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Ingrid E Scheffer

Showing results (131-140 of 586) with videos related to

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Epilepsia|February 22, 2023
Genes4Epilepsy: An epilepsy gene resourceKaren L Oliver, Ingrid E Scheffer, Mark F Bennett, et al.
Brain : a Journal of Neurology|December 13, 2002
Childhood absence epilepsy and febrile seizures: a family with a GABA(A) receptor mutationCarla Marini, Louise A Harkin, Robyn H Wallace, et al.
Ebiomedicine|October 30, 2024
Investigating the effect of polygenic background on epilepsy phenotype in 'monogenic' familiesKaren L Oliver, Ingrid E Scheffer, Colin A Ellis, et al.
Journal of Paediatrics and Child Health|September 2, 2022
Response to sequential treatment with prednisolone and vigabatrin in infantile spasmsWinston Dzau, Sally Cheng, Penny Snell, et al.
Folia Phoniatrica Et Logopaedica : Official Organ of the International Association of Logopedics and Phoniatrics (IALP)|July 23, 2019
Looking to the Future: Speech, Language, and Academic Outcomes in an Adolescent with Childhood Apraxia of SpeechSamantha J Turner, Adam P Vogel, Bronwyn Parry-Fielder, et al.
Human Mutation|May 10, 2005
SCN1A mutations and epilepsyJohn C Mulley, Ingrid E Scheffer, Steven Petrou, et al.
Epilepsia|July 12, 2008
Factors influencing clinical features of absence seizuresLynette G Sadleir, Ingrid E Scheffer, Sherry Smith, et al.
Nature Reviews. Disease Primers|May 4, 2018
EpilepsyOrrin Devinsky, Annamaria Vezzani, Terence J O'Brien, et al.
Annals of Neurology|December 27, 2016
ReplyKatherine L Helbig, Ulrike B S Hedrich, Ingrid E Scheffer, et al.
Neurology|January 18, 2015
GRIN2A: an aptly named gene for speech dysfunctionSamantha J Turner, Angela K Mayes, Andrea Verhoeven, et al.
Pageof 59

Showing results (131-140 of 586) with videos related to

Sort By:
Pageof 59
Epilepsia|February 22, 2023
Genes4Epilepsy: An epilepsy gene resourceKaren L Oliver, Ingrid E Scheffer, Mark F Bennett, et al.
Brain : a Journal of Neurology|December 13, 2002
Childhood absence epilepsy and febrile seizures: a family with a GABA(A) receptor mutationCarla Marini, Louise A Harkin, Robyn H Wallace, et al.
Ebiomedicine|October 30, 2024
Investigating the effect of polygenic background on epilepsy phenotype in 'monogenic' familiesKaren L Oliver, Ingrid E Scheffer, Colin A Ellis, et al.
Journal of Paediatrics and Child Health|September 2, 2022
Response to sequential treatment with prednisolone and vigabatrin in infantile spasmsWinston Dzau, Sally Cheng, Penny Snell, et al.
Folia Phoniatrica Et Logopaedica : Official Organ of the International Association of Logopedics and Phoniatrics (IALP)|July 23, 2019
Looking to the Future: Speech, Language, and Academic Outcomes in an Adolescent with Childhood Apraxia of SpeechSamantha J Turner, Adam P Vogel, Bronwyn Parry-Fielder, et al.
Human Mutation|May 10, 2005
SCN1A mutations and epilepsyJohn C Mulley, Ingrid E Scheffer, Steven Petrou, et al.
Epilepsia|July 12, 2008
Factors influencing clinical features of absence seizuresLynette G Sadleir, Ingrid E Scheffer, Sherry Smith, et al.
Nature Reviews. Disease Primers|May 4, 2018
EpilepsyOrrin Devinsky, Annamaria Vezzani, Terence J O'Brien, et al.
Annals of Neurology|December 27, 2016
ReplyKatherine L Helbig, Ulrike B S Hedrich, Ingrid E Scheffer, et al.
Neurology|January 18, 2015
GRIN2A: an aptly named gene for speech dysfunctionSamantha J Turner, Angela K Mayes, Andrea Verhoeven, et al.
Pageof 59