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Holger Lerche

Showing results (71-80 of 282) with videos related to

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Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 5, 2017
Motor cortex excitability in seizure-free STX1B mutation carriers with a history of epilepsy and febrile seizuresMaria-Ioanna Stefanou, Debora Desideri, Justus Marquetand, et al.
Epilepsy & Behavior : E&B|May 31, 2011
Antiepileptic drug therapy: does mechanism of action matter?Martin Brodie, Thanos Covanis, Antonio Gil-Nagel, et al.
Brain Topography|October 10, 2014
Differences between MEG and high-density EEG source localizations using a distributed source model in comparison to fMRISilke Klamer, Adham Elshahabi, Holger Lerche, et al.
Ebiomedicine|September 27, 2021
Distinct gene-set burden patterns underlie common generalized and focal epilepsiesMahmoud Koko, Roland Krause, Thomas Sander, et al.
Brain : a Journal of Neurology|October 27, 2025
USP25 in genetic generalized epilepsy: a gene under scrutinyMaryam Erfanian Omidvar, Jill R Murrell, Anna J Prentice, et al.
JCI Insight|November 25, 2016
Activity of Na<sub>V</sub>1.2 promotes neurodegeneration in an animal model of multiple sclerosisBenjamin Schattling, Walid Fazeli, Birgit Engeland, et al.
Biophysical Journal|March 4, 2006
Modeling of single noninactivating Na+ channels: evidence for two open and several fast inactivated statesYu-Kai The, Jacqueline Fernandes, M Oana Popa, et al.
The European Journal of Neuroscience|July 21, 2005
Molecular analysis of the A322D mutation in the GABA receptor alpha-subunit causing juvenile myoclonic epilepsyKlaus Krampfl, Snezana Maljevic, Patrick Cossette, et al.
Brain : a Journal of Neurology|March 26, 2002
Enhanced inactivation and pH sensitivity of Na(+) channel mutations causing hypokalaemic periodic paralysis type IIAlexey Kuzmenkin, Vanesa Muncan, Karin Jurkat-Rott, et al.
Epilepsy Research|January 12, 2007
Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsyAnne Hempelmann, Joana Cobilanschi, Armin Heils, et al.
Pageof 29

Showing results (71-80 of 282) with videos related to

Sort By:
Pageof 29
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 5, 2017
Motor cortex excitability in seizure-free STX1B mutation carriers with a history of epilepsy and febrile seizuresMaria-Ioanna Stefanou, Debora Desideri, Justus Marquetand, et al.
Epilepsy & Behavior : E&B|May 31, 2011
Antiepileptic drug therapy: does mechanism of action matter?Martin Brodie, Thanos Covanis, Antonio Gil-Nagel, et al.
Brain Topography|October 10, 2014
Differences between MEG and high-density EEG source localizations using a distributed source model in comparison to fMRISilke Klamer, Adham Elshahabi, Holger Lerche, et al.
Ebiomedicine|September 27, 2021
Distinct gene-set burden patterns underlie common generalized and focal epilepsiesMahmoud Koko, Roland Krause, Thomas Sander, et al.
Brain : a Journal of Neurology|October 27, 2025
USP25 in genetic generalized epilepsy: a gene under scrutinyMaryam Erfanian Omidvar, Jill R Murrell, Anna J Prentice, et al.
JCI Insight|November 25, 2016
Activity of Na<sub>V</sub>1.2 promotes neurodegeneration in an animal model of multiple sclerosisBenjamin Schattling, Walid Fazeli, Birgit Engeland, et al.
Biophysical Journal|March 4, 2006
Modeling of single noninactivating Na+ channels: evidence for two open and several fast inactivated statesYu-Kai The, Jacqueline Fernandes, M Oana Popa, et al.
The European Journal of Neuroscience|July 21, 2005
Molecular analysis of the A322D mutation in the GABA receptor alpha-subunit causing juvenile myoclonic epilepsyKlaus Krampfl, Snezana Maljevic, Patrick Cossette, et al.
Brain : a Journal of Neurology|March 26, 2002
Enhanced inactivation and pH sensitivity of Na(+) channel mutations causing hypokalaemic periodic paralysis type IIAlexey Kuzmenkin, Vanesa Muncan, Karin Jurkat-Rott, et al.
Epilepsy Research|January 12, 2007
Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsyAnne Hempelmann, Joana Cobilanschi, Armin Heils, et al.
Pageof 29