IFG) and the lateral part of the temporal and parietal lobes, we integrated spatiotemporal profiles of cortico-cortical evoked potentials (CCEPs) recorded intraoperatively in 14 patients who had undergone surgical resection for a brain tumor or epileptic focus. Four-dimensional visualization of the combined CCEP data showed that the pars opercularis (Broca’s area) is connected to
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32

Giampiccolo, Davide, Sara Parmigiani, Federica Basaldella, et al. "Reply to “Intraoperative cortico-cortical evoked potentials for monitoring the arcuate fasciculus: Feasible under general anesthesia?”." Clinical Neurophysiology 133 (January 2022): 177–78. http://dx.doi.org/10.1016/j.clinph.2021.09.006.

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33

Kobayashi, K., R. Matsumoto, K. Usami, et al. "Safety of single-pulse electrical stimulation for cortico-cortical evoked potentials in epileptic human cerebral cortex." Journal of the Neurological Sciences 381 (October 2017): 548. http://dx.doi.org/10.1016/j.jns.2017.08.3750.

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34

Kobayashi, Katsuya, Riki Matsumoto, Masao Matsuhashi, et al. "High frequency activity overriding cortico-cortical evoked potentials reflects altered excitability in the human epileptic focus." Clinical Neurophysiology 128, no. 9 (2017): 1673–81. http://dx.doi.org/10.1016/j.clinph.2017.06.249.

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35

Vega-Zelaya, Lorena, Paloma Pulido, Rafael G. Sola, and Jesús Pastor. "Intraoperative Cortico-Cortical Evoked Potentials for Monitoring Language Function during Brain Tumor Resection in Anesthetized Patients." Journal of Integrative Neuroscience 22, no. 1 (2023): 17. http://dx.doi.org/10.31083/j.jin2201017.

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36

Fuentealba, Pablo, Sylvain Crochet, Igor Timofeev, and Mircea Steriade. "Synaptic Interactions Between Thalamic and Cortical Inputs Onto Cortical Neurons In Vivo." Journal of Neurophysiology 91, no. 5 (2004): 1990–98. http://dx.doi.org/10.1152/jn.01105.2003.

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To study the interactions between thalamic and cortical inputs onto neocortical neurons, we used paired-pulse stimulation (PPS) of thalamic and cortical inputs as well as PPS of two cortical or two thalamic inputs that converged, at different time intervals, onto intracellularly recorded cortical and thalamocortical neurons in anesthetized cats. PPS of homosynaptic cortico-cortical pathways produced facilitation, depression, or no significant effects in cortical pathways, whereas cortical responses to thalamocortical inputs were mostly facilitated at both short and long intervals. By contrast,
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37

Ishankulov, T. A., G. V. Danilov, D. I. Pitskhelauri, et al. "Prediction of Postoperative Speech Dysfunctions in Neurosurgery Based on Cortico-Cortical Evoked Potentials and Machine Learning Technology." Sovremennye tehnologii v medicine 14, no. 1 (2022): 25. http://dx.doi.org/10.17691/stm2022.14.1.03.

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38

Merchant, Shabbir Hussain I., Eleni Frangos, Jacob Parker, et al. "The role of the inferior parietal lobule in writer’s cramp." Brain 143, no. 6 (2020): 1766–79. http://dx.doi.org/10.1093/brain/awaa138.

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Abstract Humans have a distinguishing ability for fine motor control that is subserved by a highly evolved cortico-motor neuronal network. The acquisition of a particular motor skill involves a long series of practice movements, trial and error, adjustment and refinement. At the cortical level, this acquisition begins in the parieto-temporal sensory regions and is subsequently consolidated and stratified in the premotor-motor cortex. Task-specific dystonia can be viewed as a corruption or loss of motor control confined to a single motor skill. Using a multimodal experimental approach combining
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39

Johnson, Graham, Kristin Wills, Leon Cai, et al. "ID:16588 Neural Network Trained on Distant Cortico-Cortical Evoked Potentials Can Localize Ictal Onset in Focal Epilepsy." Neuromodulation: Technology at the Neural Interface 25, no. 5 (2022): S106. http://dx.doi.org/10.1016/j.neurom.2022.02.124.

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40

Inoue, Takeshi, Hisashi Kawawaki, Masataka Fukuoka, et al. "Intraoperative cortico-cortical evoked potentials show disconnection of the motor cortex from the epileptogenic network during subtotal hemispherotomy." Clinical Neurophysiology 129, no. 2 (2018): 455–57. http://dx.doi.org/10.1016/j.clinph.2017.11.026.

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41

Matsuzaki, Naoyuki, Csaba Juhász, and Eishi Asano. "Cortico-cortical evoked potentials and stimulation-elicited gamma activity preferentially propagate from lower- to higher-order visual areas." Clinical Neurophysiology 124, no. 7 (2013): 1290–96. http://dx.doi.org/10.1016/j.clinph.2013.02.007.

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42

Kobayashi, Katsuya, Riki Matsumoto, Masao Matsuhashi, et al. "O1-E-9. HFO correlates of cortico-cortical evoked potentials reveal altered excitability in the human epileptic focus." Clinical Neurophysiology 124, no. 8 (2013): e30. http://dx.doi.org/10.1016/j.clinph.2013.02.075.

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43

Taylor, Kenneth N., Anand A. Joshi, Jian Li, et al. "The FAST graph: A novel framework for the anatomically-guided visualization and analysis of cortico-cortical evoked potentials." Epilepsy Research 161 (March 2020): 106264. http://dx.doi.org/10.1016/j.eplepsyres.2020.106264.

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44

Dümpelmann, M., Y. Novitskaya, and A. Schulze-Bonhage. "P62 Comparison of connectivity assessment in the human temporal lobe by cortico-cortical evoked potentials and granger causality." Clinical Neurophysiology 130, no. 8 (2019): e171. http://dx.doi.org/10.1016/j.clinph.2019.04.705.

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45

Rachidi, Inès, Lorella Minotti, Guillaume Martin, et al. "The Insula: A Stimulating Island of the Brain." Brain Sciences 11, no. 11 (2021): 1533. http://dx.doi.org/10.3390/brainsci11111533.

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Direct cortical stimulation (DCS) in epilepsy surgery patients has a long history of functional brain mapping and seizure triggering. Here, we review its findings when applied to the insula in order to map the insular functions, evaluate its local and distant connections, and trigger seizures. Clinical responses to insular DCS are frequent and diverse, showing a partial segregation with spatial overlap, including a posterior somatosensory, auditory, and vestibular part, a central olfactory-gustatory region, and an anterior visceral and cognitive-emotional portion. The study of cortico-cortical
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46

Saito, Taiichi, Manabu Tamura, Yoshihiro Muragaki, et al. "Intraoperative cortico-cortical evoked potentials for the evaluation of language function during brain tumor resection: initial experience with 13 cases." Journal of Neurosurgery 121, no. 4 (2014): 827–38. http://dx.doi.org/10.3171/2014.4.jns131195.

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Object The objective in the present study was to evaluate the usefulness of cortico-cortical evoked potentials (CCEP) monitoring for the intraoperative assessment of speech function during resection of brain tumors. Methods Intraoperative monitoring of CCEP was applied in 13 patients (mean age 34 ± 14 years) during the removal of neoplasms located within or close to language-related structures in the dominant cerebral hemisphere. For this purpose strip electrodes were positioned above the frontal language area (FLA) and temporal language area (TLA), which were identified with direct cortical s
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47

Cantone, Mariagiovanna, Giuseppe Lanza, Alice Le Pira, et al. "Adjunct Diagnostic Value of Transcranial Magnetic Stimulation in Mucopolysaccharidosis-Related Cervical Myelopathy: A Pilot Study." Brain Sciences 9, no. 8 (2019): 200. http://dx.doi.org/10.3390/brainsci9080200.

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Background: Cervical myelopathy (CM) is a common cause of morbidity and disability in patients with mucopolysaccharidosis (MPS) and, therefore, early detection is crucial for the best surgical intervention and follow-up. Transcranial magnetic stimulation (TMS) non-invasively evaluates the conduction through the cortico-spinal tract, also allowing preclinical diagnosis and monitoring. Methods: Motor evoked potentials (MEPs) to TMS were recorded in a group of eight patients with MPS-related CM. Responses were obtained during mild tonic muscular activation by means of a circular coil held on the
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48

Smith, A. T., and M. A. Gorassini. "Hyperexcitability of brain stem pathways in cerebral palsy." Journal of Neurophysiology 120, no. 3 (2018): 1428–37. http://dx.doi.org/10.1152/jn.00185.2018.

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Individuals with cerebral palsy (CP) experience impairments in the control of head and neck movements, suggesting dysfunction in brain stem circuitry. To examine if brain stem circuitry is altered in CP, we compared reflexes evoked in the sternocleidomastoid (SCM) muscle by trigeminal nerve stimulation in adults with CP and in age/sex-matched controls. Increasing the intensity of trigeminal nerve stimulation produced progressive increases in the long-latency suppression of ongoing SCM electromyography in controls. In contrast, participants with CP showed progressively increased facilitation ar
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49

Hardmeier, Martin, François Jacques, Philipp Albrecht, et al. "Multicentre assessment of motor and sensory evoked potentials in multiple sclerosis: reliability and implications for clinical trials." Multiple Sclerosis Journal - Experimental, Translational and Clinical 5, no. 2 (2019): 205521731984479. http://dx.doi.org/10.1177/2055217319844796.

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Background Motor and sensory evoked potentials (EP) are potential candidate biomarkers for clinical trials in multiple sclerosis. Objective To determine test -retest reliability of motor EP (MEP) and sensory EP (SEP) and associated EP-scores in patients with multiple sclerosis. Methods In three centres, 16 relapsing and five progressive multiple sclerosis patients had MEPs and SEPs 1–29 days apart. Five neurophysiologists independently marked latencies by central reading. By variance component analysis, we estimated the critical difference (absolute reliability) for cross-sectional group compa
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50

Boulogne, Sébastien, Nathalie Andre-Obadia, Vasilios K. Kimiskidis, Philippe Ryvlin, and Sylvain Rheims. "Cortico-cortical and motor evoked potentials to single and paired-pulse stimuli: An exploratory transcranial magnetic and intracranial electric brain stimulation study." Human Brain Mapping 37, no. 11 (2016): 3767–78. http://dx.doi.org/10.1002/hbm.23274.

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