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Alfred L George

Showing results (91-100 of 296) with videos related to

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The Journal of Physiology|October 8, 2005
Sodium channel dysfunction in intractable childhood epilepsy with generalized tonic-clonic seizuresThomas H Rhodes, Carlos G Vanoye, Iori Ohmori, et al.
Neurobiology of Disease|October 26, 2013
Novel SCN3A variants associated with focal epilepsy in childrenCarlos G Vanoye, Christina A Gurnett, Katherine D Holland, et al.
Epilepsia Open|November 18, 2025
Neurodevelopmental features in KCNQ2 developmental and epileptic encephalopathy may have limited associations with K<sub>V</sub>7.2 dysfunctionJessa S Bidwell, Carlos G Vanoye, Reshma R Desai, et al.
Scientific Reports|May 12, 2017
Unexpected Efficacy of a Novel Sodium Channel Modulator in Dravet SyndromeLyndsey L Anderson, Nicole A Hawkins, Christopher H Thompson, et al.
Annals of Clinical and Translational Neurology|September 28, 2019
Functional consequences of a KCNT1 variant associated with status dystonicus and early-onset infantile encephalopathyTracy S Gertler, Christopher H Thompson, Carlos G Vanoye, et al.
Plos Computational Biology|April 20, 2022
Predicting the functional impact of KCNQ1 variants with artificial neural networksSaksham Phul, Georg Kuenze, Carlos G Vanoye, et al.
Plos One|October 8, 2011
Transcriptional networks in epithelial-mesenchymal transitionChristo Venkov, David Plieth, Terri Ni, et al.
Journal of Cardiovascular Electrophysiology|April 11, 2002
Polymorphisms in beta-adrenergic receptor genes in the acquired long QT syndromeHideaki Kanki, Ping Yang, Hong-Guang Xie, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2026
Combining automated patch clamp with optogenetics enables selective recording of DRG neurons subtypesCarlos G Vanoye, Dongjun Ren, Abdelhak Belmadani, et al.
Channels (Austin, Tex.)|February 15, 2011
Ranolazine block of human Na v 1.4 sodium channels and paramyotonia congenita mutantsNesrine El-Bizri, Kristopher M Kahlig, John C Shyrock, et al.
Pageof 30

Showing results (91-100 of 296) with videos related to

Sort By:
Pageof 30
The Journal of Physiology|October 8, 2005
Sodium channel dysfunction in intractable childhood epilepsy with generalized tonic-clonic seizuresThomas H Rhodes, Carlos G Vanoye, Iori Ohmori, et al.
Neurobiology of Disease|October 26, 2013
Novel SCN3A variants associated with focal epilepsy in childrenCarlos G Vanoye, Christina A Gurnett, Katherine D Holland, et al.
Epilepsia Open|November 18, 2025
Neurodevelopmental features in KCNQ2 developmental and epileptic encephalopathy may have limited associations with K<sub>V</sub>7.2 dysfunctionJessa S Bidwell, Carlos G Vanoye, Reshma R Desai, et al.
Scientific Reports|May 12, 2017
Unexpected Efficacy of a Novel Sodium Channel Modulator in Dravet SyndromeLyndsey L Anderson, Nicole A Hawkins, Christopher H Thompson, et al.
Annals of Clinical and Translational Neurology|September 28, 2019
Functional consequences of a KCNT1 variant associated with status dystonicus and early-onset infantile encephalopathyTracy S Gertler, Christopher H Thompson, Carlos G Vanoye, et al.
Plos Computational Biology|April 20, 2022
Predicting the functional impact of KCNQ1 variants with artificial neural networksSaksham Phul, Georg Kuenze, Carlos G Vanoye, et al.
Plos One|October 8, 2011
Transcriptional networks in epithelial-mesenchymal transitionChristo Venkov, David Plieth, Terri Ni, et al.
Journal of Cardiovascular Electrophysiology|April 11, 2002
Polymorphisms in beta-adrenergic receptor genes in the acquired long QT syndromeHideaki Kanki, Ping Yang, Hong-Guang Xie, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2026
Combining automated patch clamp with optogenetics enables selective recording of DRG neurons subtypesCarlos G Vanoye, Dongjun Ren, Abdelhak Belmadani, et al.
Channels (Austin, Tex.)|February 15, 2011
Ranolazine block of human Na v 1.4 sodium channels and paramyotonia congenita mutantsNesrine El-Bizri, Kristopher M Kahlig, John C Shyrock, et al.
Pageof 30