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Journal Abstract Search

682 related items for PubMed ID: 31537705

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  • 2. Sharp-Wave Ripple Frequency and Interictal Epileptic Discharges Increase in Tandem During Thermal Induction of Seizures in a Mouse Model of Genetic Epilepsy.
    Cheah CS, Beckman MA, Catterall WA, Oakley JC.
    Front Cell Neurosci; 2021; 15():751762. PubMed ID: 34733140
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  • 4. Strain- and age-dependent hippocampal neuron sodium currents correlate with epilepsy severity in Dravet syndrome mice.
    Mistry AM, Thompson CH, Miller AR, Vanoye CG, George AL, Kearney JA.
    Neurobiol Dis; 2014 May; 65():1-11. PubMed ID: 24434335
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  • 5. Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome.
    Rubinstein M, Westenbroek RE, Yu FH, Jones CJ, Scheuer T, Catterall WA.
    Neurobiol Dis; 2015 Jan; 73():106-17. PubMed ID: 25281316
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  • 8. Dissecting the phenotypes of Dravet syndrome by gene deletion.
    Rubinstein M, Han S, Tai C, Westenbroek RE, Hunker A, Scheuer T, Catterall WA.
    Brain; 2015 Aug; 138(Pt 8):2219-33. PubMed ID: 26017580
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  • 9. Ndnf Interneuron Excitability Is Spared in a Mouse Model of Dravet Syndrome.
    Liebergall SR, Goldberg EM.
    J Neurosci; 2024 Apr 24; 44(17):. PubMed ID: 38443186
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  • 10. Synaptic Integration in CA1 Pyramidal Neurons Is Intact despite Deficits in GABAergic Transmission in the Scn1a Haploinsufficiency Mouse Model of Dravet Syndrome.
    Chancey JH, Howard MA.
    eNeuro; 2022 Apr 24; 9(3):. PubMed ID: 35523580
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  • 11. Dravet Syndrome: A Developmental and Epileptic Encephalopathy.
    Lopez-Santiago L, Isom LL.
    Epilepsy Curr; 2019 Jan 24; 19(1):51-53. PubMed ID: 30838929
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  • 14. Targeted Augmentation of Nuclear Gene Output (TANGO) of Scn1a rescues parvalbumin interneuron excitability and reduces seizures in a mouse model of Dravet Syndrome.
    Wengert ER, Wagley PK, Strohm SM, Reza N, Wenker IC, Gaykema RP, Christiansen A, Liau G, Patel MK.
    Brain Res; 2022 Jan 15; 1775():147743. PubMed ID: 34843701
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  • 16. Functional and structural deficits of the dentate gyrus network coincide with emerging spontaneous seizures in an Scn1a mutant Dravet Syndrome model during development.
    Tsai MS, Lee ML, Chang CY, Fan HH, Yu IS, Chen YT, You JY, Chen CY, Chang FC, Hsiao JH, Khorkova O, Liou HH, Yanagawa Y, Lee LJ, Lin SW.
    Neurobiol Dis; 2015 May 15; 77():35-48. PubMed ID: 25725421
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  • 17. Interneuron Desynchronization Precedes Seizures in a Mouse Model of Dravet Syndrome.
    Tran CH, Vaiana M, Nakuci J, Somarowthu A, Goff KM, Goldstein N, Murthy P, Muldoon SF, Goldberg EM.
    J Neurosci; 2020 Mar 25; 40(13):2764-2775. PubMed ID: 32102923
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  • 18. Specific deletion of NaV1.1 sodium channels in inhibitory interneurons causes seizures and premature death in a mouse model of Dravet syndrome.
    Cheah CS, Yu FH, Westenbroek RE, Kalume FK, Oakley JC, Potter GB, Rubenstein JL, Catterall WA.
    Proc Natl Acad Sci U S A; 2012 Sep 04; 109(36):14646-51. PubMed ID: 22908258
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