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Ingrid E Scheffer

Showing results (161-170 of 586) with videos related to

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Epilepsy & Behavior : E&B|March 2, 2010
Neuropsychological function in patients with a single gene mutation associated with autosomal dominant nocturnal frontal lobe epilepsyAmanda G Wood, Michael M Saling, Marco Fedi, et al.
Plos One|January 21, 2018
KANSL1 variation is not a major contributing factor in self-limited focal epilepsy syndromes of childhoodKenneth A Myers, Amelia McGlade, Bernd A Neubauer, et al.
European Journal of Human Genetics : EJHG|August 9, 2022
Unexpected diagnosis of myotonic dystrophy type 2 repeat expansion by genome sequencingHaloom Rafehi, Cherie Green, Kiymet Bozaoglu, et al.
Developmental Medicine and Child Neurology|February 23, 2026
Developmental stuttering with common and complex phenotypesSarah E Horton, Daisy A Shepherd, Stephanie Siemers, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 14, 2020
Levetiracetam efficacy in PCDH19 Girls Clustering EpilepsyLynette G Sadleir, Kristy L Kolc, Chontelle King, et al.
Epilepsia|August 27, 2016
Hippocampal malrotation is an anatomic variant and has no clinical significance in MRI-negative temporal lobe epilepsyMeng-Han Tsai, David N Vaughan, Yuliya Perchyonok, et al.
Journal of Medical Genetics|March 8, 2013
Recent advances in the molecular genetics of epilepsyMichael S Hildebrand, Hans-Henrik M Dahl, John Anthony Damiano, et al.
Developmental Medicine and Child Neurology|June 15, 2013
Head stereotypies in STXBP1 encephalopathyYoung Ok Kim, Christian M Korff, Mel Michel G Villaluz, et al.
Developmental Medicine and Child Neurology|March 5, 2019
Perception of impact of Dravet syndrome on children and caregivers in multiple countries: looking beyond seizuresRima Nabbout, Stephane Auvin, Catherine Chiron, et al.
Epilepsy Research|April 19, 2017
Evaluation of GLUT1 variation in non-acquired focal epilepsyAlexander Peeraer, John A Damiano, Susannah T Bellows, et al.
Pageof 59

Showing results (161-170 of 586) with videos related to

Sort By:
Pageof 59
Epilepsy & Behavior : E&B|March 2, 2010
Neuropsychological function in patients with a single gene mutation associated with autosomal dominant nocturnal frontal lobe epilepsyAmanda G Wood, Michael M Saling, Marco Fedi, et al.
Plos One|January 21, 2018
KANSL1 variation is not a major contributing factor in self-limited focal epilepsy syndromes of childhoodKenneth A Myers, Amelia McGlade, Bernd A Neubauer, et al.
European Journal of Human Genetics : EJHG|August 9, 2022
Unexpected diagnosis of myotonic dystrophy type 2 repeat expansion by genome sequencingHaloom Rafehi, Cherie Green, Kiymet Bozaoglu, et al.
Developmental Medicine and Child Neurology|February 23, 2026
Developmental stuttering with common and complex phenotypesSarah E Horton, Daisy A Shepherd, Stephanie Siemers, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 14, 2020
Levetiracetam efficacy in PCDH19 Girls Clustering EpilepsyLynette G Sadleir, Kristy L Kolc, Chontelle King, et al.
Epilepsia|August 27, 2016
Hippocampal malrotation is an anatomic variant and has no clinical significance in MRI-negative temporal lobe epilepsyMeng-Han Tsai, David N Vaughan, Yuliya Perchyonok, et al.
Journal of Medical Genetics|March 8, 2013
Recent advances in the molecular genetics of epilepsyMichael S Hildebrand, Hans-Henrik M Dahl, John Anthony Damiano, et al.
Developmental Medicine and Child Neurology|June 15, 2013
Head stereotypies in STXBP1 encephalopathyYoung Ok Kim, Christian M Korff, Mel Michel G Villaluz, et al.
Developmental Medicine and Child Neurology|March 5, 2019
Perception of impact of Dravet syndrome on children and caregivers in multiple countries: looking beyond seizuresRima Nabbout, Stephane Auvin, Catherine Chiron, et al.
Epilepsy Research|April 19, 2017
Evaluation of GLUT1 variation in non-acquired focal epilepsyAlexander Peeraer, John A Damiano, Susannah T Bellows, et al.
Pageof 59