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Shakti Agrawal

Showing results (1-10 of 19) with videos related to

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Archives of Disease in Childhood. Education and Practice Edition|December 22, 2016
Management of children and young people with headacheWilliam P Whitehouse, Shakti Agrawal
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|November 11, 2020
Seizure improvement following vagus nerve stimulator (VNS) battery change with cardiac-based seizure detection automatic stimulation (AutoStim): early experience in a regional paediatric unitWilliam B Lo, Bethany Chevill, Sunny Philip, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 6, 2013
CLN6 disease caused by the same mutation originating in Pakistan has varying pathologyRita Guerreiro, Jose T Bras, Mariana Vieira, et al.
Archives of Disease in Childhood|February 1, 2015
N-methyl-D-aspartate receptor antibody-mediated neurological disease: results of a UK-based surveillance study in childrenSukhvir Wright, Yael Hacohen, Leslie Jacobson, et al.
American Journal of Medical Genetics. Part A|January 17, 2013
Striking intrafamilial phenotypic variability in Aicardi-Goutières syndrome associated with the recurrent Asian founder mutation in RNASEH2CJulie Vogt, Shakti Agrawal, Zala Ibrahim, et al.
Annals of Clinical and Translational Neurology|May 20, 2020
Abolishing spontaneous epileptiform activity in human brain tissue through AMPA receptor inhibitionSukhvir K Wright, Max A Wilson, Richard Walsh, et al.
Journal of Neurosurgery. Pediatrics|August 6, 2022
Functional hemispherotomy for epilepsy in the very youngJoshua Pepper, William B Lo, Shakti Agrawal, et al.
Epilepsy Research|August 16, 2024
The utility of Multicentre Epilepsy Lesion Detection (MELD) algorithm in identifying epileptic activity and predicting seizure freedom in MRI lesion-negative paediatric patientsAimee Goel, Stefano Seri, Shakti Agrawal, et al.
Annals of Neurology|July 31, 2015
Recessive ITPA mutations cause an early infantile encephalopathySietske H Kevelam, Jörgen Bierau, Ramona Salvarinova, et al.
Journal of Neurosurgery. Pediatrics|May 15, 2026
Can the 5-SENSE score guide stereo-electroencephalography in children? First validation in a purely pediatric cohortArnav S Singh, Stefano Seri, William B Lo, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

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Pageof 2
Archives of Disease in Childhood. Education and Practice Edition|December 22, 2016
Management of children and young people with headacheWilliam P Whitehouse, Shakti Agrawal
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|November 11, 2020
Seizure improvement following vagus nerve stimulator (VNS) battery change with cardiac-based seizure detection automatic stimulation (AutoStim): early experience in a regional paediatric unitWilliam B Lo, Bethany Chevill, Sunny Philip, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 6, 2013
CLN6 disease caused by the same mutation originating in Pakistan has varying pathologyRita Guerreiro, Jose T Bras, Mariana Vieira, et al.
Archives of Disease in Childhood|February 1, 2015
N-methyl-D-aspartate receptor antibody-mediated neurological disease: results of a UK-based surveillance study in childrenSukhvir Wright, Yael Hacohen, Leslie Jacobson, et al.
American Journal of Medical Genetics. Part A|January 17, 2013
Striking intrafamilial phenotypic variability in Aicardi-Goutières syndrome associated with the recurrent Asian founder mutation in RNASEH2CJulie Vogt, Shakti Agrawal, Zala Ibrahim, et al.
Annals of Clinical and Translational Neurology|May 20, 2020
Abolishing spontaneous epileptiform activity in human brain tissue through AMPA receptor inhibitionSukhvir K Wright, Max A Wilson, Richard Walsh, et al.
Journal of Neurosurgery. Pediatrics|August 6, 2022
Functional hemispherotomy for epilepsy in the very youngJoshua Pepper, William B Lo, Shakti Agrawal, et al.
Epilepsy Research|August 16, 2024
The utility of Multicentre Epilepsy Lesion Detection (MELD) algorithm in identifying epileptic activity and predicting seizure freedom in MRI lesion-negative paediatric patientsAimee Goel, Stefano Seri, Shakti Agrawal, et al.
Annals of Neurology|July 31, 2015
Recessive ITPA mutations cause an early infantile encephalopathySietske H Kevelam, Jörgen Bierau, Ramona Salvarinova, et al.
Journal of Neurosurgery. Pediatrics|May 15, 2026
Can the 5-SENSE score guide stereo-electroencephalography in children? First validation in a purely pediatric cohortArnav S Singh, Stefano Seri, William B Lo, et al.
Pageof 2