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International Journal of Molecular Sciences
|
July 13, 2019
Epileptic Encephalopathy In A Patient With A Novel Variant In The Kv7.2 S2 Transmembrane Segment: Clinical, Genetic, and Functional Features
Maria Virginia Soldovieri, Paolo Ambrosino, Ilaria Mosca, et al.
Experimental Neurology
|
June 12, 2022
Removal of KCNQ2 from parvalbumin-expressing interneurons improves anti-seizure efficacy of retigabine
Junzhan Jing, Corrinne Dunbar, Alina Sonesra, et al.
Nature Neuroscience
|
November 3, 2014
Glial ankyrins facilitate paranodal axoglial junction assembly
Kae-Jiun Chang, Daniel R Zollinger, Keiichiro Susuki, et al.
Epilepsia
|
November 19, 2016
Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain-of-function variant
John J Millichap, Francesco Miceli, Michela De Maria, et al.
Annals of Clinical and Translational Neurology
|
February 16, 2023
KCNA1 gain-of-function epileptic encephalopathy treated with 4-aminopyridine
Peter Müller, Danielle S Takacs, Ulrike B S Hedrich, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
January 19, 2024
Phenotypic and functional assessment of two novel KCNQ2 gain-of-function variants Y141N and G239S and effects of amitriptyline treatment
Allan Bayat, Stefano Iavarone, Francesco Miceli, et al.
Plos One
|
March 24, 2015
Ion channel expression in the developing enteric nervous system
Caroline S Hirst, Jaime P P Foong, Lincon A Stamp, et al.
Frontiers in Physiology
|
October 5, 2020
A Novel Kv7.3 Variant in the Voltage-Sensing S<sub>4</sub> Segment in a Family With Benign Neonatal Epilepsy: Functional Characterization and <i>in vitro</i> Rescue by β-Hydroxybutyrate
Francesco Miceli, Lidia Carotenuto, Vincenzo Barrese, et al.
JCI Insight
|
February 1, 2022
High-throughput evaluation of epilepsy-associated KCNQ2 variants reveals functional and pharmacological heterogeneity
Carlos G Vanoye, Reshma R Desai, Zhigang Ji, et al.
Epilepsia
|
February 1, 2017
Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain-of-function variants R201C and R201H
Sarah B Mulkey, Bruria Ben-Zeev, Joost Nicolai, et al.
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Search research articles
Search
Showing results (21-30 of 35) with videos related to
Sort By:
Page
of 4
International Journal of Molecular Sciences
|
July 13, 2019
Epileptic Encephalopathy In A Patient With A Novel Variant In The Kv7.2 S2 Transmembrane Segment: Clinical, Genetic, and Functional Features
Maria Virginia Soldovieri, Paolo Ambrosino, Ilaria Mosca, et al.
Experimental Neurology
|
June 12, 2022
Removal of KCNQ2 from parvalbumin-expressing interneurons improves anti-seizure efficacy of retigabine
Junzhan Jing, Corrinne Dunbar, Alina Sonesra, et al.
Nature Neuroscience
|
November 3, 2014
Glial ankyrins facilitate paranodal axoglial junction assembly
Kae-Jiun Chang, Daniel R Zollinger, Keiichiro Susuki, et al.
Epilepsia
|
November 19, 2016
Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain-of-function variant
John J Millichap, Francesco Miceli, Michela De Maria, et al.
Annals of Clinical and Translational Neurology
|
February 16, 2023
KCNA1 gain-of-function epileptic encephalopathy treated with 4-aminopyridine
Peter Müller, Danielle S Takacs, Ulrike B S Hedrich, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
January 19, 2024
Phenotypic and functional assessment of two novel KCNQ2 gain-of-function variants Y141N and G239S and effects of amitriptyline treatment
Allan Bayat, Stefano Iavarone, Francesco Miceli, et al.
Plos One
|
March 24, 2015
Ion channel expression in the developing enteric nervous system
Caroline S Hirst, Jaime P P Foong, Lincon A Stamp, et al.
Frontiers in Physiology
|
October 5, 2020
A Novel Kv7.3 Variant in the Voltage-Sensing S<sub>4</sub> Segment in a Family With Benign Neonatal Epilepsy: Functional Characterization and <i>in vitro</i> Rescue by β-Hydroxybutyrate
Francesco Miceli, Lidia Carotenuto, Vincenzo Barrese, et al.
JCI Insight
|
February 1, 2022
High-throughput evaluation of epilepsy-associated KCNQ2 variants reveals functional and pharmacological heterogeneity
Carlos G Vanoye, Reshma R Desai, Zhigang Ji, et al.
Epilepsia
|
February 1, 2017
Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain-of-function variants R201C and R201H
Sarah B Mulkey, Bruria Ben-Zeev, Joost Nicolai, et al.
Page
of 4