Electrical brain stimulation for epilepsy

Safety, ethical considerations, and application guidelines for the use of transcranial magnetic stimulation in clinical practice and research

Rossi, S., Hallett, M., Rossini, P. M., & Pascual-Leone, A. (2009) · Clinical Neurophysiology · doi:10.1016/j.clinph.2009.08.016 · Cited by 5,367

Electrical stimulation of the anterior nucleus of thalamus for treatment of refractory epilepsy

Fisher, R. S., Salanova, V., Witt, T. C., Worth, R. M., Henry, T. R., Gross, R. E., Oommen, K. J., Osorio, I., Nazzaro, J. M., Labar, D., et al. (2010) · Epilepsia · doi:10.1111/j.1528-1167.2010.02536.x · Cited by 1,930

Effect on parkinsonian signs and symptoms of bilateral subthalamic nucleus stimulation

Limousin, P., Pollak, P., Benazzouz, A., Hoffmann, D., Bas, J. L., Perret, J., Benabid, A., & Broussolle, E. (1995) · The Lancet · doi:10.1016/s0140-6736(95)90062-4 · Cited by 1,480

Responsive cortical stimulation for the treatment of medically intractable partial epilepsy

Morrell, M. J. (2011) · Neurology · doi:10.1212/wnl.0b013e3182302056 · Cited by 1,282

Psychosomatic Disease and the "Visceral Brain": Recent Developments Bearing on the Papez Theory of Emotion

MACLEAN, P. D. (1949) · Psychosomatic Medicine · doi:10.1097/00006842-194911000-00003 · Cited by 1,203

Jasper's Basic Mechanisms of the Epilepsies

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Vagus nerve stimulation therapy for partial-onset seizures

Handforth, A., DeGiorgio, C. M., Schachter, S. C., Uthman, B. M., Naritoku, D. K., Tecoma, E. S., Henry, T. R., Collins, S. D., Vaughn, B. V., Gilmartin, R. C., et al. (1998) · Neurology · doi:10.1212/wnl.51.1.48 · Cited by 1,107

Long-term treatment with vagus nerve stimulation in patients with refractory epilepsy

Morris, G. L., Mueller, W. M., & The Vagus Nerve Stimulation Study Group E–E (1999) · Neurology · doi:10.1212/wnl.53.8.1731 · Cited by 727

Chronic Anterior Thalamus Stimulation for Intractable Epilepsy

Hodaie, M., Wennberg, R. A., Dostrovsky, J. O., & Lozano, A. M. (2002) · Epilepsia · doi:10.1046/j.1528-1157.2002.26001.x · Cited by 605

Evidence-based guideline update: Vagus nerve stimulation for the treatment of epilepsy

Morris, G. L., Gloss, D. S., Buchhalter, J., Mack, K. J., Nickels, K. C., & Harden, C. L. (2013) · Neurology · doi:10.1212/wnl.0b013e3182a393d1 · Cited by 450

Combined modulatory effects of excitatory interneurons and pre- and post-feedback inhibition microcircuits on absence seizures

Zhou, Y., Shu, Z., Zhu, R., Huang, G., Wang, Y., & Chai, Y. (2025) · Biomedical Signal Processing and Control · doi:10.1016/j.bspc.2025.107587 · Cited by 1

Pre-ictal causal connectivity reveals the epileptic network characteristics for deep brain stimulation

Wang, Y., Yu, T., Ma, Y., Cui, W., Wang, X., Ren, L., & Li, Y. (2025) · Neuroscience · doi:10.1016/j.neuroscience.2025.06.025 · Cited by 1

Geometrical‐ and Substrate‐Dependent Photo Response of Thin‐Film Silicon‐Based Biointerfaces

Li, L., Zhang, Y., Gao, Y., Wang, Y., Wang, S., Gao, X., Chen, K., Yin, L., Sheng, X., & Yao, D. (2025) · Small Methods · doi:10.1002/smtd.202501228 · Cited by 1

Ultrasound‐Triggered Biomimetic Piezo‐Nanoplatforms for Non‐Invasive Epilepsy Treatment

Li, J., Pan, X., Li, H., Ren, X., Tan, T., Wang, M., Zhu, J., Yu, Y., Wang, H., & Fan, Z. (2025) · Advanced Functional Materials · doi:10.1002/adfm.202518001 · Cited by 3

Adaptive neuromodulation dialogues: navigating current challenges and emerging innovations in neuromodulation system development

Lampert, F., Baker, M. R., Jensen, M. A., Ayyoubi, A. H., Bentler, C., Bowersock, J. L., Esteller, R., Herron, J. A., Johnson, G. W., Kipke, D. R., et al. (2025) · Journal of Neural Engineering · doi:10.1088/1741-2552/ae2359 · Cited by 1

Deep brain stimulation for epilepsy: optimal targeting and clinical outcomes

Hart, L. A., Warren, A. E. L., Pacheco-Barrios, N. V., Bahners, B. H., Madan, S., Neudorfer, C., Howard, C., Chua, M. M. J., Shon, Y. M., Freund, B. E., et al. (2025) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2025-337218 · Cited by 1

Toward model-based design of causal manipulations of brain circuits with high spatiotemporal precision

De, A., Kiani, R., & Mazzucato, L. (2026) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2025.101632 · Cited by 1

High Theta (4–10 Hz) power as a biomarker of inhibition during epileptogenesis in an animal model of mesial temporal lobe epilepsy

Lévesque, M., Li, F. R., Wang, S., & Avoli, M. (2026) · Experimental Neurology · doi:10.1016/j.expneurol.2026.115765 · Cited by 1

A method for creating frameless stereotactic frame in deep brain stimulation

Luo, P., Xiao, N., Zhang, Y., & Guo, S. (2014) · IEEE International Conference on Mechatronics and Automation (ICMA) · doi:10.1109/icma.2014.6885824 · Cited by 1

Compress or Interfere?

Abdellatif, A. A., Samara, L., Mohamed, A., Al-Ali, A., Erbad, A., & Guizani, M. (2019) · IEEE International Conference on Sensing, Communication, and Networking (SECON) · doi:10.1109/sahcn.2019.8824824 · Cited by 1

Next Generation Neural Interface Electronics

Williams, I., Leene, L. B., & Constandinou, T. G. (2022) · River Publishers eBooks · doi:10.1201/9781003337522-7 · Cited by 1

Advances in Early Surgical Treatment of Drug-Resistant Epilepsy in Children

文, 世. (2023) · Advances in Clinical Medicine · doi:10.12677/acm.2023.1351015 · Cited by 1

Heart rate variability as a preictal marker for determining the laterality of seizure onset zone in frontal lobe epilepsy

Lee, S., Kim, H., Kim, J. H., So, M., Kim, J. B., & Kim, D. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1373837 · Cited by 1

Case report: Bridging limbic network epilepsy with psychiatric, memory, and sleep comorbidities: case illustrations of reversible psychosis symptoms during continuous, high-frequency ANT-DBS

Wheeler, L., Worrell, S., Balzekas, I., Bilderbeek, J. A., Hermes, D., Croarkin, P. E., Messina, S. A., Gompel, J. J. V., Miller, K. J., Křemen, V., et al. (2024) · Frontiers in Network Physiology · doi:10.3389/fnetp.2024.1426743 · Cited by 2

Trends in Thalamic Stereoelectroencephalography Utilization During Phase II Monitoring in North America: A Survey

Alhourani, A., Ostrov, P. B., Schwalb, J. M., Yang, A. I., Palade, A. E., Chang, E. F., & Neimat, J. S. (2025) · Operative Neurosurgery · doi:10.1227/ons.0000000000001614 · Cited by 1

The Role of Stimulation Techniques

Schachter, S. C. (2015) · Neuropsychiatric symptoms of neurological disease · doi:10.1007/978-3-319-22159-5_19 · Cited by 1

Participation Of The Vegetative System On Paroxismality And Formation Of Posttraummatic Epilepsy

Stoyanov, O. M., Kolesnik, O. O., Mashchenko, S. S., Antonenko, S. A., & Kaptalan, A. O. (2016) · Journal of Education, Health and Sport (Kazimierz Wielki University in Bydgoszcz) · doi:10.5281/zenodo.845924 · Cited by 1

The cognitive and emotional effects of deep brain stimulation in patients with epilepsy – literature review

Potasz-Kulikowska, K. (2017) · Aktualności Neurologiczne · doi:10.15557/an.2017.0009 · Cited by 1

Neuromodulation devices nowadays

Rizea, R. E., Gheorghiţă, K. L., David, G., & Ciurea, A. V. (2019) · Romanian Neurosurgery · doi:10.33962/roneuro-2019-005 · Cited by 1

Peroxisomal Proliferator-Activated γ-Receptors: Participation in the Anti-Seizure Effects of Transcranial DC Stimulation of the Cerebellum

Godlevsky, L. S., & Pervak, M. P. (2019) · Neurophysiology · doi:10.1007/s11062-019-09786-9 · Cited by 1

Epileptic and Nonepileptic Seizures after Traumatic Brain Injury

Hamilton, K. T., & Parko, K. (2019) · Springer eBooks · doi:10.1007/978-3-030-22436-3_10 · Cited by 1

Insertable 256×256 ion image sensor for spatiotemporal pH recording

Lee, Y., Kimura, Y., Nakamura, Y., Noda, T., Takahashi, K., & Sawada, K. (2019) · IEEE Biomedical Circuits and Systems Conference (BioCAS) · doi:10.1109/biocas.2019.8918985 · Cited by 1

Deep Brain Stimulation of Anterior Thalamic Nuclei for Intractable Epilepsy in Thailand: Case Report

Boongird, A., Boongird, A., Khongkhatithum, C., Thampratankul, L., & Visudtibhan, A. (2016) · PubMed · Cited by 1

Investigational Devices for Epilepsy

Worrell, G. A., Brinkmann, B. H., & Gompel, J. J. V. (2020) · Springer eBooks · doi:10.1007/978-3-030-59078-9_39 · Cited by 1

New Horizons in Temporal Lobe Seizure Control

Velasco, A. L., Saucedo-Alvarado, P. E., Sánchez, M. A., Guzmán-Jiménez, D. E., González-Garcia, I., & Velasco, F. (2021) · Journal of Clinical Neurophysiology · doi:10.1097/wnp.0000000000000715 · Cited by 1

Epilepsy: A Stigma More than Disease

Iqbal, R. K. (2019) · Annals of Advanced Biomedical Sciences · doi:10.23880/aabsc-16000131 · Cited by 1

Coupling and stochasticity in mesoscopic brain dynamics

Jedynak, M. (2017) · doi:10.5821/dissertation-2117-105831 · Cited by 1

Intracranial interictal functional networks predict the effect of subacute cortical stimulation in focal epilepsyPreprint

Wang, Y., Taylor, P. N., Díaz-Díaz, J., Selway, R., Valentı́n, A., Alarcón, G., & Jiménez‐Jiménez, D. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/288019 · Cited by 1

Computational modelling and electrical stimulation for epilepsy surgery

Hebbink, J. (2019) · doi:10.3990/1.9789036548328 · Cited by 1

Effect of sinusoidal electrical cortical stimulation on brain cellsPreprint

Ryu, S., Kim, K., Seo, H., Cho, J., Park, J., Jun, S. C., & Kim, H.-I. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/855395 · Cited by 1

Transient targeting of hypothalamic orexin neurons alleviates seizures in a mouse model of epilepsyPreprint

Li, H., Viskaitis, P., Bracey, E. F., Peleg‐Raibstein, D., & Burdakov, D. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.18.541308 · Cited by 1

Probing hippocampal stimulation in experimental temporal lobe epilepsy with functional MRIPreprint

Schwaderlapp, N., Paschen, E., LeVan, P., von Elverfeldt, D., & Haas, C. A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.07.556678 · Cited by 1

Biophysically inspired mean-field model of neuronal populations driven by ion-exchange mechanismsPreprint

Rabuffo, G., Bandyopadhyay, A., Calabrese, C., Gudibanda, K., Depannemaecker, D., Takarabe, L. M., Chatterjee, S., Saggio, M. L., Desroches, M., Ivanov, A., et al. (2025) · eLife · doi:10.7554/elife.104249 · Cited by 1

A biointegrated living brain stimulator evokes specific neural signallingPreprint

Zhao, Q., Meng, Q., Peng, M., Lu, Z., Liu, Z. H., Jiang, X., Zheng, H., & Du, X. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.22.725279 · Cited by 1

Neurostimulation dans l’épilepsie

Kahane, P., Chabardès, S., & Depaulis, A. (2015) · Pratique Neurologique - FMC · doi:10.1016/j.praneu.2015.01.014

Datenlage zur intrakraniellen Neurostimulation nur verhalten optimistisch

Lutz, M. (2014) · DNP - Der Neurologe und Psychiater · doi:10.1007/s15202-014-0830-x

Considerations for Improving Cost Benefit of Deep Brain Stimulation for the Treatment of Chronic Neurologic Diseases

Velasco, F., & Velasco, A. L. (2015) · World Neurosurgery · doi:10.1016/j.wneu.2015.07.026

FUNCTIONAL ELECTRICAL STIMULATION FOR CONTROL OF EPILEPTIC SEIZURES

Jiao, J. (2015) · VBN Forskningsportal (Aalborg Universitet) · doi:10.5278/vbn.phd.med.00028

Managing epilepsy patients treated with deep brain stimulation

Salanova, V., Sabau, D., & Witt, T. C. (2015) · Cambridge University Press eBooks · doi:10.1017/cbo9781316026625.011

Chapter 13 Deep Brain Stimulation for Medically Refractory Epilepsy

Gibson, W. S. J., & Duffy, P. S. (2016) · Pan Stanford Publishing eBooks · doi:10.1201/9781315364759-14

Toward an Optogenetic Therapy for Epilepsy

Tønnesen, J., Ledri, M., & Kokaia, M. (2017) · Cambridge University Press eBooks · doi:10.1017/9781107281875.022

Hippocampal In Silico Models of Seizures and Epilepsy

Raikov, I., & Soltész, I. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-804066-9.00015-8

Network Models of Epilepsy-Related Pathological Structural and Functional Alterations in the Dentate Gyrus

Raikov, I., Plitt, M. H., & Soltész, I. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803784-3.00023-8

Nondrug Treatment for Refractory Status Epilepticus

Luan, G., & Wang, X. (2017) · Springer eBooks · doi:10.1007/978-981-10-5125-8_7

Resting-state connectivity predicts patient-specific effects of deep brain stimulation for Parkinson’s diseasePreprint

Chen, X., Zhang, C., Li, Y., Huang, P., Lv, Q., Yu, W., Chen, S., Sun, B., & Wang, Z. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/203406

Brain Hyperstimulation by Epileptic Seizures

Barros, V. N. (2017) · Hospice and Palliative Medicine International Journal · doi:10.15406/hpmij.2017.01.00035

Die Tiefe Hirnstimulation bei medikamentös therapieschwieriger Epilepsie

Kudernatsch, M., & Arnold, S. (2018) · Das Neurophysiologie-Labor · doi:10.1016/j.neulab.2018.05.001

Synchronous Responses of Population Neurons to the Changes of Inter-Pulse-Intervals during Stimulations of Afferent Fibers

Ma, W., Feng, Z., Hu, H., Wang, Z., & Zhou, W. (2018) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc.2018.8512625

Noise-Assisted MEMD-Based Phase-Connectivity Analysis to Personalize Closed-Loop DBS Therapy in Epilepsy PatientsPreprint

Farahmand, S., Sobayo, T., & Mogul, D. J. (2019) · medRxiv · doi:10.1101/19006908

Stimulation Therapies for Epilepsy

King‐Stephens, D., & Weber, P. B. (2019) · Cambridge University Press eBooks · doi:10.1017/9781108754200.024

Use of Optogenetic Methods to Study and Suppress Epileptic Activity (review)

Smirnova, E. Y., & Zaitsev, A. V. (2019) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-019-00842-9

An Improved Intermittent Electrical Stimulation Therapy for Penicillin-induced Seizure Suppression

Liu, L., Zhang, J., Ye, S., & Xu, K. (2019) · International Conference on Biomedical and Bioinformatics Engineering (ICBBE) · doi:10.1145/3375923.3375930

Non Linear Analysis of the Effect of Stimulation on Epileptic Signals Generated at Right Hippocampus

Kataru, S. D., & Sunitha, R. (2020) · Communications in computer and information science · doi:10.1007/978-981-15-4828-4_31

Deep Brain Stimulation Approach in Neurological Diseases

Priya, D., & Abhishek, P. (2020) · IntechOpen eBooks · doi:10.5772/intechopen.91756

Epilepsy-associated mutations in GABRG2: characterization and therapeutic opportunities

Huang, X. (2014)

Opto-Magneto-Electrical Nanoactuators for Wireless Cell Stimulation

Zhang, Y. (2020) · Tesis Doctorals en Xarxa (Consorci de Serveis Universitaris de Catalunya)

A memristor-based neuromodulation device for real-time monitoring and adaptive control of in vitro neuronal populationsPreprint

Dias, C., Castro, D., Aroso, M., Ventura, J. O., & Aguiar, P. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.05.20.444941

Drug Resistance in Epilepsy: Which Prospect to Tame its Stubbornness?

Margineanu, D. G. (2021) · Medical Research Archives · doi:10.18103/mra.v9i8.2514

Determining the Role of Synchrony Dynamics in Epileptic Brain Networks

Sobayo, T., Farahmand, S., & Mogul, D. J. (2022) · Handbook of Neuroengineering · doi:10.1007/978-981-15-2848-4_71-2

Mapping and zapping

Schaper, F. (. L. W. V. J. ). (2022) · doi:10.26481/dis.20221103fs

Adaptive Supervisory Control of Epilepsy in a Neural Mass Model

Yang, M., Wang, J., Liu, C., & Yue, W. (2022) · Chinese Control Conference (CCC) · doi:10.23919/ccc55666.2022.9901936

Surgical modification of deep brain stimulation lead trajectories substantially reduces RF heating during MRI at 3 T: From phantom experiments to clinical applicationsPreprint

Vu, J., Bhusal, B., Rosenow, J. M., Pilitsis, J. G., & Golestanirad, L. (2022) · medRxiv · doi:10.1101/2022.12.22.22283839

C-Met Receptors Deficiency Was Involved in Absence Seizures Development in WAG/Rij Rats

Amiri, M., Ghorbani, S., Zavvari, F., Ravandi, H. H., & Karimzadeh, F. (2023) · Archives of Neuroscience · doi:10.5812/ans-132959

Quality Management Systems for Neural Engineering: Principles and Practices

Křemen, V., Jamshed, F., Benjamin, B., Worrel, G. A., Starr, P. A., Leyde, K. W., & Denison, T. (2023) · Handbook of Neuroengineering · doi:10.1007/978-981-16-5540-1_138

Neuronal wires and novel epileptic gene studies: Methods and mechanism of brain network and - Recent update

Rajendran, M. S., Prabhakaran, R., Ahalliya, R. M., Muthusami, S., Kannappan, P., Raju, M. V., & Chandrasekaran, M. K. (2023) · Human Gene · doi:10.1016/j.humgen.2023.201186

A 64-Channel sub-1nC Charge-balanced Stimulator IC for Seizure SuppressionPreprint

Lee, S., Kim, B., & Bae, J. (2023) · doi:10.22541/au.168499267.77703555/v1

Épilepsie

Vlaicu, M. B. ̆., & Vlaicu, A. (2023) · Elsevier eBooks · doi:10.1016/b978-2-294-77862-9.00007-4

An Adaptive Fuzzy Closed-loop Control of Neural Activity Based on Neural Mass Model

Ma, L., Li, S., & Tang, X. (2023) · International Congress on Image and Signal Processing (CISP) · doi:10.1109/cisp-bmei60920.2023.10373242

Estimulación hipocampal de baja y alta frecuencia en la epilepsia del lóbulo temporal mesial fármaco resistente.

Lim, S., Lee, C.-Y., Lee, S., Tu, P., Chang, B., Lee, C., Cheng, M.-Y., Chang, C., Tseng, W.-E. J., Hsieh, H., et al. (2016) · NeuroTarget · doi:10.47924/neurotarget2016176

Advancements in micro- and nanoelectronic devices for minimally invasive disease diagnosis and treatment

Huang, S., Chen, J., Huang, X., He, M., Liu, Z., Yao, C., Xu, X., Liu, J., Jiang, L., Chen, H.-J., et al. (2024) · Chinese Science Bulletin (Chinese Version) · doi:10.1360/tb-2024-0643 · Cited by 1

Modeling Generalized Tonic-Clonic Seizures with Coupled FitzHugh Oscillators

Orozco, Y., & Padilla-Longoria, P. (2025) · Springer eBooks · doi:10.1007/978-3-030-93954-0_11-1

fMRI in Epilepsy

Morgan, V. L. (2025) · Neuromethods · doi:10.1007/978-1-0716-4438-6_25

Neuromodulation in Epilepsy

Chiu, M. Y., & Rotenberg, A. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-10944-7.00100-1

Delta—fast ripple coupling suppression: designing a brain-mimetic stimulation paradigm for seizure abolishment

Tufa, U., Dian, J. A., Zahra, A., Wu, C., Zhang, L., Carlen, P. L., & Bardakjian, B. L. (2025) · Frontiers in Neuroscience · doi:10.3389/fnins.2025.1619278

Interactive Biomaterials

Liu, Z., Kong, X., & Shi, Y. (2025) · Springer eBooks · doi:10.1007/978-981-96-8646-9_7

Seizure incidence after deep brain stimulation: a meta-analysis of risk factors and target-specific outcomes in non-epileptic disorders

Bahadori, A. R., Javadnia, P., Naghavi, E., Heidaresfahani, L., Sarmadi, I., Rajabi, M., Davari, A., Dahaghin, S., Ranji, S., Shafiee, S., et al. (2025) · Neurosurgical Review · doi:10.1007/s10143-025-03727-3

The dynamic influence of temperature and electrical stimulation on seizures

Zeng, W., & Du, Y. (2025) · Nonlinear Dynamics · doi:10.1007/s11071-025-11665-4

Special Considerations for Personalization in Pediatric Intracranial Neuromodulation

Joshi, C. (2025) · Journal of Clinical Neurophysiology · doi:10.1097/wnp.0000000000001193

Dynamics study of double-column model and its application in epilepsy EEG

Xu, Y., Du, Y., Xu, X., & Wang, Y. (2025) · Cognitive Neurodynamics · doi:10.1007/s11571-025-10334-x

Individualized Target Selection of Closed-Loop Electrical Stimulation for the Treatment of Spontaneous Temporal Lobe Epilepsy

Yang, Y., Ni, H., Sun, Y., Xing, Y., Wang, C., Zhang, J., Zhu, J., & Xu, K. (2025) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2025.3614867

Reducing artifacts during human intracranial electrical stimulation by separating current return from recording ground

Oswalt, D. N., Beauchamp, M. S., Chen, H.-C. I., & Yoshor, D. (2025) · Brain stimulation · doi:10.1016/j.brs.2025.10.017

Electrochemical Impedance Behavior under Various Test Configurations for Electrodes in Implantable Neurostimulators

Liu, Y.-T., & Wang, H. (2025) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc58623.2025.11252933

Avances en el tratamiento de la epilepsia refractaria: estimulación cerebral profunda

Ciraolo, C. A. (2016) · Revista del Hospital Italiano de Buenos Aires · doi:10.51987/rev.hosp.ital.b.aires.v36i4.634

Additional file 1 of Automated calibration of somatosensory stimulation using reinforcement learning

Borda, L., Gozzi, N., Preatoni, G., Valle, G., & Raspopović, S. (2024) · Figshare · doi:10.6084/m9.figshare.26620018

Cerebellar deep brain stimulation rescues Purkinje cell mitochondrial density in a genetic mouse model of cerebellar ataxia

Miterko, L. N., Peacoe, L. E., Duraine, L., Zuo, Z., & Sillitoe, R. V. (2025) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2025.111704

Ion dynamics underlying the seizure delay effect of low-frequency electrical stimulation

Girier, G., Dallmer‐Zerbe, I., Chvojka, J., Kudláček, J., Jiruška, P., Hlinka, J., & Schmidt, H. (2025) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1013838

Computational modeling of seizure reconstruction and attenuation via model reference control

Brogin, J. A. F., Faber, J., Ryvlin, P., & Bueno, D. (2026) · Scientific Reports · doi:10.1038/s41598-026-39645-7

Deep brain stimulation in epilepsy

Lehtimäki, K. A., Mattila, H., & Peltola, J. (2026) · Elsevier eBooks · doi:10.1016/b978-0-323-99742-3.00014-x

Control of cortical population activity with patterned microstimulationPreprint

Barzon, G., De, A., Morán, I., Carnahan, C., Mazzucato, L., & Kiani, R. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.02.709018 · Cited by 1

A guide to neuromodulation in drug‐resistant epilepsy

Parikh, P., Dolezawa, I., Hegde, M., Imbach, L., Lundstrom, B. N., Pizzo, F., Rao, V. R., Singh, J., Southwell, D. G., Watanabe, S., et al. (2026) · Epileptic Disorders · doi:10.1002/epd2.70221

Validation d'une nouvelle électrode hybride intracérébrale comportant des tétrodes dans l'épilepsie pharmaco-résistante

Despouy, E. (2019) · theses.fr (ABES) · doi:10.70675/5903e0fdz9e05z4aa9z8acazb5f1f807aff8

Neurophysiological biomarkers of epileptogenic networks in intracranial (stereoelectroencephalography-SEEG) and simultaneous SEEG-magnetoelectroencephalography recordings

Pizzo, F. (2019) · theses.fr (ABES) · doi:10.70675/47b18bd1z793cz4149z98c7z893c06a659ca

Seizure onset patterns and functional inter-ictal connectivity in focal epilepsies : SEEG studies

Lagarde, S. (2020) · doi:10.70675/28daf5c8za991z40d6zb9b1z150d938daff0

Chronic Subthreshold Cortical Stimulation for Paracentral Epilepsy—A Systematic Review

Türk, B. G., Heyndrickx, S., Vonck, K. E. J., Boon, P., Roost, D. V., & Meurs, A. (2026) · Neuromodulation Technology at the Neural Interface · doi:10.1016/j.neurom.2026.02.003

Seizure outcomes after thalamic deep brain stimulation in drug‐resistant epilepsy: How electrode location, device platform, and epilepsy subtype drive response—A systematic review with pooled analysis

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