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M Korff

Showing results (71-80 of 83) with videos related to

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Epilepsy Research|February 5, 2013
Tracking the source of cerebellar epilepsy: hemifacial seizures associated with cerebellar cortical dysplasiaAgustina M Lascano, Alia Lemkaddem, Cristina Granziera, et al.
Pharmacogenomics|September 10, 2011
ABCB1 polymorphisms and neuropsychiatric adverse events in oseltamivir-treated children during influenza H1N1/09 pandemiaArnaud G L'Huillier, Kuntheavy Ing Lorenzini, Pierre-Alex Crisinel, et al.
Developmental Medicine and Child Neurology|January 26, 2022
Pyridoxine or pyridoxal-5-phosphate treatment for seizures in glycosylphosphatidylinositol deficiency: A cohort studyAllan Bayat, Angel Aledo-Serrano, Antonio Gil-Nagel, et al.
Epilepsia|May 16, 2014
Towards the identification of a genetic basis for Landau-Kleffner syndromeJudith Conroy, Paul A McGettigan, Dara McCreary, et al.
Neuroimage. Clinical|January 5, 2021
Modulation of epileptic networks by transient interictal epileptic activity: A dynamic approach to simultaneous EEG-fMRIG R Iannotti, M G Preti, F Grouiller, et al.
Journal of Thermal Biology|December 24, 2025
Plasticity and regional heterothermy of upper thermal tolerance in the ring-necked snakeChristian L Cox, Kelly Lin Wuthrich, Dareen Aloudeh, et al.
Seizure|January 29, 2016
Effectiveness of antiepileptic therapy in patients with PCDH19 mutationsJan Lotte, Thomas Bast, Peter Borusiak, et al.
Epilepsia|January 7, 2021
The phenotypic spectrum of X-linked, infantile onset ALG13-related developmental and epileptic encephalopathyAlexandre N Datta, Nadia Bahi-Buisson, Thierry Bienvenu, et al.
Biorxiv : the Preprint Server for Biology|March 27, 2026
Comprehensive classification of HCN1 variants linked to neurodevelopmental disorders with and without epilepsyRoberta Castelli, Carla Marini, Alessandro Porro, et al.
Nature Genetics|March 10, 2015
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathySteffen Syrbe, Ulrike B S Hedrich, Erik Riesch, et al.
Pageof 9

Showing results (71-80 of 83) with videos related to

Sort By:
Pageof 9
Epilepsy Research|February 5, 2013
Tracking the source of cerebellar epilepsy: hemifacial seizures associated with cerebellar cortical dysplasiaAgustina M Lascano, Alia Lemkaddem, Cristina Granziera, et al.
Pharmacogenomics|September 10, 2011
ABCB1 polymorphisms and neuropsychiatric adverse events in oseltamivir-treated children during influenza H1N1/09 pandemiaArnaud G L'Huillier, Kuntheavy Ing Lorenzini, Pierre-Alex Crisinel, et al.
Developmental Medicine and Child Neurology|January 26, 2022
Pyridoxine or pyridoxal-5-phosphate treatment for seizures in glycosylphosphatidylinositol deficiency: A cohort studyAllan Bayat, Angel Aledo-Serrano, Antonio Gil-Nagel, et al.
Epilepsia|May 16, 2014
Towards the identification of a genetic basis for Landau-Kleffner syndromeJudith Conroy, Paul A McGettigan, Dara McCreary, et al.
Neuroimage. Clinical|January 5, 2021
Modulation of epileptic networks by transient interictal epileptic activity: A dynamic approach to simultaneous EEG-fMRIG R Iannotti, M G Preti, F Grouiller, et al.
Journal of Thermal Biology|December 24, 2025
Plasticity and regional heterothermy of upper thermal tolerance in the ring-necked snakeChristian L Cox, Kelly Lin Wuthrich, Dareen Aloudeh, et al.
Seizure|January 29, 2016
Effectiveness of antiepileptic therapy in patients with PCDH19 mutationsJan Lotte, Thomas Bast, Peter Borusiak, et al.
Epilepsia|January 7, 2021
The phenotypic spectrum of X-linked, infantile onset ALG13-related developmental and epileptic encephalopathyAlexandre N Datta, Nadia Bahi-Buisson, Thierry Bienvenu, et al.
Biorxiv : the Preprint Server for Biology|March 27, 2026
Comprehensive classification of HCN1 variants linked to neurodevelopmental disorders with and without epilepsyRoberta Castelli, Carla Marini, Alessandro Porro, et al.
Nature Genetics|March 10, 2015
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathySteffen Syrbe, Ulrike B S Hedrich, Erik Riesch, et al.
Pageof 9