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Ingrid E Scheffer

Showing results (191-200 of 586) with videos related to

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Pediatrics|March 24, 2017
Fatal Cerebral Edema With Status Epilepticus in Children With Dravet Syndrome: Report of 5 CasesKenneth A Myers, Jacinta M McMahon, Simone A Mandelstam, et al.
Epilepsia|January 19, 2017
Frequency of CNKSR2 mutation in the X-linked epilepsy-aphasia spectrumJohn A Damiano, Rosemary Burgess, Sara Kivity, et al.
The New England Journal of Medicine|May 25, 2017
Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet SyndromeOrrin Devinsky, J Helen Cross, Linda Laux, et al.
Epilepsia|April 10, 2013
Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathiesSarah E Heron, Yeh Sze Ong, Simone C Yendle, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|October 25, 2018
Randomized Controlled Trial of Melatonin for Sleep Disturbance in Dravet Syndrome: The DREAMS StudyKenneth A Myers, Margot J Davey, Michael Ching, et al.
Neurology|February 16, 2021
Speech, Language, and Oromotor Skills in Patients With PolymicrogyriaRuth O Braden, Jessica O Boyce, Chloe A Stutterd, et al.
Neuroimage|February 9, 2010
Focal epileptiform spikes do not show a canonical BOLD response in patients with benign rolandic epilepsy (BECTS)Richard A J Masterton, A Simon Harvey, John S Archer, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|November 20, 2008
Multifocal epilepsy: the role of palliative resection - intractable frontal and occipital lobe epilepsy secondary to radiotherapy for acute lymphoblastic leukaemiaAshalatha Radhakrishnan, Pasiri Sithinamsuwan, A Simon Harvey, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthriaSamantha J Turner, Michael S Hildebrand, Susan Block, et al.
Epilepsia|July 12, 2012
Familial focal epilepsy with variable foci mapped to chromosome 22q12: expansion of the phenotypic spectrumKarl Martin Klein, Terence J O'Brien, Kavita Praveen, et al.
Pageof 59

Showing results (191-200 of 586) with videos related to

Sort By:
Pageof 59
Pediatrics|March 24, 2017
Fatal Cerebral Edema With Status Epilepticus in Children With Dravet Syndrome: Report of 5 CasesKenneth A Myers, Jacinta M McMahon, Simone A Mandelstam, et al.
Epilepsia|January 19, 2017
Frequency of CNKSR2 mutation in the X-linked epilepsy-aphasia spectrumJohn A Damiano, Rosemary Burgess, Sara Kivity, et al.
The New England Journal of Medicine|May 25, 2017
Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet SyndromeOrrin Devinsky, J Helen Cross, Linda Laux, et al.
Epilepsia|April 10, 2013
Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathiesSarah E Heron, Yeh Sze Ong, Simone C Yendle, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|October 25, 2018
Randomized Controlled Trial of Melatonin for Sleep Disturbance in Dravet Syndrome: The DREAMS StudyKenneth A Myers, Margot J Davey, Michael Ching, et al.
Neurology|February 16, 2021
Speech, Language, and Oromotor Skills in Patients With PolymicrogyriaRuth O Braden, Jessica O Boyce, Chloe A Stutterd, et al.
Neuroimage|February 9, 2010
Focal epileptiform spikes do not show a canonical BOLD response in patients with benign rolandic epilepsy (BECTS)Richard A J Masterton, A Simon Harvey, John S Archer, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|November 20, 2008
Multifocal epilepsy: the role of palliative resection - intractable frontal and occipital lobe epilepsy secondary to radiotherapy for acute lymphoblastic leukaemiaAshalatha Radhakrishnan, Pasiri Sithinamsuwan, A Simon Harvey, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthriaSamantha J Turner, Michael S Hildebrand, Susan Block, et al.
Epilepsia|July 12, 2012
Familial focal epilepsy with variable foci mapped to chromosome 22q12: expansion of the phenotypic spectrumKarl Martin Klein, Terence J O'Brien, Kavita Praveen, et al.
Pageof 59