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Are some idiopathic epilepsies disorders of ion channels?: A working hypothesis.
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1 reference
stated in
Europe PubMed Central
PubMed publication ID
10962210
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10962210%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
review article
1 reference
stated in
Europe PubMed Central
title
Are some idiopathic epilepsies disorders of ion channels?: A working hypothesis
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10962210
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10962210%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
author
Shinichi Hirose
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10962210
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10962210%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
Motohiro Okada
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10962210
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10962210%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
author name string
S Kaneko
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10962210
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10962210%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
A Mitsudome
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10962210
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10962210%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
publication date
1 October 2000
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10962210
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10962210%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
published in
Epilepsy Research
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10962210
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10962210%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
volume
41
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10962210
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10962210%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10962210
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10962210%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
page(s)
191-204
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10962210
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10962210%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
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MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia
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A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33.
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Properties of neuronal nicotinic acetylcholine receptor mutants from humans suffering from autosomal dominant nocturnal frontal lobe epilepsy
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7 January 2021
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A potassium channel mutation in neonatal human epilepsy
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7 January 2021
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Structural and mutational analysis of KCNQ2, the major gene locus for benign familial neonatal convulsions
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7 January 2021
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M-currents: an update
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Identification of two new KCNA1 mutations in episodic ataxia/myokymia families
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7 January 2021
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Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
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7 January 2021
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Early-onset epilepsy and postnatal lethality associated with an editing-deficient GluR-B allele in mice
1 reference
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Crossref
reference URL
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7 January 2021
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Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
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7 January 2021
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The pilocarpine model of epilepsy in mice
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Crossref
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https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
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7 January 2021
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Dose-finding study with nimodipine: a selective central nervous system calcium channel blocker on aminophylline induced seizure models in rats
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7 January 2021
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A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
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7 January 2021
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Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant mice.
1 reference
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7 January 2021
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A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
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https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the Cacnl1a4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic basis of the human epilepsies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Incidence of epilepsy and unprovoked seizures in Rochester, Minnesota: 1935-1984.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
A novel SCN4A mutation causing myotonia aggravated by cold and potassium
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mutation of CHRNA4 responsible for autosomal dominant nocturnal frontal lobe epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mutation ofKCNQ3 (c.925T?C) in a Japanese family with benign familial neonatal convulsions
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Voltage-gated ion channelopathies: inherited disorders caused by abnormal sodium, chloride, and calcium regulation in skeletal muscle
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Electroclinical picture of autosomal dominant nocturnal frontal lobe epilepsy in a Japanese family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A calcium channel mutation causing hypokalemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A family with autosomal dominant nocturnal frontal lobe epilepsy and mental retardation.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
The skeletal muscle chloride channel in dominant and recessive human myotonia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Psychotogenicity and N-methyl-D-aspartate receptor antagonism: implications for neuroprotective pharmacotherapy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation causing autosomal dominant nocturnal frontal lobe epilepsy alters Ca2+ permeability, conductance, and gating of human alpha4beta2 nicotinic acetylcholine receptors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Unstable insertion in the 5' flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Benign familial neonatal convulsions linked to genetic markers on chromosome 20.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human sodium channel myotonia: slowed channel inactivation due to substitutions for a glycine within the III-IV linker
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autoantibodies to the Glutamate Receptor Kill Neurons via Activation of the Receptor Ion Channel
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new locus for generalized epilepsy with febrile seizures plus maps to chromosome 2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic organization of the human muscle chloride channel CIC-1 and analysis of novel mutations leading to Becker-type myotonia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel mutations in families with unusual and variable disorders of the skeletal muscle sodium channel
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Temperature-sensitive mutations in the III–IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenita
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Which GABAA-receptor subtypes really occur in the brain?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification and preclinical testing of novel antiepileptic compounds
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular distinction between fetal and adult forms of muscle acetylcholine receptor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effects of carbamazepine on acetylcholine release and metabolism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Developmental and regional expression in the rat brain and functional properties of four NMDA receptors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glutamate-operated channels: developmentally early and mature forms arise by alternative splicing.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a new locus for generalized epilepsy with febrile seizures plus (GEFS+) on chromosome 2q24-q33.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Channelopathies: ion channel disorders of muscle as a paradigm for paroxysmal disorders of the nervous system
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a mutation in the gene causing hyperkalemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dihydropyridine receptor mutations cause hypokalemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A Met-to-Val mutation in the skeletal muscle Na+ channel alpha-subunit in hyperkalaemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nicotinic receptors in the development and modulation of CNS synapses.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The novel anticonvulsant AWD 140-190 acts as a highly use-dependent sodium channel blocker in neuronal cell preparations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
KVLQT1 mutations in three families with familial or sporadic long QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Benign familial neonatal convulsions: Evidence for clinical and genetic heterogeneity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorder
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
KCNE1 mutations cause jervell and Lange-Nielsen syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Normal cerebellar development but susceptibility to seizures in mice lacking G protein-coupled, inwardly rectifying K+ channel GIRK2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletion of the K(V)1.1 potassium channel causes epilepsy in mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the hminK gene cause long QT syndrome and suppress IKs function
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The GABAA receptors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
D-23129: a potent anticonvulsant in the amygdala kindling model of complex partial seizures
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Radicals r'aging
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An amino acid exchange in the second transmembrane segment of a neuronal nicotinic receptor causes partial epilepsy by altering its desensitization kinetics
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Upregulation of L-type Ca2+ channels in reactive astrocytes after brain injury, hypomyelination, and ischemia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparative anticonvulsant and mechanistic profile of the established and newer antiepileptic drugs
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Guidelines for human gene nomenclature (1997). HUGO Nomenclature Committee.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Presynaptic nicotinic ACh receptors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2800%2900141-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0920-1211(00)00141-8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10962210
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10962210%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
PubMed publication ID
10962210
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10962210
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10962210%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 November 2019
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