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Ingo Helbig

Showing results (61-70 of 292) with videos related to

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Epilepsy Research|April 21, 2018
Early mortality in SCN8A-related epilepsiesKatrine M Johannesen, Elena Gardella, Ingrid Scheffer, et al.
Developmental Medicine and Child Neurology|October 17, 2012
Febrile infection-related epilepsy syndrome (FIRES) is not caused by SCN1A, POLG, PCDH19 mutations or rare copy number variationsSilke Appenzeller, Ingo Helbig, Ulrich Stephani, et al.
Seminars in Pediatric Neurology|March 3, 2015
Status epilepticus and refractory status epilepticus managementNicholas S Abend, David Bearden, Ingo Helbig, et al.
Neuropediatrics|May 12, 2020
Whole-Exome Sequencing in NF1-Related West Syndrome Leads to the Identification of KCNC2 as a Novel Candidate Gene for EpilepsyAnnika Rademacher, Niklas Schwarz, Simone Seiffert, et al.
Neurology. Genetics|January 7, 2025
A Longitudinal Exploration of <i>CACNA1A</i>-Related Hemiplegic Migraine in Children Using Electronic Medical RecordsDonna Schaare, Laina Lusk, Alexis Karlin, et al.
Journal of Child Neurology|May 14, 2025
A Simple Intervention Improves Access to Telemedicine for Spanish-Speaking Families in an Outpatient Pediatric Epilepsy ClinicPamela Pojomovsky McDonnell, Yessenia Ortiz, Nicholas S Abend, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 23, 2016
Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsyKatherine L Helbig, Kelly D Farwell Hagman, Deepali N Shinde, et al.
Developmental Medicine and Child Neurology|April 11, 2026
Reliability and stability of cerebral palsy classification scales for individuals with STXBP1- and SYNGAP1-related disordersSamuel R Pierce, Julie M Orlando, Kristin G Cunningham, et al.
Epilepsy Research|March 26, 2013
Genetics of febrile seizure subtypes and syndromes: a twin studyJazmin Eckhaus, Kate M Lawrence, Ingo Helbig, et al.
Human Mutation|April 23, 2022
Computational analysis of neurodevelopmental phenotypes: Harmonization empowers clinical discoveryDavid Lewis-Smith, Shridhar Parthasarathy, Julie Xian, et al.
Pageof 30

Showing results (61-70 of 292) with videos related to

Sort By:
Pageof 30
Epilepsy Research|April 21, 2018
Early mortality in SCN8A-related epilepsiesKatrine M Johannesen, Elena Gardella, Ingrid Scheffer, et al.
Developmental Medicine and Child Neurology|October 17, 2012
Febrile infection-related epilepsy syndrome (FIRES) is not caused by SCN1A, POLG, PCDH19 mutations or rare copy number variationsSilke Appenzeller, Ingo Helbig, Ulrich Stephani, et al.
Seminars in Pediatric Neurology|March 3, 2015
Status epilepticus and refractory status epilepticus managementNicholas S Abend, David Bearden, Ingo Helbig, et al.
Neuropediatrics|May 12, 2020
Whole-Exome Sequencing in NF1-Related West Syndrome Leads to the Identification of KCNC2 as a Novel Candidate Gene for EpilepsyAnnika Rademacher, Niklas Schwarz, Simone Seiffert, et al.
Neurology. Genetics|January 7, 2025
A Longitudinal Exploration of <i>CACNA1A</i>-Related Hemiplegic Migraine in Children Using Electronic Medical RecordsDonna Schaare, Laina Lusk, Alexis Karlin, et al.
Journal of Child Neurology|May 14, 2025
A Simple Intervention Improves Access to Telemedicine for Spanish-Speaking Families in an Outpatient Pediatric Epilepsy ClinicPamela Pojomovsky McDonnell, Yessenia Ortiz, Nicholas S Abend, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 23, 2016
Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsyKatherine L Helbig, Kelly D Farwell Hagman, Deepali N Shinde, et al.
Developmental Medicine and Child Neurology|April 11, 2026
Reliability and stability of cerebral palsy classification scales for individuals with STXBP1- and SYNGAP1-related disordersSamuel R Pierce, Julie M Orlando, Kristin G Cunningham, et al.
Epilepsy Research|March 26, 2013
Genetics of febrile seizure subtypes and syndromes: a twin studyJazmin Eckhaus, Kate M Lawrence, Ingo Helbig, et al.
Human Mutation|April 23, 2022
Computational analysis of neurodevelopmental phenotypes: Harmonization empowers clinical discoveryDavid Lewis-Smith, Shridhar Parthasarathy, Julie Xian, et al.
Pageof 30