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Cyrus Boelman

Showing results (1-10 of 35) with videos related to

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Genes|December 23, 2023
<i>STXBP1</i>-Related Disorders: Clinical Presentation, Molecular Function, Treatment, and Future DirectionsAlexander Freibauer, Mikayla Wohlleben, Cyrus Boelman
American Journal of Medical Genetics. Part A|January 24, 2024
Epilepsy in Legius syndrome: Coincidence or causation?Adalbeis Medina Lemus, Cyrus Boelman, Kenneth A Myers
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 5, 2020
Rapid Implementation of Virtual Health in a Pediatric Neurology Practice During COVID-19James Lee, Dewi Schrader, Cyrus Boelman, et al.
Oxford Medical Case Reports|October 17, 2024
Rhythmic high-amplitude delta with superimposed spikes (RHADS): a treatment dilemmaVanita Shukla, Paul Webb, Bashayer AlMohaimeed, et al.
BMC Medical Genetics|June 2, 2019
Case reports: novel TUBG1 mutations with milder neurodevelopmental presentationsYue T K Yuen, Ilaria Guella, Elke Roland, et al.
Epilepsia|July 30, 2014
Preictal surrender of post-spike slow waves to spike-related high-frequency oscillations (80-200 Hz) is associated with seizure initiationYosuke Sato, Sam M Doesburg, Simeon M Wong, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 16, 2019
EEG of asymptomatic first-degree relatives of patients with juvenile myoclonic, childhood absence and rolandic epilepsy: a systematic review and meta-analysisMariam Tashkandi, Duaa Baarma, Andrea C Tricco, et al.
Journal of Child Neurology|May 18, 2017
Clinical Experience With Perampanel for Refractory Pediatric Epilepsy in One Canadian CenterAnita N Datta, Qi Xu, Shafina Sachedina, et al.
Neuroimage|July 26, 2003
Statistical mapping analysis of lesion location and neurological disability in multiple sclerosis: application to 452 patient data setsArnaud Charil, Alex P Zijdenbos, Jonathan Taylor, et al.
Pediatric Neurology|December 3, 2014
Identical ATP1A3 mutation causes alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism phenotypesCyrus Boelman, Ana Marissa Lagman-Bartolome, Daune L MacGregor, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Genes|December 23, 2023
<i>STXBP1</i>-Related Disorders: Clinical Presentation, Molecular Function, Treatment, and Future DirectionsAlexander Freibauer, Mikayla Wohlleben, Cyrus Boelman
American Journal of Medical Genetics. Part A|January 24, 2024
Epilepsy in Legius syndrome: Coincidence or causation?Adalbeis Medina Lemus, Cyrus Boelman, Kenneth A Myers
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 5, 2020
Rapid Implementation of Virtual Health in a Pediatric Neurology Practice During COVID-19James Lee, Dewi Schrader, Cyrus Boelman, et al.
Oxford Medical Case Reports|October 17, 2024
Rhythmic high-amplitude delta with superimposed spikes (RHADS): a treatment dilemmaVanita Shukla, Paul Webb, Bashayer AlMohaimeed, et al.
BMC Medical Genetics|June 2, 2019
Case reports: novel TUBG1 mutations with milder neurodevelopmental presentationsYue T K Yuen, Ilaria Guella, Elke Roland, et al.
Epilepsia|July 30, 2014
Preictal surrender of post-spike slow waves to spike-related high-frequency oscillations (80-200 Hz) is associated with seizure initiationYosuke Sato, Sam M Doesburg, Simeon M Wong, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 16, 2019
EEG of asymptomatic first-degree relatives of patients with juvenile myoclonic, childhood absence and rolandic epilepsy: a systematic review and meta-analysisMariam Tashkandi, Duaa Baarma, Andrea C Tricco, et al.
Journal of Child Neurology|May 18, 2017
Clinical Experience With Perampanel for Refractory Pediatric Epilepsy in One Canadian CenterAnita N Datta, Qi Xu, Shafina Sachedina, et al.
Neuroimage|July 26, 2003
Statistical mapping analysis of lesion location and neurological disability in multiple sclerosis: application to 452 patient data setsArnaud Charil, Alex P Zijdenbos, Jonathan Taylor, et al.
Pediatric Neurology|December 3, 2014
Identical ATP1A3 mutation causes alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism phenotypesCyrus Boelman, Ana Marissa Lagman-Bartolome, Daune L MacGregor, et al.
Pageof 4