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Danielle M Andrade

Showing results (61-70 of 122) with videos related to

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Neurology(R) Neuroimmunology & Neuroinflammation|October 8, 2015
GRIN1 polymorphisms do not affect susceptibility or phenotype in NMDA receptor encephalitisGregory S Day, Harald Prüss, Susanne M Benseler, et al.
Epilepsy & Behavior : E&B|July 25, 2025
Genetic Epilepsies: Clinical pearls for early career epileptologistsDanielle 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 migrationArezoo Rezazadeh, Eduard Bercovici, Tim-Rasmus Kiehl, et al.
Epilepsia|July 6, 2019
Clinical utility of multigene panel testing in adults with epilepsy and intellectual disabilityFelippe 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 TargetVibhor Krishna, Nicolas Kon Kam King, Francesco Sammartino, et al.
Seizure|March 29, 2014
Deep brain stimulation for the management of seizures in MECP2 duplication syndromeFabio 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 unitSonia Poochikian-Sarkissian, Peter Tai, Martin del Campo, et al.
Neurology. Genetics|July 20, 2016
Progressive myoclonus epilepsy associated with SACS gene mutationsFábio A Nascimento, Laura Canafoglia, Danah Aljaafari, et al.
Epilepsia|April 28, 2017
22q11.2 deletion syndrome lowers seizure threshold in adult patients without epilepsyRobert G Wither, Felippe Borlot, Alex MacDonald, et al.
Pageof 13

Showing results (61-70 of 122) with videos related to

Sort By:
Pageof 13
Neurology(R) Neuroimmunology & Neuroinflammation|October 8, 2015
GRIN1 polymorphisms do not affect susceptibility or phenotype in NMDA receptor encephalitisGregory S Day, Harald Prüss, Susanne M Benseler, et al.
Epilepsy & Behavior : E&B|July 25, 2025
Genetic Epilepsies: Clinical pearls for early career epileptologistsDanielle 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 migrationArezoo Rezazadeh, Eduard Bercovici, Tim-Rasmus Kiehl, et al.
Epilepsia|July 6, 2019
Clinical utility of multigene panel testing in adults with epilepsy and intellectual disabilityFelippe 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 TargetVibhor Krishna, Nicolas Kon Kam King, Francesco Sammartino, et al.
Seizure|March 29, 2014
Deep brain stimulation for the management of seizures in MECP2 duplication syndromeFabio 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 unitSonia Poochikian-Sarkissian, Peter Tai, Martin del Campo, et al.
Neurology. Genetics|July 20, 2016
Progressive myoclonus epilepsy associated with SACS gene mutationsFábio A Nascimento, Laura Canafoglia, Danah Aljaafari, et al.
Epilepsia|April 28, 2017
22q11.2 deletion syndrome lowers seizure threshold in adult patients without epilepsyRobert G Wither, Felippe Borlot, Alex MacDonald, et al.
Pageof 13