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Alexander Rotenberg

Showing results (181-190 of 208) with videos related to

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Annals of Neurology|November 8, 2024
Enhancement of Glutamate Uptake as Novel Antiseizure Approach: Preclinical Proof of ConceptKrzysztof Kamiński, Katarzyna Socała, Michał Abram, et al.
Biological Psychiatry|March 4, 2019
Electrophysiological Phenotype in Angelman Syndrome Differs Between GenotypesJoel Frohlich, Meghan T Miller, Lynne M Bird, et al.
Annals of Neurology|April 3, 2019
Recurrent SLC1A2 variants cause epilepsy via a dominant negative mechanismAndrew B Stergachis, Jonai Pujol-Giménez, Gergely Gyimesi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 21, 2021
A pathogenic UFSP2 variant in an autosomal recessive form of pediatric neurodevelopmental anomalies and epilepsyMin Ni, Bushra Afroze, Chao Xing, et al.
Epilepsia|July 30, 2014
Safety and retention rate of rufinamide in 300 patients: a single pediatric epilepsy center experienceSigride Thome-Souza, Navah E Kadish, Sriram Ramgopal, et al.
Molecular Psychiatry|February 14, 2025
Phenotypic rescue via mTOR inhibition in neuron-specific Pten knockout mice reveals AKT and mTORC1-site specific changesAngelica D'Amore, Maria Sundberg, Rui Lin, et al.
Brain Stimulation|April 15, 2020
Early transcranial direct current stimulation treatment exerts neuroprotective effects on 6-OHDA-induced Parkinsonism in ratsXiao-Jun Feng, Yu-Ting Huang, Ying-Zu Huang, et al.
Epilepsia|March 24, 2023
The presence and severity of epilepsy coincide with reduced γ-aminobutyrate and cortical excitatory markers in succinic semialdehyde dehydrogenase deficiencyItay Tokatly Latzer, Mariarita Bertoldi, Melissa L DiBacco, et al.
Molecular Genetics and Metabolism|February 7, 2025
The neuropsychological profile of SSADH deficiency, a neurotransmitter disorder of GABA metabolismItay Tokatly Latzer, Ellen Hanson, Mariarita Bertoldi, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2026
<i>FMR1</i> reduction alters cellular and circuit properties in human cortexAditi Singh, Saman Abbaspoor, Leeyup Chung, et al.
Pageof 21

Showing results (181-190 of 208) with videos related to

Sort By:
Pageof 21
Annals of Neurology|November 8, 2024
Enhancement of Glutamate Uptake as Novel Antiseizure Approach: Preclinical Proof of ConceptKrzysztof Kamiński, Katarzyna Socała, Michał Abram, et al.
Biological Psychiatry|March 4, 2019
Electrophysiological Phenotype in Angelman Syndrome Differs Between GenotypesJoel Frohlich, Meghan T Miller, Lynne M Bird, et al.
Annals of Neurology|April 3, 2019
Recurrent SLC1A2 variants cause epilepsy via a dominant negative mechanismAndrew B Stergachis, Jonai Pujol-Giménez, Gergely Gyimesi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 21, 2021
A pathogenic UFSP2 variant in an autosomal recessive form of pediatric neurodevelopmental anomalies and epilepsyMin Ni, Bushra Afroze, Chao Xing, et al.
Epilepsia|July 30, 2014
Safety and retention rate of rufinamide in 300 patients: a single pediatric epilepsy center experienceSigride Thome-Souza, Navah E Kadish, Sriram Ramgopal, et al.
Molecular Psychiatry|February 14, 2025
Phenotypic rescue via mTOR inhibition in neuron-specific Pten knockout mice reveals AKT and mTORC1-site specific changesAngelica D'Amore, Maria Sundberg, Rui Lin, et al.
Brain Stimulation|April 15, 2020
Early transcranial direct current stimulation treatment exerts neuroprotective effects on 6-OHDA-induced Parkinsonism in ratsXiao-Jun Feng, Yu-Ting Huang, Ying-Zu Huang, et al.
Epilepsia|March 24, 2023
The presence and severity of epilepsy coincide with reduced γ-aminobutyrate and cortical excitatory markers in succinic semialdehyde dehydrogenase deficiencyItay Tokatly Latzer, Mariarita Bertoldi, Melissa L DiBacco, et al.
Molecular Genetics and Metabolism|February 7, 2025
The neuropsychological profile of SSADH deficiency, a neurotransmitter disorder of GABA metabolismItay Tokatly Latzer, Ellen Hanson, Mariarita Bertoldi, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2026
<i>FMR1</i> reduction alters cellular and circuit properties in human cortexAditi Singh, Saman Abbaspoor, Leeyup Chung, et al.
Pageof 21