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Epilepsy & Behavior Reports
|
July 28, 2022
Predictors of longitudinal seizure outcomes after epilepsy surgery in childhood
Amy Ka, Amir Taher, Stephanie D'Souza, et al.
Developmental Medicine and Child Neurology
|
June 10, 2021
Severe speech impairment is a distinguishing feature of FOXP1-related disorder
Ruth O Braden, David J Amor, Simon E Fisher, et al.
Neurology. Genetics
|
December 25, 2019
Yield of comparative genomic hybridization microarray in pediatric neurology practice
Shibalik Misra, Greg Peters, Elizabeth Barnes, et al.
Developmental Medicine and Child Neurology
|
December 24, 2019
BRAT1 encephalopathy: a recessive cause of epilepsy of infancy with migrating focal seizures
Ingrid E Scheffer, Katja E Boysen, Amy L Schneider, et al.
Neurophysiologie Clinique = Clinical Neurophysiology
|
December 7, 2024
The development of Stereo-Electroencephalography (SEEG) in Southeast Asia and Oceania: Challenges to equity across the region
Michael W K Fong, Kheng-Seang Lim, Si Lei Fong, et al.
Epilepsy Research
|
March 6, 2012
Febrile infection-related epilepsy syndrome is not caused by SCN1A mutations
Daniel Carranza Rojo, A Simon Harvey, Xenia Iona, et al.
Seizure
|
June 1, 2018
Diagnostic yield of targeted massively parallel sequencing in children with epileptic encephalopathy
Kavitha Kothur, Katherine Holman, Elizabeth Farnsworth, et al.
Epilepsy Research
|
November 5, 2016
Mortality in Dravet syndrome
Monica S Cooper, Anne Mcintosh, Douglas E Crompton, et al.
Neurology
|
August 11, 2017
Not all <i>SCN1A</i> epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotype
Lynette G Sadleir, Emily I Mountier, Deepak Gill, et al.
Annals of Clinical and Translational Neurology
|
June 21, 2023
CSF neopterin and quinolinic acid are biomarkers of neuroinflammation and neurotoxicity in FIRES and other infection-triggered encephalopathy syndromes
Russell C Dale, Terrence Thomas, Shrujna Patel, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 97) with videos related to
Sort By:
Page
of 10
Epilepsy & Behavior Reports
|
July 28, 2022
Predictors of longitudinal seizure outcomes after epilepsy surgery in childhood
Amy Ka, Amir Taher, Stephanie D'Souza, et al.
Developmental Medicine and Child Neurology
|
June 10, 2021
Severe speech impairment is a distinguishing feature of FOXP1-related disorder
Ruth O Braden, David J Amor, Simon E Fisher, et al.
Neurology. Genetics
|
December 25, 2019
Yield of comparative genomic hybridization microarray in pediatric neurology practice
Shibalik Misra, Greg Peters, Elizabeth Barnes, et al.
Developmental Medicine and Child Neurology
|
December 24, 2019
BRAT1 encephalopathy: a recessive cause of epilepsy of infancy with migrating focal seizures
Ingrid E Scheffer, Katja E Boysen, Amy L Schneider, et al.
Neurophysiologie Clinique = Clinical Neurophysiology
|
December 7, 2024
The development of Stereo-Electroencephalography (SEEG) in Southeast Asia and Oceania: Challenges to equity across the region
Michael W K Fong, Kheng-Seang Lim, Si Lei Fong, et al.
Epilepsy Research
|
March 6, 2012
Febrile infection-related epilepsy syndrome is not caused by SCN1A mutations
Daniel Carranza Rojo, A Simon Harvey, Xenia Iona, et al.
Seizure
|
June 1, 2018
Diagnostic yield of targeted massively parallel sequencing in children with epileptic encephalopathy
Kavitha Kothur, Katherine Holman, Elizabeth Farnsworth, et al.
Epilepsy Research
|
November 5, 2016
Mortality in Dravet syndrome
Monica S Cooper, Anne Mcintosh, Douglas E Crompton, et al.
Neurology
|
August 11, 2017
Not all <i>SCN1A</i> epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotype
Lynette G Sadleir, Emily I Mountier, Deepak Gill, et al.
Annals of Clinical and Translational Neurology
|
June 21, 2023
CSF neopterin and quinolinic acid are biomarkers of neuroinflammation and neurotoxicity in FIRES and other infection-triggered encephalopathy syndromes
Russell C Dale, Terrence Thomas, Shrujna Patel, et al.
Page
of 10