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Molecular basis of an inherited epilepsy
scientific article (publication date: 13 June 2002)
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scholarly article
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title
Molecular basis of an inherited epilepsy
(English)
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author
Christoph Lossin
series ordinal
1
object named as
Christoph Lossin
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author name string
Dao W Wang
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2
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Thomas H Rhodes
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3
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Carlos G Vanoye
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4
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Alfred L George
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5
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language of work or name
English
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publication date
13 June 2002
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published in
Neuron
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volume
34
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page(s)
877-84
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issue
6
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cites work
Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation
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A sodium channel mutation causing epilepsy in man exhibits subtle defects in fast inactivation and activation in vitro
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Enhanced inactivation and acceleration of activation of the sodium channel associated with epilepsy in man
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Excitability changes and inhibitory mechanisms in neocortical neurons during seizures.
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First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene
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Molecular mechanism for an inherited cardiac arrhythmia
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Epilepsy
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Spectrum of sodium channel disturbances in the nondystrophic myotonias and periodic paralyses
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Theoretical reconstruction of myotonia and paralysis caused by incomplete inactivation of sodium channels
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Cellular and molecular biology of voltage-gated sodium channels
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De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy
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'Non-synaptic' mechanisms in seizures and epileptogenesis
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Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2
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A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy
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Nomenclature of voltage-gated sodium channels
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Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches
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Nonsynaptic modulation of neuronal activity in the brain: electric currents and extracellular ions
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Inactivation of cloned Na channels expressed in Xenopus oocytes
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CORTICAL CELLULAR PHENOMENA IN EXPERIMENTAL EPILEPSY: ICTAL MANIFESTATIONS.
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On the cellular and network bases of epileptic seizures.
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Identification of epilepsy genes in human and mouse
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Fast and slow gating of sodium channels encoded by a single mRNA.
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Electrophysiological characterization of Na+ currents in acutely isolated human hippocampal dentate granule cells
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Human fetal central neurons in culture: voltage- and ligand-gated currents
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Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes
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Epileptiform activity in microcultures containing one excitatory hippocampal neuron.
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Endogenous bursts underlie seizurelike activity in solitary excitatory hippocampal neurons in microcultures.
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Mechanism of epilepsy
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Generalized epilepsy with febrile seizures plus: A common childhood-onset genetic epilepsy syndrome
1 reference
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Functional effects of two voltage-gated sodium channel mutations that cause generalized epilepsy with febrile seizures plus type 2
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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
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Radicals r'aging
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Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures
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Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus.
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Identifiers
DOI
10.1016/S0896-6273(02)00714-6
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PubMed ID
12086636
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ResearchGate publication ID
11288149
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