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Felix Benninger

Showing results (71-80 of 76) with videos related to

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Epilepsia|October 17, 2025
Paroxysmal slow wave events as a diagnostic biomarker for epilepsy: Lessons from rural ZambiaAndrew Malunga, Sina Lash, Alaa Abu-Ahmad, et al.
Epilepsia|November 6, 2024
Imaging blood-brain barrier dysfunction in drug-resistant epilepsy: A multi-center feasibility studyNir Cafri, Sheida Mirloo, Daniel Zarhin, et al.
Science Translational Medicine|December 6, 2019
Paroxysmal slow cortical activity in Alzheimer's disease and epilepsy is associated with blood-brain barrier dysfunctionDan Z Milikovsky, Jonathan Ofer, Vladimir V Senatorov, et al.
American Journal of Human Genetics|May 21, 2019
A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic EncephalopathyIngo Helbig, Tania Lopez-Hernandez, Oded Shor, et al.
Annals of Neurology|April 6, 2017
Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K<sup>+</sup> channel propertiesKaren L Oliver, Silvana Franceschetti, Carol J Milligan, et al.
Epilepsy & Behavior : E&B|December 30, 2021
International Post Stroke Epilepsy Research Consortium (IPSERC): A consortium to accelerate discoveries in preventing epileptogenesis after strokeNishant K Mishra, Jerome Engel, David S Liebeskind, et al.
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Showing results (71-80 of 76) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 76 results.
Epilepsia|October 17, 2025
Paroxysmal slow wave events as a diagnostic biomarker for epilepsy: Lessons from rural ZambiaAndrew Malunga, Sina Lash, Alaa Abu-Ahmad, et al.
Epilepsia|November 6, 2024
Imaging blood-brain barrier dysfunction in drug-resistant epilepsy: A multi-center feasibility studyNir Cafri, Sheida Mirloo, Daniel Zarhin, et al.
Science Translational Medicine|December 6, 2019
Paroxysmal slow cortical activity in Alzheimer's disease and epilepsy is associated with blood-brain barrier dysfunctionDan Z Milikovsky, Jonathan Ofer, Vladimir V Senatorov, et al.
American Journal of Human Genetics|May 21, 2019
A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic EncephalopathyIngo Helbig, Tania Lopez-Hernandez, Oded Shor, et al.
Annals of Neurology|April 6, 2017
Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K<sup>+</sup> channel propertiesKaren L Oliver, Silvana Franceschetti, Carol J Milligan, et al.
Epilepsy & Behavior : E&B|December 30, 2021
International Post Stroke Epilepsy Research Consortium (IPSERC): A consortium to accelerate discoveries in preventing epileptogenesis after strokeNishant K Mishra, Jerome Engel, David S Liebeskind, et al.
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