| scholarly article | Q13442814 |
| P2093 | author name string | Dominique M Durand | |
| Nan Tian | |||
| Kara Buehrer Kile | |||
| P2860 | cites work | Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2 | Q22253421 |
| Radicals r'aging | Q24322096 | ||
| De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy | Q24533495 | ||
| Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus. | Q24536353 | ||
| A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy | Q24536363 | ||
| A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction | Q24626279 | ||
| Sodium-channel defects in benign familial neonatal-infantile seizures | Q28202961 | ||
| Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures | Q28207332 | ||
| Nav1.1 mutations cause febrile seizures associated with afebrile partial seizures | Q28214517 | ||
| Theta oscillations in the hippocampus | Q28217796 | ||
| Quantitative evaluation of neuronal loss in the dorsal hippocampus in rats with long-term pilocarpine seizures | Q28243959 | ||
| A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline | Q28251184 | ||
| Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy | Q28253135 | ||
| International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels | Q28289125 | ||
| Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancy | Q28295604 | ||
| Initiation of network bursts by Ca2+-dependent intrinsic bursting in the rat pilocarpine model of temporal lobe epilepsy | Q28361757 | ||
| Interaction between the sodium channel inactivation linker and domain III S4-S5. | Q33907560 | ||
| Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy | Q34122789 | ||
| Generalized epilepsy with febrile seizures plus: mutation of the sodium channel subunit SCN1B. | Q34128513 | ||
| Complications associated with genetic background effects in models of experimental epilepsy | Q34763771 | ||
| Cellular mechanisms of neuronal population oscillations in the hippocampus in vitro. | Q35817070 | ||
| Cellular and molecular mechanisms of epilepsy in the human brain | Q36322311 | ||
| Methodological approaches to exploring epileptic disorders in the human brain in vitro | Q36497165 | ||
| Isolated brain slices. A new preparation for theoretical and clinical research | Q40314213 | ||
| De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy | Q40558873 | ||
| Generalized epilepsy with febrile seizures plus: further heterogeneity in a large family | Q40595241 | ||
| Cellular electrophysiology of human epilepsy | Q40662472 | ||
| Ictal patterns in experimental models of epilepsy | Q40863627 | ||
| Long-duration self-sustained epileptiform activity in the hippocampal-parahippocampal slice: a model of status epilepticus | Q40967199 | ||
| Brainstem-diencephalo-septohippocampal systems controlling the theta rhythm of the hippocampus. | Q41611896 | ||
| Local circuit synaptic interactions in hippocampal brain slices | Q41636996 | ||
| Impaired electrical signaling disrupts gamma frequency oscillations in connexin 36-deficient mice | Q43715220 | ||
| Interictal high-frequency oscillations (80-500 Hz) in the human epileptic brain: entorhinal cortex | Q44153747 | ||
| Anticonvulsant actions of gap junctional blockers in an in vitro seizure model. | Q44168253 | ||
| High-frequency oscillations after status epilepticus: epileptogenesis and seizure genesis | Q45030225 | ||
| Generation and propagation of epileptiform discharges in a combined entorhinal cortex/hippocampal slice | Q45091412 | ||
| Circuit mechanisms of seizures in the pilocarpine model of chronic epilepsy: cell loss and mossy fiber sprouting. | Q45999480 | ||
| Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2. | Q46933257 | ||
| Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy | Q47756691 | ||
| Electrical coupling underlies high-frequency oscillations in the hippocampus in vitro | Q47908475 | ||
| Plaque-associated disruption of CSF and plasma amyloid-beta (Abeta) equilibrium in a mouse model of Alzheimer's disease | Q48579999 | ||
| Modulation of endogenous firing patterns by osmolarity in rat hippocampal neurones | Q48669658 | ||
| Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B. | Q48934070 | ||
| A gain-of-function mutation in the sodium channel gene Scn2a results in seizures and behavioral abnormalities | Q49049294 | ||
| Nonfunctional SCN1A is common in severe myoclonic epilepsy of infancy. | Q53592417 | ||
| Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients. | Q54590725 | ||
| Genetic modifiers affecting severity of epilepsy caused by mutation of sodium channel Scn2a. | Q54634416 | ||
| Animal models of the epilepsies | Q69548740 | ||
| Altered brain sodium channel transcript levels in human epilepsy | Q71284236 | ||
| Endogenous bursting due to altered sodium channel function in rat hippocampal CA1 neurons | Q72033012 | ||
| Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancy | Q74361012 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 3 | |
| P304 | page(s) | 488-499 | |
| P577 | publication date | 2007-11-21 | |
| P1433 | published in | Epilepsia | Q5382969 |
| P1476 | title | Scn2a sodium channel mutation results in hyperexcitability in the hippocampus in vitro | |
| P478 | volume | 49 |
| Q35762766 | Autism spectrum disorder and epilepsy: Disorders with a shared biology |
| Q42219555 | CaMKII modulates sodium current in neurons from epileptic Scn2a mutant mice |
| Q38418209 | Enhanced in vitro CA1 network activity in a sodium channel β1(C121W) subunit model of genetic epilepsy. |
| Q30535330 | Low frequency stimulation decreases seizure activity in a mutation model of epilepsy. |
| Q36598428 | Low frequency stimulation of ventral hippocampal commissures reduces seizures in a rat model of chronic temporal lobe epilepsy |
| Q28293955 | SCN2A mutation is associated with infantile spasms and bitemporal glucose hypometabolism |
Search more.