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Ingo Helbig

Showing results (111-120 of 270) with videos related to

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Journal of Child Neurology|October 12, 2013
Atypical vitamin B6 deficiency: a rare cause of unexplained neonatal and infantile epilepsiesAnna Baumgart, Sarah von Spiczak, Nanda M Verhoeven-Duif, et al.
JAMA Network Open|April 13, 2019
Use of a Dynamic Genetic Testing Approach for Childhood-Onset EpilepsyJorune Balciuniene, Elizabeth T DeChene, Gozde Akgumus, et al.
Brain : a Journal of Neurology|March 17, 2022
Atypical development of Broca's area in a large family with inherited stutteringDaisy G Y Thompson-Lake, Thomas S Scerri, Susan Block, et al.
Epilepsia|April 26, 2008
Gene expression analysis in absence epilepsy using a monozygotic twin designIngo Helbig, Nicholas A Matigian, Lata Vadlamudi, et al.
The Neurohospitalist|April 13, 2022
Multicenter Study of the Impact of COVID-19 Shelter-In-Place on Tertiary Hospital-based Care for Pediatric Neurologic DiseaseMelissa L Hutchinson, Kendall B Nash, Nicholas S Abend, et al.
Molecular Genetics and Metabolism|July 25, 2022
Psychometric outcome measures in beta-propeller protein-associated neurodegeneration (BPAN)Francesco Gavazzi, Samuel R Pierce, Joseph Vithayathil, et al.
JCI Insight|February 1, 2022
High-throughput evaluation of epilepsy-associated KCNQ2 variants reveals functional and pharmacological heterogeneityCarlos G Vanoye, Reshma R Desai, Zhigang Ji, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 28, 2025
Rare variants in <i>BMAL1</i> are associated with a neurodevelopmental syndromeVishnu Anand Cuddapah, Dechun Chen, Bumsik Cho, et al.
Epilepsia|April 11, 2023
Review and standard operating procedures for collection of biospecimens and analysis of biomarkers in new onset refractory status epilepticusAurélie Hanin, Jorge Cespedes, Yashwanth Pulluru, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 7, 2019
Targeted gene sequencing in 6994 individuals with neurodevelopmental disorder with epilepsyHenrike O Heyne, Mykyta Artomov, Florian Battke, et al.
Pageof 27

Showing results (111-120 of 270) with videos related to

Sort By:
Pageof 27
Journal of Child Neurology|October 12, 2013
Atypical vitamin B6 deficiency: a rare cause of unexplained neonatal and infantile epilepsiesAnna Baumgart, Sarah von Spiczak, Nanda M Verhoeven-Duif, et al.
JAMA Network Open|April 13, 2019
Use of a Dynamic Genetic Testing Approach for Childhood-Onset EpilepsyJorune Balciuniene, Elizabeth T DeChene, Gozde Akgumus, et al.
Brain : a Journal of Neurology|March 17, 2022
Atypical development of Broca's area in a large family with inherited stutteringDaisy G Y Thompson-Lake, Thomas S Scerri, Susan Block, et al.
Epilepsia|April 26, 2008
Gene expression analysis in absence epilepsy using a monozygotic twin designIngo Helbig, Nicholas A Matigian, Lata Vadlamudi, et al.
The Neurohospitalist|April 13, 2022
Multicenter Study of the Impact of COVID-19 Shelter-In-Place on Tertiary Hospital-based Care for Pediatric Neurologic DiseaseMelissa L Hutchinson, Kendall B Nash, Nicholas S Abend, et al.
Molecular Genetics and Metabolism|July 25, 2022
Psychometric outcome measures in beta-propeller protein-associated neurodegeneration (BPAN)Francesco Gavazzi, Samuel R Pierce, Joseph Vithayathil, et al.
JCI Insight|February 1, 2022
High-throughput evaluation of epilepsy-associated KCNQ2 variants reveals functional and pharmacological heterogeneityCarlos G Vanoye, Reshma R Desai, Zhigang Ji, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 28, 2025
Rare variants in <i>BMAL1</i> are associated with a neurodevelopmental syndromeVishnu Anand Cuddapah, Dechun Chen, Bumsik Cho, et al.
Epilepsia|April 11, 2023
Review and standard operating procedures for collection of biospecimens and analysis of biomarkers in new onset refractory status epilepticusAurélie Hanin, Jorge Cespedes, Yashwanth Pulluru, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 7, 2019
Targeted gene sequencing in 6994 individuals with neurodevelopmental disorder with epilepsyHenrike O Heyne, Mykyta Artomov, Florian Battke, et al.
Pageof 27