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Distraction produces an increase in pain-evoked anterior cingulate activity

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Increased contact heat pain and shortened latencies of contact heat evoked potentials following capsaicin-induced heat hyperalgesia

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Chapter 12 Clinical utility of pain - laser evoked potentials

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Laser evoked potentials using the Nd:YAG laser

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Clinical application of laser evoked potentials using the Nd:YAG laser

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Confidence of probabilistic predictions modulates the cortical response to pain

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Anodal Transcutaneous Spinal Direct Current Stimulation (tsDCS) Selectively Inhibits the Synaptic Efficacy of Nociceptive Transmission at Spinal Cord Level

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Electroencephalography During Nociceptive Stimulation in Chronic Pain Patients: A Systematic Review

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Dipole source analyses of laser evoked potentials obtained from subdural grid recordings from primary somatic sensory cortex

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Topiramate modulates habituation in migraine: evidences from nociceptive responses elicited by laser evoked potentials

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Electrophysiological indices of orienting attention toward pain

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Cortical responses to salient nociceptive and not nociceptive stimuli in vegetative and minimal conscious state

de Tommaso, M., Navarro, J., Lanzilotti, C., Ricci, K., Buonocunto, F., Livrea, P., & Lancioni, G. E. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00017 · Cited by 32

Parallel spinal pathways generate the middle-latency N1 and the late P2 components of the laser evoked potentials

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Les potentiels évoqués au laser thulium. Valeurs normatives aux membres supérieurs et inférieurs

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De novo artistic activity following insular–SII ischemia

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Distraction produces an increase in pain‐evoked anterior cingulate activity

Dowman, R. (2004) · Psychophysiology · doi:10.1111/j.1469-8986.2004.00186.x · Cited by 31

Laser-evoked potentials in human pain

Chen, A. C. N., Arendt‐Nielsen, L., & Plaghki, L. (1998) · Pain Forum · doi:10.1016/s1082-3174(98)70002-9 · Cited by 31

Somatosensory spatial attention modulates amplitudes, latencies, and latency jitter of laser-evoked brain potentials

Franz, M., Nickel, M. M., Ritter, A., Miltner, W. H. R., & Weiss, T. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00070.2015 · Cited by 28

Human primary somatosensory cortex is differentially involved in vibrotaction and nociception.

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Assessment of small fibers using evoked potentials

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Advances in diagnostics and outcome measures in peripheral neuropathies

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Normative data of contact heat evoked potentials from the lower extremities

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Source localisation of 62-electrode human laser pain evoked potential data using a realistic head model

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Effects of Distraction Versus Spatial Discrimination on Laser‐Evoked Potentials in Migraine

de Tommaso, M., Baumgärtner, U., Sardaro, M., et al. (2007) · Headache The Journal of Head and Face Pain · doi:10.1111/j.1526-4610.2007.00857.x · Cited by 28

Psychophysical and electrophysiological evidence for nociceptive dysfunction in complex regional pain syndrome

Caty, G. D., Hu, L., Legrain, V., Plaghki, L., & Mouraux, A. (2013) · Pain · doi:10.1016/j.pain.2013.07.038 · Cited by 28

Improved acquisition of contact heat evoked potentials with increased heating ramp

Schoenmacker, I. D., Archibald, J., Kramer, J. L. K., & Hubli, M. (2022) · Scientific Reports · doi:10.1038/s41598-022-04867-y · Cited by 27

Cortical correlates of an attentional bias to painful and innocuous somatic stimuli in children with recurrent abdominal pain

Hermann, C., Zohsel, K., Hohmeister, J., & Flor, H. (2008) · Pain · doi:10.1016/j.pain.2008.01.007 · Cited by 27

How Do Brain Areas Communicate During the Processing of Noxious Stimuli? An Analysis of Laser-Evoked Event-Related Potentials Using the Granger Causality Index

Weiß, T., Hesse, W., Ungureanu, M., Hecht, H., Leistritz, L., Witte, H., & Miltner, W. H. R. (2008) · Journal of Neurophysiology · doi:10.1152/jn.00912.2007 · Cited by 28

Short-term therapeutic effects of 890-nanometer light therapy for chronic low back pain: a double-blind randomized placebo-controlled study

Hsieh, R., & Lee, W. (2013) · Lasers in Medical Science · doi:10.1007/s10103-013-1378-2 · Cited by 26

Was it a pain or a sound? Across-species variability in sensory sensitivity

Hu, L., Xia, X. L., Peng, W., Su, W. X., Luo, F., Yuan, H., Chen, A. T., Liang, M., & Iannetti, G. D. (2015) · Pain · doi:10.1097/j.pain.0000000000000316 · Cited by 26

Cortical responses to noxious stimuli during sleep

Wang, X., Inui, K., Qiu, Y., & Kakigi, R. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.06.036 · Cited by 26

Attention to painful cutaneous laser stimuli evokes directed functional connectivity between activity recorded directly from human pain-related cortical structures

Liu, C.-C., Ohara, S., Franaszczuk, P. J., & Lenz, F. A. (2011) · Pain · doi:10.1016/j.pain.2010.12.016 · Cited by 26

Segmental inhibition of cutaneous heat sensation and of laser-evoked potentials by experimental muscle pain

Valeriani, M., Pera, D. L., Restuccia, D., et al. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.07.045 · Cited by 26

Cortical activity evoked by an acute painful tissue-damaging stimulus in healthy adult volunteers

Lorenzo Fabrizi, D., Williams, G., Lee, A., Meek, J. H., Slater, R., Olhede, S. C., & Fitzgerald, M. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00990.2012 · Cited by 25

Effects of aging on laser evoked potentials

Créac’h, C., Bertholon, A., Convers, P., Garcı́a-Larrea, L., & Peyron, R. (2014) · Muscle & Nerve · doi:10.1002/mus.24458 · Cited by 24

Electrophysiological correlates of reduced pain perception after theta-burst stimulation

Csifcsák, G., Nitsche, M. A., Baumgärtner, U., Paulus, W., Treede, R., & Antal, A. (2009) · Neuroreport · doi:10.1097/wnr.0b013e32832e0c74 · Cited by 24

Habituation of laser-evoked potentials by migraine phase: a blinded longitudinal study

Uglem, M., Omland, P. M., Stjern, M., Gravdahl, G. B., & Sand, T. (2017) · The Journal of Headache and Pain · doi:10.1186/s10194-017-0810-6 · Cited by 23

Neural mechanisms of detecting and orienting attention toward unattended threatening somatosensory targets. I. Intermodal effects

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Effect of sleep deprivation on the electrophysiological signature of habituation to noxious laser stimuli

Schuh‐Hofer, S., Baumgärtner, U., & Treede, R. (2015) · European Journal of Pain · doi:10.1002/ejp.698 · Cited by 26

The Pain-Evoked P2 Is Not a P3a Event-Related Potential

Dowman, R. (2004) · Brain Topography · doi:10.1023/b:brat.0000047332.24629.8e · Cited by 23

Expectation to feel more pain disrupts the habituation of laser-pain rating and laser-evoked potential amplitudes

Pazzaglia, C., Testani, E., Giordano, R., Padua, L., & Valeriani, M. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.07.027 · Cited by 23

Modulation of laser-evoked potentials and pain perception by transcutaneous electrical nerve stimulation (TENS): A placebo-controlled study in healthy volunteers

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Centrifugal modulation of human LEP components to a task-relevant noxious stimulation triggering voluntary movement

Nakata, H., Sakamoto, K., Honda, Y., Mochizuki, H., Hoshiyama, M., & Kakigi, R. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.11.026 · Cited by 22

Duration of the cue-to-pain delay increases pain intensity: a combined EEG and MEG study

Hauck, M., Lorenz, J., Zimmermann, R., Debener, S., Scharein, E., & Engel, A. K. (2007) · Experimental Brain Research · doi:10.1007/s00221-007-0863-x · Cited by 22

Early Detection of Small-Fiber Neuropathy in Diabetes

Pozzessere, G., Rossi, P., Gabriele, A., et al. (2002) · Diabetes Care · doi:10.2337/diacare.25.12.2355 · Cited by 22

The effect of smoking on pain-related evoked potentials

Miyazaki, T., Wang, X., Inui, K., et al. (2009) · Brain Research · doi:10.1016/j.brainres.2009.12.022 · Cited by 21

A review on the ongoing quest for a pain signature in the human brain

Su, Q., Song, Y., Zhao, R., & Liang, M. (2019) · Brain Science Advances · doi:10.26599/bsa.2019.9050024 · Cited by 25

Pain modulation in waking and hypnosis in women: event-related potentials and sources of cortical activity

De Pascalis, V., Varriale, V., & Cacace, I. (2015) · PLOS ONE · doi:10.1371/journal.pone.0128474 · Cited by 20

Cortical nociceptive processes are reduced by visual alpha‐band entrainment in the human brain

Ecsy, K., Brown, C. A., & Jones, A. K. P. (2017) · European Journal of Pain · doi:10.1002/ejp.1136 · Cited by 20

Multimodal approaches to laser-evoked potential generators

Garcı́a-Larrea, L. (1998) · Pain Forum · doi:10.1016/s1082-3174(98)80008-1 · Cited by 20

Increased brain responses during subjectively-matched mechanical pain stimulation in fibromyalgia patients as evidenced by MEG

Maestú, C., Cortes, A., Vazquez, J. M., del Río, D., Gómez-Argüelles, J. M., del Pozo, F., & Nevado, Á. (2012) · Clinical Neurophysiology · doi:10.1016/j.clinph.2012.09.015 · Cited by 19

Magnitude and Temporal Variability of Inter-stimulus EEG Modulate the Linear Relationship Between Laser-Evoked Potentials and Fast-Pain Perception

Li, L., Huang, G., Lin, Q., Liu, J., Zhang, S., & Zhang, Z. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00340 · Cited by 18

Reproducibility of contact heat evoked potentials (CHEPs) over a 6 months interval

Ruscheweyh, R., Emptmeyer, K., Putzer, D., Kropp, P. A., & Marziniak, M. (2013) · Clinical Neurophysiology · doi:10.1016/j.clinph.2013.05.003 · Cited by 18

Topographic Analysis of Painful Laser and Sural Nerve Electrical Evoked Potentials

Dowman, R. (2004) · Brain Topography · doi:10.1023/b:brat.0000019185.30489.ad · Cited by 18

Effects of Transcranial Direct Current Stimulation (t-DCS) of the Cerebellum on Pain Perception and Endogenous Pain Modulation: a Randomized, Monocentric, Double-Blind, Sham-Controlled Crossover Study

Stacheneder, R., Alt, L., Straube, A., & Ruscheweyh, R. (2022) · The Cerebellum · doi:10.1007/s12311-022-01498-x · Cited by 17

Expectations underlie the effects of unpredictable pain: a behavioral and electroencephalogram study

Pavy, F., Zaman, J., von Leupoldt, A., & Torta, D. M. E. (2023) · Pain · doi:10.1097/j.pain.0000000000003046 · Cited by 18

The characteristics of no-go potentials with intraepidermal stimulation

Nakata, H., Sakamoto, K., Inui, K., et al. (2009) · Neuroreport · doi:10.1097/wnr.0b013e32832f81d6 · Cited by 17

Normalization of Pain-Evoked Neural Reponses Using Spontaneous EEG Improves the Performance of EEG-Based Cross-Individual Pain Prediction

Bai, Y., Huang, G., Tu, Y., Tan, A., Hung, Y. S., & Zhang, Z. (2016) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2016.00031 · Cited by 17

Nociceptive-Evoked Potentials Are Sensitive to Behaviorally Relevant Stimulus Displacements in Egocentric Coordinates

Moayedi, M., Stefano, G. D., Stubbs, M. T., Djeugam, B., Liang, M., & Iannetti, G. D. (2016) · eNeuro · doi:10.1523/eneuro.0151-15.2016 · Cited by 17

Exogenous and endogenous components of ultralate (C-fibre) evoked potentials following CO2 laser stimuli to tiny skin surface areas in healthy subjects

Opsommer, E., Guérit, J., & Plaghki, L. (2003) · Neurophysiologie Clinique · doi:10.1016/s0987-7053(03)00007-8 · Cited by 17

Subliminal emotional pictures are capable of modulating early cerebral responses to pain in fibromyalgia

Peláez, I., Ferrera, D., Barjola, P., Fernandes-Magalhaes, R., & Mercado, F. (2019) · PLoS ONE · doi:10.1371/journal.pone.0217909 · Cited by 19

Chapter 30 Evoked potentials in the assessment of pain

Garcı́a-Larrea, L. (2006) · Handbook of clinical neurology · doi:10.1016/s0072-9752(06)80034-5 · Cited by 12

Contact Heat Evoked Potentials (CHEPs) in Patients with Mild-Moderate Alzheimer’s Disease and Matched Control—A Pilot Study

Jensen‐Dahm, C., Madsen, C. S., Waldemar, G., Ballegaard, M., Hejl, A., Johnsen, B., & Jensen, T. S. (2015) · Pain Medicine · doi:10.1093/pm/pnv012 · Cited by 16

Inhibition of Cortical Laser-Evoked Potentials by Transcutaneous Electrical Nerve Stimulation

Krabbenbos, I. P., Brandsma, D., van Swol, C. F. P., et al. (2009) · Neuromodulation Technology at the Neural Interface · doi:10.1111/j.1525-1403.2009.00204.x · Cited by 15

Cortical inhibition of laser pain and laser‐evoked potentials by non‐nociceptive somatosensory input

Testani, E., Pera, D. L., Percio, C. D., et al. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.13035 · Cited by 15

Do nociceptive stimulation intensity and temporal predictability influence pain-induced corticospinal excitability modulation?

Neige, C., Brun, C., Gagné, M., Bouyer, L. J., & Mercier, C. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.116883 · Cited by 13

Sympathetic skin response evoked by laser skin stimulation.

Rossi, P., Truini, A., Serrao, M., Iannetti, G. D., Parisi, L., Pozzessere, G., & Cruccu, G. (2002) · PubMed · Cited by 15

Imagerie fonctionnelle cérébrale appliquée à l’analyse des phénomènes douloureux

Peyron, R., & Faillenot, I. (2011) · médecine/sciences · doi:10.1051/medsci/201127182 · Cited by 15

Effect of Virtual Reality Hypnosis on Pain Threshold and Neurophysiological and Autonomic Biomarkers in Healthy Volunteers: Prospective Randomized Crossover Study

Terzulli, C., Melchior, M., Goffin, L., Faisan, S., Gianesini, C., Graff, D., Dufour, A., Laroche, É., Chauvin, C., & Poisbeau, P. (2022) · Journal of Medical Internet Research · doi:10.2196/33255 · Cited by 14

Awareness of Temperature and Pain Sensation

Valls‐Solé, J., Castellote, J. M., Köfler, M., Casanova‐Mollá, J., Kumru, H., & Schestatsky, P. (2012) · Journal of Pain · doi:10.1016/j.jpain.2011.11.003 · Cited by 14

Laser-evoked potentials for assessment of nociceptive pathways in humans

Treede, R., Magerl, W., & Baumgärtner, U. (1998) · Pain Forum · doi:10.1016/s1082-3174(98)80005-6 · Cited by 14

Statistical Modeling and Analysis of Laser-Evoked Potentials of Electrocorticogram Recordings from Awake Humans

Chen, Z. S., Ohara, S., Cao, J., et al. (2007) · Computational Intelligence and Neuroscience · doi:10.1155/2007/10479 · Cited by 13

Mortality salience modulates cortical responses to painful somatosensory stimulation: Evidence from slow wave and delta band activity

Valentini, E., Koch, K., Nicolardi, V., & Aglioti, S. M. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.07.025 · Cited by 12

Discrepancy between perceived pain and cortical processing: A voxel-based morphometry and contact heat evoked potential study

Kramer, J. L. K., Jutzeler, C. R., Haefeli, J., Curt, A. E. P., & Freund, P. (2015) · Clinical Neurophysiology · doi:10.1016/j.clinph.2015.02.054 · Cited by 13

Dyspnea-pain counterirritation induced by inspiratory threshold loading: a laser-evoked potentials study

Bouvier, G., Laviolette, L., Kindler, F., Naccache, L., Mouraux, A., Similowski, T., & Morélot‐Panzini, C. (2012) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01055.2011 · Cited by 12

Assessing pain in patients with chronic disorders of consciousness: Are we heading in the right direction?

Naro, A., Bramanti, P., Bramanti, A., & Calabrò, R. S. (2017) · Consciousness and Cognition · doi:10.1016/j.concog.2017.08.009 · Cited by 12

Distraction Reduces Both Early and Late Electrocutaneous Stimulus Evoked Potentials

Blom, J. H. G., Wiering, C. H., & Lubbe, R. H. J. V. D. (2012) · Journal of Psychophysiology · doi:10.1027/0269-8803/a000079 · Cited by 12

Conditioned pain modulation affects the N2/P2 complex but not the N1 wave: A pilot study with laser‐evoked potentials

Squintani, G. M., Rasera, A., Segatti, A., Concon, E., Bonetti, B., Valeriani, M., & Tinazzi, M. (2020) · European Journal of Pain · doi:10.1002/ejp.1693 · Cited by 11

Chapter 27 Are the processes reflected by late and ultra-late laser evoked potentials specific of nociception?

Mouraux, A., & Plaghki, L. (2006) · Supplements to Clinical neurophysiology · doi:10.1016/s1567-424x(09)70031-5 · Cited by 11

Innocuous Peripheral Nerve Stimulation Shifts Stimulus–Response Function of Painful Laser Stimulation in Man

Ristić, D., & Ellrich, J. (2013) · Neuromodulation Technology at the Neural Interface · doi:10.1111/ner.12133 · Cited by 11

Neuropathies sensitives des petites fibres : intérêt des potentiels évoqués laser

Créac’h, C., Convers, P., Robert, F., Antoine, J.-C. G., & Camdessanché, J. (2010) · Revue Neurologique · doi:10.1016/j.neurol.2010.08.011 · Cited by 10

Neuromagnetic SII responses do not fully reflect pain scale

Chen, W., Yuan, R.-Y., Shih, Y., Yeh, T., Hung, D. L., Wu, Z., Ho, L., & Lin, Y. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.12.015 · Cited by 11

Modulation of laser-evoked potentials by experimental cutaneous tonic pain

Valeriani, M., Tonali, P., Pera, D. L., Restuccia, D., Armas, L. D., C, D. V., Miliucci, R., Fiaschi, A., Vigevano, F., Arendt‐Nielsen, L., et al. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.03.007 · Cited by 11

Chapter 7 The role of secondary somatosensory cortex and insula in pain

Mauguı̀ere, F. (2004) · Supplements to Clinical neurophysiology · doi:10.1016/s1567-424x(09)70343-5 · Cited by 11

Synaptic mitochondria in aging and neurodegenerative diseases: Functional decline and vulnerability

Cicali, K. A., Torres, A. K., & Tapia-Rojas, C. (2026) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-24-01571 · Cited by 16

Small fiber neuropathy

Kool, D., Hoeijmakers, J. G. J., Waxman, S. G., & Faber, C. G. (2024) · International review of neurobiology · doi:10.1016/bs.irn.2024.10.001 · Cited by 10

Klinische Anwendung schmerzevozierter Potenziale

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Potentiels évoqués en neurologie : réponses normales

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Single-trial laser-evoked potentials feature extraction for prediction of pain perception

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Uncertain is worse

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A novel approach to identify time-frequency oscillatory features in electrocortical signals

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Attention, novelty, and pain

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Libération de la créativité artistique et neurologie : étude de trois cas

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Development of a tester for pain, temperature sensation and tactile sensation

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RECOVERY OF SENSATION IN SPLIT THICKNESS SKIN GRAFTS

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Fundamental study on formulation design of skin care products by modeling of tactile sensation

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Pruritus, Pain and Other Abnormal Skin Sensations

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