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Neurology(R) Neuroimmunology & Neuroinflammation
|
October 8, 2015
GRIN1 polymorphisms do not affect susceptibility or phenotype in NMDA receptor encephalitis
Gregory S Day, Harald Prüss, Susanne M Benseler, et al.
Epilepsy & Behavior : E&B
|
July 25, 2025
Genetic Epilepsies: Clinical pearls for early career epileptologists
Danielle M Andrade, Victor S T Lira, Farah Qaiser, et al.
Genes
|
February 25, 2023
Excluding Digenic Inheritance of <i>PGAP2</i> and <i>PGAP3</i> Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with <i>PGAP2</i> Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3)
Miles D Thompson, Xueying Li, Michele Spencer-Manzon, et al.
Annals of Clinical and Translational Neurology
|
November 28, 2018
Periventricular nodular heterotopia in 22q11.2 deletion and frontal lobe migration
Arezoo Rezazadeh, Eduard Bercovici, Tim-Rasmus Kiehl, et al.
Epilepsia
|
July 6, 2019
Clinical utility of multigene panel testing in adults with epilepsy and intellectual disability
Felippe Borlot, Bruno Ivo de Almeida, Shari L Combe, et al.
Neurosurgery
|
January 28, 2016
Anterior Nucleus Deep Brain Stimulation for Refractory Epilepsy: Insights Into Patterns of Seizure Control and Efficacious Target
Vibhor Krishna, Nicolas Kon Kam King, Francesco Sammartino, et al.
Seizure
|
March 29, 2014
Deep brain stimulation for the management of seizures in MECP2 duplication syndrome
Fabio A Nascimento, Hanna Faghfoury, Timo Krings, et al.
Canadian Journal of Neuroscience Nursing
|
January 21, 2010
Patient awareness of seizures as documented in the epilepsy monitoring unit
Sonia Poochikian-Sarkissian, Peter Tai, Martin del Campo, et al.
Neurology. Genetics
|
July 20, 2016
Progressive myoclonus epilepsy associated with SACS gene mutations
Fábio A Nascimento, Laura Canafoglia, Danah Aljaafari, et al.
Epilepsia
|
April 28, 2017
22q11.2 deletion syndrome lowers seizure threshold in adult patients without epilepsy
Robert G Wither, Felippe Borlot, Alex MacDonald, et al.
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of 13
Search research articles
Search
Showing results (61-70 of 122) with videos related to
Sort By:
Page
of 13
Neurology(R) Neuroimmunology & Neuroinflammation
|
October 8, 2015
GRIN1 polymorphisms do not affect susceptibility or phenotype in NMDA receptor encephalitis
Gregory S Day, Harald Prüss, Susanne M Benseler, et al.
Epilepsy & Behavior : E&B
|
July 25, 2025
Genetic Epilepsies: Clinical pearls for early career epileptologists
Danielle M Andrade, Victor S T Lira, Farah Qaiser, et al.
Genes
|
February 25, 2023
Excluding Digenic Inheritance of <i>PGAP2</i> and <i>PGAP3</i> Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with <i>PGAP2</i> Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3)
Miles D Thompson, Xueying Li, Michele Spencer-Manzon, et al.
Annals of Clinical and Translational Neurology
|
November 28, 2018
Periventricular nodular heterotopia in 22q11.2 deletion and frontal lobe migration
Arezoo Rezazadeh, Eduard Bercovici, Tim-Rasmus Kiehl, et al.
Epilepsia
|
July 6, 2019
Clinical utility of multigene panel testing in adults with epilepsy and intellectual disability
Felippe Borlot, Bruno Ivo de Almeida, Shari L Combe, et al.
Neurosurgery
|
January 28, 2016
Anterior Nucleus Deep Brain Stimulation for Refractory Epilepsy: Insights Into Patterns of Seizure Control and Efficacious Target
Vibhor Krishna, Nicolas Kon Kam King, Francesco Sammartino, et al.
Seizure
|
March 29, 2014
Deep brain stimulation for the management of seizures in MECP2 duplication syndrome
Fabio A Nascimento, Hanna Faghfoury, Timo Krings, et al.
Canadian Journal of Neuroscience Nursing
|
January 21, 2010
Patient awareness of seizures as documented in the epilepsy monitoring unit
Sonia Poochikian-Sarkissian, Peter Tai, Martin del Campo, et al.
Neurology. Genetics
|
July 20, 2016
Progressive myoclonus epilepsy associated with SACS gene mutations
Fábio A Nascimento, Laura Canafoglia, Danah Aljaafari, et al.
Epilepsia
|
April 28, 2017
22q11.2 deletion syndrome lowers seizure threshold in adult patients without epilepsy
Robert G Wither, Felippe Borlot, Alex MacDonald, et al.
Page
of 13