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Andrew Escayg

Showing results (51-60 of 60) with videos related to

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Pediatric Neurology|February 7, 2006
Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancyJennifer A Kearney, Anna K Wiste, Ulrich Stephani, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|March 4, 2021
Autistic-like behavior, spontaneous seizures, and increased neuronal excitability in a Scn8a mouse modelJennifer C Wong, Steven F Grieco, Karoni Dutt, et al.
The Journal of Biological Chemistry|January 27, 2010
Altered function of the SCN1A voltage-gated sodium channel leads to gamma-aminobutyric acid-ergic (GABAergic) interneuron abnormalitiesMelinda S Martin, Karoni Dutt, Ligia A Papale, et al.
Frontiers in Neurology|August 1, 2022
Novel Missense <i>CNTNAP2</i> Variant Identified in Two Consanguineous Pakistani Families With Developmental Delay, Epilepsy, Intellectual Disability, and Aggressive BehaviorNoor Badshah, Kari A Mattison, Sohail Ahmad, et al.
Neurobiology of Disease|July 10, 2017
GPR37L1 modulates seizure susceptibility: Evidence from mouse studies and analyses of a human GPR37L1 variantMichelle M Giddens, Jennifer C Wong, Jason P Schroeder, et al.
Cerebral Cortex (New York, N.Y. : 1991)|March 28, 2023
Mutations in plasticity-related-gene-1 (PRG-1) protein contribute to hippocampal seizure susceptibility and modify epileptic phenotypeEllen Knierim, Johannes Vogt, Michael Kintscher, et al.
Neurobiology of Disease|January 20, 2019
A two-hit story: Seizures and genetic mutation interaction sets phenotype severity in SCN1A epilepsiesAna Rita Salgueiro-Pereira, Fabrice Duprat, Paula A Pousinha, et al.
Biological Psychiatry|October 2, 2018
Noradrenergic Transmission at Alpha1-Adrenergic Receptors in the Ventral Periaqueductal Gray Modulates ArousalKirsten A Porter-Stransky, Samuel W Centanni, Saumya L Karne, et al.
Human Molecular Genetics|July 2, 2017
The RNA-binding protein, ZC3H14, is required for proper poly(A) tail length control, expression of synaptic proteins, and brain function in miceJennifer Rha, Stephanie K Jones, Jonathan Fidler, et al.
Brain : a Journal of Neurology|September 8, 2022
ATP6V0C variants impair V-ATPase function causing a neurodevelopmental disorder often associated with epilepsyKari A Mattison, Gilles Tossing, Fred Mulroe, et al.
Pageof 6

Showing results (51-60 of 60) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
Pediatric Neurology|February 7, 2006
Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancyJennifer A Kearney, Anna K Wiste, Ulrich Stephani, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|March 4, 2021
Autistic-like behavior, spontaneous seizures, and increased neuronal excitability in a Scn8a mouse modelJennifer C Wong, Steven F Grieco, Karoni Dutt, et al.
The Journal of Biological Chemistry|January 27, 2010
Altered function of the SCN1A voltage-gated sodium channel leads to gamma-aminobutyric acid-ergic (GABAergic) interneuron abnormalitiesMelinda S Martin, Karoni Dutt, Ligia A Papale, et al.
Frontiers in Neurology|August 1, 2022
Novel Missense <i>CNTNAP2</i> Variant Identified in Two Consanguineous Pakistani Families With Developmental Delay, Epilepsy, Intellectual Disability, and Aggressive BehaviorNoor Badshah, Kari A Mattison, Sohail Ahmad, et al.
Neurobiology of Disease|July 10, 2017
GPR37L1 modulates seizure susceptibility: Evidence from mouse studies and analyses of a human GPR37L1 variantMichelle M Giddens, Jennifer C Wong, Jason P Schroeder, et al.
Cerebral Cortex (New York, N.Y. : 1991)|March 28, 2023
Mutations in plasticity-related-gene-1 (PRG-1) protein contribute to hippocampal seizure susceptibility and modify epileptic phenotypeEllen Knierim, Johannes Vogt, Michael Kintscher, et al.
Neurobiology of Disease|January 20, 2019
A two-hit story: Seizures and genetic mutation interaction sets phenotype severity in SCN1A epilepsiesAna Rita Salgueiro-Pereira, Fabrice Duprat, Paula A Pousinha, et al.
Biological Psychiatry|October 2, 2018
Noradrenergic Transmission at Alpha1-Adrenergic Receptors in the Ventral Periaqueductal Gray Modulates ArousalKirsten A Porter-Stransky, Samuel W Centanni, Saumya L Karne, et al.
Human Molecular Genetics|July 2, 2017
The RNA-binding protein, ZC3H14, is required for proper poly(A) tail length control, expression of synaptic proteins, and brain function in miceJennifer Rha, Stephanie K Jones, Jonathan Fidler, et al.
Brain : a Journal of Neurology|September 8, 2022
ATP6V0C variants impair V-ATPase function causing a neurodevelopmental disorder often associated with epilepsyKari A Mattison, Gilles Tossing, Fred Mulroe, et al.
Pageof 6