Are some idiopathic epilepsies disorders of ion channels?: A working hypothesis. (Q34016353)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10962210%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

review article

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title

Are some idiopathic epilepsies disorders of ion channels?: A working hypothesis (English)

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9 November 2019

1

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9 November 2019

Motohiro Okada

series ordinal

2

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9 November 2019

author name string

S Kaneko

series ordinal

3

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9 November 2019

A Mitsudome

series ordinal

4

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9 November 2019

publication date

1 October 2000

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9 November 2019

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9 November 2019

volume

41

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9 November 2019

issue

3

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9 November 2019

page(s)

191-204

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MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

9 November 2019

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Missense mutation in the pore region of HERG causes familial long QT syndrome

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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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A potassium channel mutation in neonatal human epilepsy

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High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2

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Mutations in the Cacnl1a4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice

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Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia

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A novel SCN4A mutation causing myotonia aggravated by cold and potassium

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A novel mutation of CHRNA4 responsible for autosomal dominant nocturnal frontal lobe epilepsy

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A novel mutation ofKCNQ3 (c.925T?C) in a Japanese family with benign familial neonatal convulsions

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7 January 2021

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Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)

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7 January 2021

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Unstable insertion in the 5' flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1

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7 January 2021

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7 January 2021

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KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel

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Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

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Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.

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An amino acid exchange in the second transmembrane segment of a neuronal nicotinic receptor causes partial epilepsy by altering its desensitization kinetics

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Presynaptic nicotinic ACh receptors

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A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy

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Identifiers

DOI

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9 November 2019

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