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Eva Andermann

Showing results (31-40 of 70) with videos related to

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Neurogenetics|May 27, 2005
Identification of a VPS13A founder mutation in French Canadian families with chorea-acanthocytosisCarol Dobson-Stone, Antonio Velayos-Baeza, An Jansen, et al.
Epilepsy & Behavior : E&B|April 1, 2018
Psychiatric and cognitive adverse events: A pooled analysis of three phase III trials of adjunctive eslicarbazepine acetate for partial-onset seizuresEva Andermann, Victor Biton, Selim R Benbadis, et al.
Annals of Neurology|January 2, 2003
An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindredFrançois Gros-Louis, Inge A Meijer, Collette K Hand, et al.
Epilepsia|April 17, 2013
SCN1A testing for epilepsy: application in clinical practiceShinichi Hirose, Ingrid E Scheffer, Carla Marini, et al.
Epilepsy Research|December 18, 2020
Comparative analysis of the safety and tolerability of eslicarbazepine acetate in older (≥60 years) and younger (18-59 years) adultsEva Andermann, William Rosenfeld, Patricia Penovich, et al.
Epilepsia|May 9, 2007
Surgical outcome in tuberous sclerosis complex: a multicenter surveyDeepak Madhavan, Sarah Schaffer, Alexei Yankovsky, et al.
Lancet (London, England)|September 24, 2002
Sodium-channel defects in benign familial neonatal-infantile seizuresSarah E Heron, Kathryn M Crossland, Eva Andermann, et al.
Brain : a Journal of Neurology|September 15, 2004
Action myoclonus-renal failure syndrome: characterization of a unique cerebro-renal disorderAmanPreet Badhwar, Samuel F Berkovic, John P Dowling, et al.
European Journal of Human Genetics : EJHG|January 11, 2020
Autosomal-dominant adult neuronal ceroid lipofuscinosis caused by duplication in DNAJC5 initially missed by Sanger and whole-exome sequencingIvana Jedličková, Maxime Cadieux-Dion, Anna Přistoupilová, et al.
Epilepsy Research|November 17, 2009
Suggestive evidence for a new locus for epilepsy with heterogeneous phenotypes on chromosome 17qAuli Sirén, Anne Polvi, Lyne Chahine, et al.
Pageof 7

Showing results (31-40 of 70) with videos related to

Sort By:
Pageof 7
Neurogenetics|May 27, 2005
Identification of a VPS13A founder mutation in French Canadian families with chorea-acanthocytosisCarol Dobson-Stone, Antonio Velayos-Baeza, An Jansen, et al.
Epilepsy & Behavior : E&B|April 1, 2018
Psychiatric and cognitive adverse events: A pooled analysis of three phase III trials of adjunctive eslicarbazepine acetate for partial-onset seizuresEva Andermann, Victor Biton, Selim R Benbadis, et al.
Annals of Neurology|January 2, 2003
An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindredFrançois Gros-Louis, Inge A Meijer, Collette K Hand, et al.
Epilepsia|April 17, 2013
SCN1A testing for epilepsy: application in clinical practiceShinichi Hirose, Ingrid E Scheffer, Carla Marini, et al.
Epilepsy Research|December 18, 2020
Comparative analysis of the safety and tolerability of eslicarbazepine acetate in older (≥60 years) and younger (18-59 years) adultsEva Andermann, William Rosenfeld, Patricia Penovich, et al.
Epilepsia|May 9, 2007
Surgical outcome in tuberous sclerosis complex: a multicenter surveyDeepak Madhavan, Sarah Schaffer, Alexei Yankovsky, et al.
Lancet (London, England)|September 24, 2002
Sodium-channel defects in benign familial neonatal-infantile seizuresSarah E Heron, Kathryn M Crossland, Eva Andermann, et al.
Brain : a Journal of Neurology|September 15, 2004
Action myoclonus-renal failure syndrome: characterization of a unique cerebro-renal disorderAmanPreet Badhwar, Samuel F Berkovic, John P Dowling, et al.
European Journal of Human Genetics : EJHG|January 11, 2020
Autosomal-dominant adult neuronal ceroid lipofuscinosis caused by duplication in DNAJC5 initially missed by Sanger and whole-exome sequencingIvana Jedličková, Maxime Cadieux-Dion, Anna Přistoupilová, et al.
Epilepsy Research|November 17, 2009
Suggestive evidence for a new locus for epilepsy with heterogeneous phenotypes on chromosome 17qAuli Sirén, Anne Polvi, Lyne Chahine, et al.
Pageof 7