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Robyn Whitney

Showing results (41-50 of 99) with videos related to

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Neurology. Genetics|December 17, 2025
<i>DEGS1</i>-Related Hypomyelinating Leukodystrophy: Four Individuals From Same Family and Review of LiteratureMark Grinberg, Breanne Dale, Rajesh Ramachandrannair, et al.
Seizure|June 23, 2023
The genetic landscape of developmental and epileptic encephalopathy with spike-and-wave activation in sleepAlexander E Freibauer, Rajesh RamachandranNair, Puneet Jain, et al.
Genes|March 28, 2024
Genetic Advancements in Infantile Epileptic Spasms Syndrome and Opportunities for Precision MedicineHannah E Snyder, Puneet Jain, Rajesh RamachandranNair, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|June 17, 2018
Peri-oral myoclonia with absences with multiple facial and upper body myoclonia: Overlap epilepsy syndromePratima Gulati, Puneet Jain, Hebah Qashqari, et al.
Epilepsy Research|June 9, 2023
SUDEP: Living with the knowledgeRobyn Whitney, Sonya Strohm, Tamzin Jeffs, et al.
Neurology|June 10, 2018
Incidence of sudden unexpected death in epilepsy in children is similar to adultsAnne E Keller, Robyn Whitney, Shelly-Anne Li, et al.
Seizure|October 19, 2018
Perineal stimulation triggering seizures in a child with Dravet syndromePuneet Jain, Pratima Gulati, Daad Alsowat, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|December 27, 2023
Retrospective Analysis of Canadian Adults with Tuberous Sclerosis ComplexDominique Pal, Nicole Forster, Monika Madan, et al.
Epilepsy & Behavior : E&B|May 28, 2026
Navigating safety and sudden unexpected death in epilepsy (SUDEP) discussions in adolescents with epilepsy: short-term outcomes of a structured counselling interventionSachin Kumar, Aman Elwadhi, Sayoni Roy Chowdhury, et al.
Seizure|March 22, 2025
Biallelic SCN1A variants with divergent epilepsy phenotypesRowan Pentz, Rebecca Hough, Chumei Li, et al.
Pageof 10

Showing results (41-50 of 99) with videos related to

Sort By:
Pageof 10
Neurology. Genetics|December 17, 2025
<i>DEGS1</i>-Related Hypomyelinating Leukodystrophy: Four Individuals From Same Family and Review of LiteratureMark Grinberg, Breanne Dale, Rajesh Ramachandrannair, et al.
Seizure|June 23, 2023
The genetic landscape of developmental and epileptic encephalopathy with spike-and-wave activation in sleepAlexander E Freibauer, Rajesh RamachandranNair, Puneet Jain, et al.
Genes|March 28, 2024
Genetic Advancements in Infantile Epileptic Spasms Syndrome and Opportunities for Precision MedicineHannah E Snyder, Puneet Jain, Rajesh RamachandranNair, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|June 17, 2018
Peri-oral myoclonia with absences with multiple facial and upper body myoclonia: Overlap epilepsy syndromePratima Gulati, Puneet Jain, Hebah Qashqari, et al.
Epilepsy Research|June 9, 2023
SUDEP: Living with the knowledgeRobyn Whitney, Sonya Strohm, Tamzin Jeffs, et al.
Neurology|June 10, 2018
Incidence of sudden unexpected death in epilepsy in children is similar to adultsAnne E Keller, Robyn Whitney, Shelly-Anne Li, et al.
Seizure|October 19, 2018
Perineal stimulation triggering seizures in a child with Dravet syndromePuneet Jain, Pratima Gulati, Daad Alsowat, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|December 27, 2023
Retrospective Analysis of Canadian Adults with Tuberous Sclerosis ComplexDominique Pal, Nicole Forster, Monika Madan, et al.
Epilepsy & Behavior : E&B|May 28, 2026
Navigating safety and sudden unexpected death in epilepsy (SUDEP) discussions in adolescents with epilepsy: short-term outcomes of a structured counselling interventionSachin Kumar, Aman Elwadhi, Sayoni Roy Chowdhury, et al.
Seizure|March 22, 2025
Biallelic SCN1A variants with divergent epilepsy phenotypesRowan Pentz, Rebecca Hough, Chumei Li, et al.
Pageof 10