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Ingrid E Scheffer

Showing results (251-260 of 586) with videos related to

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Epilepsia|October 20, 2020
Fenfluramine HCl (Fintepla<sup>®</sup> ) provides long-term clinically meaningful reduction in seizure frequency: Analysis of an ongoing open-label extension studyJoseph Sullivan, Ingrid E Scheffer, Lieven Lagae, et al.
Neurology|August 30, 2019
Efficacy and tolerability of adjunctive lacosamide in pediatric patients with focal seizuresViktor Farkas, Barbara Steinborn, J Robert Flamini, et al.
Epilepsia|January 7, 2012
Clinical genetic studies in benign childhood epilepsy with centrotemporal spikesDanya F Vears, Meng-Han Tsai, Lynette G Sadleir, et al.
Frontiers in Neurology|April 1, 2022
Impaired Color Recognition in <i>HCN1</i> Epilepsy: A Single Case ReportChaseley E Mckenzie, Chen-Jui Ho, Ian C Forster, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 21, 2010
Detection of microchromosomal aberrations in refractory epilepsy: a pilot studyJacinta M McMahon, Ingrid E Scheffer, Jillian K Nicholl, et al.
European Journal of Human Genetics : EJHG|May 16, 2025
Understanding speech and language in KIF1A-associated neurological disorderLottie D Morison, Adam P Vogel, John Christodoulou, et al.
NAR Genomics and Bioinformatics|April 7, 2025
Identifying individuals with rare disease variants by inferring shared ancestral haplotypes from SNP array dataErandee Robertson, Bronwyn E Grinton, Karen L Oliver, et al.
The Lancet. Neurology|May 23, 2006
De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective studySamuel F Berkovic, Louise Harkin, Jacinta M McMahon, et al.
Translational Psychiatry|May 6, 2020
A standardized patient-centered characterization of the phenotypic spectrum of PCDH19 girls clustering epilepsyKristy L Kolc, Lynette G Sadleir, Christel Depienne, et al.
Epilepsia|November 18, 2020
Transcriptome analysis of a ring chromosome 20 patient cohortKenneth A Myers, Mark F Bennett, Michael S Hildebrand, et al.
Pageof 59

Showing results (251-260 of 586) with videos related to

Sort By:
Pageof 59
Epilepsia|October 20, 2020
Fenfluramine HCl (Fintepla<sup>®</sup> ) provides long-term clinically meaningful reduction in seizure frequency: Analysis of an ongoing open-label extension studyJoseph Sullivan, Ingrid E Scheffer, Lieven Lagae, et al.
Neurology|August 30, 2019
Efficacy and tolerability of adjunctive lacosamide in pediatric patients with focal seizuresViktor Farkas, Barbara Steinborn, J Robert Flamini, et al.
Epilepsia|January 7, 2012
Clinical genetic studies in benign childhood epilepsy with centrotemporal spikesDanya F Vears, Meng-Han Tsai, Lynette G Sadleir, et al.
Frontiers in Neurology|April 1, 2022
Impaired Color Recognition in <i>HCN1</i> Epilepsy: A Single Case ReportChaseley E Mckenzie, Chen-Jui Ho, Ian C Forster, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 21, 2010
Detection of microchromosomal aberrations in refractory epilepsy: a pilot studyJacinta M McMahon, Ingrid E Scheffer, Jillian K Nicholl, et al.
European Journal of Human Genetics : EJHG|May 16, 2025
Understanding speech and language in KIF1A-associated neurological disorderLottie D Morison, Adam P Vogel, John Christodoulou, et al.
NAR Genomics and Bioinformatics|April 7, 2025
Identifying individuals with rare disease variants by inferring shared ancestral haplotypes from SNP array dataErandee Robertson, Bronwyn E Grinton, Karen L Oliver, et al.
The Lancet. Neurology|May 23, 2006
De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective studySamuel F Berkovic, Louise Harkin, Jacinta M McMahon, et al.
Translational Psychiatry|May 6, 2020
A standardized patient-centered characterization of the phenotypic spectrum of PCDH19 girls clustering epilepsyKristy L Kolc, Lynette G Sadleir, Christel Depienne, et al.
Epilepsia|November 18, 2020
Transcriptome analysis of a ring chromosome 20 patient cohortKenneth A Myers, Mark F Bennett, Michael S Hildebrand, et al.
Pageof 59