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Pediatrics
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March 24, 2017
Fatal Cerebral Edema With Status Epilepticus in Children With Dravet Syndrome: Report of 5 Cases
Kenneth A Myers, Jacinta M McMahon, Simone A Mandelstam, et al.
Epilepsia
|
January 19, 2017
Frequency of CNKSR2 mutation in the X-linked epilepsy-aphasia spectrum
John 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 Syndrome
Orrin Devinsky, J Helen Cross, Linda Laux, et al.
Epilepsia
|
April 10, 2013
Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies
Sarah 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 Study
Kenneth A Myers, Margot J Davey, Michael Ching, et al.
Neurology
|
February 16, 2021
Speech, Language, and Oromotor Skills in Patients With Polymicrogyria
Ruth 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 leukaemia
Ashalatha 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 dysarthria
Samantha 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 spectrum
Karl Martin Klein, Terence J O'Brien, Kavita Praveen, et al.
Page
of 59
Search research articles
Search
Showing results (191-200 of 586) with videos related to
Sort By:
Page
of 59
Pediatrics
|
March 24, 2017
Fatal Cerebral Edema With Status Epilepticus in Children With Dravet Syndrome: Report of 5 Cases
Kenneth A Myers, Jacinta M McMahon, Simone A Mandelstam, et al.
Epilepsia
|
January 19, 2017
Frequency of CNKSR2 mutation in the X-linked epilepsy-aphasia spectrum
John 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 Syndrome
Orrin Devinsky, J Helen Cross, Linda Laux, et al.
Epilepsia
|
April 10, 2013
Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies
Sarah 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 Study
Kenneth A Myers, Margot J Davey, Michael Ching, et al.
Neurology
|
February 16, 2021
Speech, Language, and Oromotor Skills in Patients With Polymicrogyria
Ruth 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 leukaemia
Ashalatha 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 dysarthria
Samantha 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 spectrum
Karl Martin Klein, Terence J O'Brien, Kavita Praveen, et al.
Page
of 59