Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Ingrid E Scheffer

Showing results (291-300 of 586) with videos related to

Pageof 59
Sort By:
Epilepsia|August 5, 2025
Is there really evidence for neurodegeneration in Dravet syndrome? Commentary on the publication by Selvarajah et alSanjay M Sisodiya, Simona Balestrini, Samuel F Berkovic, et al.
International Journal of Molecular Sciences|October 30, 2020
Tracing Autism Traits in Large Multiplex Families to Identify Endophenotypes of the Broader Autism PhenotypeKrysta J Trevis, Natasha J Brown, Cherie C Green, et al.
Neuron|January 5, 2018
Abnormal Cell Sorting Underlies the Unique X-Linked Inheritance of PCDH19 EpilepsyDaniel T Pederick, Kay L Richards, Sandra G Piltz, et al.
Annals of Neurology|May 4, 2010
Augmented currents of an HCN2 variant in patients with febrile seizure syndromesLeanne M Dibbens, Christopher A Reid, Bree Hodgson, et al.
American Journal of Human Genetics|December 19, 2001
Truncation of the GABA(A)-receptor gamma2 subunit in a family with generalized epilepsy with febrile seizures plusLouise A Harkin, David N Bowser, Leanne M Dibbens, et al.
Neurology. Genetics|August 12, 2024
Inherited <i>PURA</i> Pathogenic Variant Associated With a Mild Neurodevelopmental DisorderMichael S Hildebrand, Ruth O Braden, Mariana L Lauretta, et al.
Developmental Medicine and Child Neurology|July 11, 2021
Genetic convergence of developmental and epileptic encephalopathies and intellectual disabilityGemma L Carvill, Sandra Jansen, Amy Lacroix, et al.
Annals of Neurology|January 3, 2013
Glucose transporter 1 deficiency in the idiopathic generalized epilepsiesTodor Arsov, Saul A Mullen, Sue Rogers, et al.
Epilepsia|March 13, 2020
Inherited RORB pathogenic variants: Overlap of photosensitive genetic generalized and occipital lobe epilepsyLynette G Sadleir, Guillem de Valles-Ibáñez, Chontelle King, et al.
Annals of Neurology|July 7, 2017
Familial mesial temporal lobe epilepsy and the borderland of déjà vuPiero Perucca, Douglas E Crompton, Susannah T Bellows, et al.
Pageof 59

Showing results (291-300 of 586) with videos related to

Sort By:
Pageof 59
Epilepsia|August 5, 2025
Is there really evidence for neurodegeneration in Dravet syndrome? Commentary on the publication by Selvarajah et alSanjay M Sisodiya, Simona Balestrini, Samuel F Berkovic, et al.
International Journal of Molecular Sciences|October 30, 2020
Tracing Autism Traits in Large Multiplex Families to Identify Endophenotypes of the Broader Autism PhenotypeKrysta J Trevis, Natasha J Brown, Cherie C Green, et al.
Neuron|January 5, 2018
Abnormal Cell Sorting Underlies the Unique X-Linked Inheritance of PCDH19 EpilepsyDaniel T Pederick, Kay L Richards, Sandra G Piltz, et al.
Annals of Neurology|May 4, 2010
Augmented currents of an HCN2 variant in patients with febrile seizure syndromesLeanne M Dibbens, Christopher A Reid, Bree Hodgson, et al.
American Journal of Human Genetics|December 19, 2001
Truncation of the GABA(A)-receptor gamma2 subunit in a family with generalized epilepsy with febrile seizures plusLouise A Harkin, David N Bowser, Leanne M Dibbens, et al.
Neurology. Genetics|August 12, 2024
Inherited <i>PURA</i> Pathogenic Variant Associated With a Mild Neurodevelopmental DisorderMichael S Hildebrand, Ruth O Braden, Mariana L Lauretta, et al.
Developmental Medicine and Child Neurology|July 11, 2021
Genetic convergence of developmental and epileptic encephalopathies and intellectual disabilityGemma L Carvill, Sandra Jansen, Amy Lacroix, et al.
Annals of Neurology|January 3, 2013
Glucose transporter 1 deficiency in the idiopathic generalized epilepsiesTodor Arsov, Saul A Mullen, Sue Rogers, et al.
Epilepsia|March 13, 2020
Inherited RORB pathogenic variants: Overlap of photosensitive genetic generalized and occipital lobe epilepsyLynette G Sadleir, Guillem de Valles-Ibáñez, Chontelle King, et al.
Annals of Neurology|July 7, 2017
Familial mesial temporal lobe epilepsy and the borderland of déjà vuPiero Perucca, Douglas E Crompton, Susannah T Bellows, et al.
Pageof 59