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Proceedings of the National Academy of Sciences of the United States of America
|
February 18, 2021
The zebrafish <i>grime</i> mutant uncovers an evolutionarily conserved role for Tmem161b in the control of cardiac rhythm
Charlotte D Koopman, Jessica De Angelis, Swati P Iyer, et al.
Epilepsia
|
February 5, 2026
Mechanisms of SCN2A loss of function do not predict presence or phenotype of epilepsy
Marsha Tan, Beatrice Southby Goad, Meagan Allen, et al.
American Journal of Human Genetics
|
April 14, 2015
Mutations in the GABA Transporter SLC6A1 Cause Epilepsy with Myoclonic-Atonic Seizures
Gemma L Carvill, Jacinta M McMahon, Amy Schneider, et al.
Human Molecular Genetics
|
July 19, 2015
A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis
Ben J Gu, Judith Field, Sébastien Dutertre, et al.
Annals of Clinical and Translational Neurology
|
September 5, 2015
PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy
Michael S Hildebrand, Rick Tankard, Elena V Gazina, et al.
BMC Cancer
|
December 2, 2025
Pharmacological targeting and characterization of Voltage-Gated Sodium Channels (VGSCs) expressed in the high-grade glioma microenvironment
Emily V Fletcher, Chloe Shard, Yasmin Boyle, et al.
Neurology
|
December 3, 2017
Clinical and molecular characterization of <i>KCNT1</i>-related severe early-onset epilepsy
Amy McTague, Umesh Nair, Sony Malhotra, et al.
Trends in Neurosciences
|
April 26, 2018
Progress in Understanding and Treating SCN2A-Mediated Disorders
Stephan J Sanders, Arthur J Campbell, Jeffrey R Cottrell, et al.
Circulation
|
July 15, 2021
Therapeutic Inhibition of Acid-Sensing Ion Channel 1a Recovers Heart Function After Ischemia-Reperfusion Injury
Meredith A Redd, Sarah E Scheuer, Natalie J Saez, et al.
Annals of Neurology
|
April 6, 2017
Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K<sup>+</sup> channel properties
Karen L Oliver, Silvana Franceschetti, Carol J Milligan, et al.
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of 19
Search research articles
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Showing results (171-180 of 182) with videos related to
Sort By:
Page
of 19
Proceedings of the National Academy of Sciences of the United States of America
|
February 18, 2021
The zebrafish <i>grime</i> mutant uncovers an evolutionarily conserved role for Tmem161b in the control of cardiac rhythm
Charlotte D Koopman, Jessica De Angelis, Swati P Iyer, et al.
Epilepsia
|
February 5, 2026
Mechanisms of SCN2A loss of function do not predict presence or phenotype of epilepsy
Marsha Tan, Beatrice Southby Goad, Meagan Allen, et al.
American Journal of Human Genetics
|
April 14, 2015
Mutations in the GABA Transporter SLC6A1 Cause Epilepsy with Myoclonic-Atonic Seizures
Gemma L Carvill, Jacinta M McMahon, Amy Schneider, et al.
Human Molecular Genetics
|
July 19, 2015
A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis
Ben J Gu, Judith Field, Sébastien Dutertre, et al.
Annals of Clinical and Translational Neurology
|
September 5, 2015
PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy
Michael S Hildebrand, Rick Tankard, Elena V Gazina, et al.
BMC Cancer
|
December 2, 2025
Pharmacological targeting and characterization of Voltage-Gated Sodium Channels (VGSCs) expressed in the high-grade glioma microenvironment
Emily V Fletcher, Chloe Shard, Yasmin Boyle, et al.
Neurology
|
December 3, 2017
Clinical and molecular characterization of <i>KCNT1</i>-related severe early-onset epilepsy
Amy McTague, Umesh Nair, Sony Malhotra, et al.
Trends in Neurosciences
|
April 26, 2018
Progress in Understanding and Treating SCN2A-Mediated Disorders
Stephan J Sanders, Arthur J Campbell, Jeffrey R Cottrell, et al.
Circulation
|
July 15, 2021
Therapeutic Inhibition of Acid-Sensing Ion Channel 1a Recovers Heart Function After Ischemia-Reperfusion Injury
Meredith A Redd, Sarah E Scheuer, Natalie J Saez, et al.
Annals of Neurology
|
April 6, 2017
Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K<sup>+</sup> channel properties
Karen L Oliver, Silvana Franceschetti, Carol J Milligan, et al.
Page
of 19