(Q33534658)

27 July 2017

1 reference

title

Ion channels and the genetic contribution to epilepsy (English)

1 reference

27 July 2017

S G Ryan

1

1 reference

PubMed ID

10025538

27 July 2017

language of work or name

1 reference

1 January 1999

1 reference

Journal of Child Neurology

27 July 2017

1 reference

27 July 2017

14

1 reference

27 July 2017

58-66

1 reference

27 July 2017

1

1 reference

Incidence of epilepsy and unprovoked seizures in Rochester, Minnesota: 1935-1984.

27 July 2017

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Genetic epidemiology of epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

21 January 2018

Post-traumatic epilepsy.

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

The future of genetic studies of complex human diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Benign familial neonatal convulsions: Evidence for clinical and genetic heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Benign familial neonatal convulsions: generalized epilepsy?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Neonate with benign familial neonatal convulsions: recorded generalized and focal seizures.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Benign familial neonatal convulsions linked to genetic markers on chromosome 20.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Searching for human epilepsy genes: a progress report.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

A potassium channel mutation in neonatal human epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Eight potassium channel families revealed by the C. elegans genome project.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Genetics, molecular mechanisms and management of long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Impulse activity and the patterning of connections during CNS development

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Autosomal dominant nocturnal frontal lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Autosomal dominant nocturnal frontal lobe epilepsy. A video-polysomnographic and genetic appraisal of 40 patients and delineation of the epileptic syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Differential diagnosis of sleep disorders, non-epileptic attacks and epileptic seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Absence epilepsy in tottering mutant mice is associated with calcium channel defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Distinctive pharmacology and kinetics of cloned neuronal Ca2+ channels and their possible counterparts in mammalian CNS neurons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Molecular biology of calcium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Sensory gating mechanisms of the thalamus

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Low-threshold calcium currents in central nervous system neurons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Characterization of ethosuximide reduction of low-threshold calcium current in thalamic neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Molecular characterization of a neuronal low-voltage-activated T-type calcium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Mutant mouse tottering: selective increase of locus ceruleus axons in a defined single-locus mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

A single gene error of noradrenergic axon growth synchronizes central neurones

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

The role of GABAB receptor activation in absence seizures of lethargic (lh/lh) mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Increased excitability and inward rectification in layer V cortical pyramidal neurons in the epileptic mutant mouse Stargazer

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Periodicity of thalamic synchronized oscillations: the role of Ca2+-mediated upregulation of Ih.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Hormonal regulation, pharmacology, and membrane sorting of vertebrate Na+/H+ exchanger isoforms

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

21 January 2018

Targeting epilepsy genes

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Altered synaptic physiology and reduced susceptibility to kainate-induced seizures in GluR6-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Normal cerebellar development but susceptibility to seizures in mice lacking G protein-coupled, inwardly rectifying K+ channel GIRK2

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Deletion of the K(V)1.1 potassium channel causes epilepsy in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

Angelman syndrome: correlations between epilepsy phenotypes and genotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400104

10.1177/088307389901400104

21 January 2018

Identifiers

DOI

0 references

PubMed ID

10025538

1 reference

PubMed ID

10025538