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Ingrid E Scheffer

Showing results (201-210 of 586) with videos related to

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Epilepsia|April 14, 2010
Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3Sarah E Heron, Ingrid E Scheffer, Bronwyn E Grinton, et al.
Developmental Medicine and Child Neurology|June 16, 2020
Focal epilepsy in SCN1A-mutation carrying patients: is there a role for epilepsy surgery?Aikaterini Vezyroglou, Sophia Varadkar, Thomas Bast, et al.
Journal of Child Neurology|March 24, 2022
Focal Epilepsy in Children With Tuberous Sclerosis Complex: Does Vigabatrin Control Focal Seizures?Sufang Lin, Jianxiang Liao, Xia Zhao, et al.
Epilepsia|July 23, 2011
Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypesJohn C Mulley, Ingrid E Scheffer, Tarishi Desai, et al.
Epilepsia|June 7, 2018
Heart rate variability in epilepsy: A potential biomarker of sudden unexpected death in epilepsy riskKenneth A Myers, Luis E Bello-Espinosa, Joseph D Symonds, et al.
Epilepsy Research|July 12, 2019
Somatic mutation: The hidden genetics of brain malformations and focal epilepsiesZimeng Ye, Lara McQuillan, Annapurna Poduri, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 7, 2025
Fulfilling the needs of caregivers in delivering health services to children with developmental and epileptic encephalopathiesLauren Kelada, Stephanie Best, Kristine Pierce, et al.
Epilepsia|May 5, 2026
Disrupted inhibitory interneuron development in SCN1A Dravet syndrome revealed by patient-derived subpallial organoidsCristiana Mattei, Miaomiao Mao, Sean Byars, et al.
Epilepsia|December 24, 2011
Long-term follow-up of febrile infection-related epilepsy syndromeKatherine B Howell, Kamornwan Katanyuwong, Mark T Mackay, et al.
Epilepsia Open|May 25, 2021
Seizures in Sotos syndrome: Phenotyping in 49 patientsOlivier Fortin, Christian Vincelette, Afsheen Q Khan, et al.
Pageof 59

Showing results (201-210 of 586) with videos related to

Sort By:
Pageof 59
Epilepsia|April 14, 2010
Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3Sarah E Heron, Ingrid E Scheffer, Bronwyn E Grinton, et al.
Developmental Medicine and Child Neurology|June 16, 2020
Focal epilepsy in SCN1A-mutation carrying patients: is there a role for epilepsy surgery?Aikaterini Vezyroglou, Sophia Varadkar, Thomas Bast, et al.
Journal of Child Neurology|March 24, 2022
Focal Epilepsy in Children With Tuberous Sclerosis Complex: Does Vigabatrin Control Focal Seizures?Sufang Lin, Jianxiang Liao, Xia Zhao, et al.
Epilepsia|July 23, 2011
Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypesJohn C Mulley, Ingrid E Scheffer, Tarishi Desai, et al.
Epilepsia|June 7, 2018
Heart rate variability in epilepsy: A potential biomarker of sudden unexpected death in epilepsy riskKenneth A Myers, Luis E Bello-Espinosa, Joseph D Symonds, et al.
Epilepsy Research|July 12, 2019
Somatic mutation: The hidden genetics of brain malformations and focal epilepsiesZimeng Ye, Lara McQuillan, Annapurna Poduri, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 7, 2025
Fulfilling the needs of caregivers in delivering health services to children with developmental and epileptic encephalopathiesLauren Kelada, Stephanie Best, Kristine Pierce, et al.
Epilepsia|May 5, 2026
Disrupted inhibitory interneuron development in SCN1A Dravet syndrome revealed by patient-derived subpallial organoidsCristiana Mattei, Miaomiao Mao, Sean Byars, et al.
Epilepsia|December 24, 2011
Long-term follow-up of febrile infection-related epilepsy syndromeKatherine B Howell, Kamornwan Katanyuwong, Mark T Mackay, et al.
Epilepsia Open|May 25, 2021
Seizures in Sotos syndrome: Phenotyping in 49 patientsOlivier Fortin, Christian Vincelette, Afsheen Q Khan, et al.
Pageof 59