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Non-synaptic Cell-Autonomous Mechanisms Underlie Neuronal Hyperactivity in a Genetic Model of PIK3CA -Driven Intractable Epilepsy.
- Published in:
- Frontiers in Molecular Neuroscience, 2021, v. 14, p. 1, doi. 10.3389/fnmol.2021.772847
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- Article
Reduced Sodium Current in Purkinje Neurons from Na<sub>V</sub>1.1 Mutant Mice: Implications for Ataxia in Severe Myoclonic Epilepsy in Infancy.
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- Journal of Neuroscience, 2007, v. 27, n. 41, p. 11065, doi. 10.1523/JNEUROSCI.2162-07.2007
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- Article
Molecular mimicry: Cross‐reactive antibodies from patients with immune‐mediated neurologic disease inhibit neuronal firing.
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- Journal of Neuroscience Research, 2004, v. 77, n. 1, p. 82, doi. 10.1002/jnr.20137
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- Article
ISDN2014_0157: Modeling human PIK3CA‐related congenital brain overgrowth and epilepsy in mice.
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- International Journal of Developmental Neuroscience, 2015, v. 47, p. 46, doi. 10.1016/j.ijdevneu.2015.04.131
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- Article
Mouse models of human PIK3CA-related brain overgrowth have acutely treatable epilepsy.
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- eLife, 2015, p. 1, doi. 10.7554/eLife.12703
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- Article
Na<sub>V</sub>1.1 channels and epilepsy.
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- Journal of Physiology, 2010, v. 588, n. 11, p. 1849, doi. 10.1113/jphysiol.2010.187484
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- Article
AUTS2 Regulates RNA Metabolism and Dentate Gyrus Development in Mice.
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- Cerebral Cortex, 2021, v. 31, n. 10, p. 4808, doi. 10.1093/cercor/bhab124
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- Article
Sudden unexpected death in a mouse model of Dravet syndrome.
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- Journal of Clinical Investigation, 2013, v. 123, n. 4, p. 1798, doi. 10.1172/JCI66220
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- Article
Autoimmunity due to molecular mimicry as a cause of neurological disease.
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- Nature Medicine, 2002, v. 8, n. 5, p. 509, doi. 10.1038/nm0502-509
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- Article
Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy.
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- 2007
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- Correction notice
Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy.
- Published in:
- Nature Neuroscience, 2006, v. 9, n. 9, p. 1142, doi. 10.1038/nn1754
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- Article
Protective effect of the ketogenic diet in Scn1a mutant mice.
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- Epilepsia (Series 4), 2011, v. 52, n. 11, p. 2050, doi. 10.1111/j.1528-1167.2011.03211.x
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- Article
Insights into pathophysiology and therapy from a mouse model of Dravet syndrome.
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- Epilepsia (Series 4), 2011, v. 52, p. 59, doi. 10.1111/j.1528-1167.2011.03004.x
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- Publication type:
- Article
Proceedings of the Sleep and Epilepsy Workshop: Section 3 Mortality: Sleep, Night, and SUDEP.
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- Epilepsy Currents, 2021, v. 21, n. 3, p. 215, doi. 10.1177/15357597211004556
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- Article