Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.
about
Calcium antagonists as an add-on therapy for drug-resistant epilepsyThe Revolution in Migraine Genetics: From Aching Channels Disorders to a Next-Generation MedicineThe Physiology, Pathology, and Pharmacology of Voltage-Gated Calcium Channels and Their Future Therapeutic PotentialGenetic disruption of voltage-gated calcium channels in psychiatric and neurological disordersMolecular pathophysiology and pharmacology of the voltage-sensing module of neuronal ion channelsThe neurobiology of antiepileptic drugsMutations in EFHC1 cause juvenile myoclonic epilepsyFamilial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2+ channel gating: evidence for beta-subunit isoform-specific effectsThe role of positive selection in determining the molecular cause of species differences in diseaseRole of voltage-gated calcium channels in epilepsy.Dominant-negative suppression of Cav2.1 currents by alpha(1)2.1 truncations requires the conserved interaction domain for beta subunits.Genotype-phenotype relationship in three cases with overlapping 19p13.12 microdeletions.Calcium channel dysfunction in inferior colliculus neurons of the genetically epilepsy-prone ratGenetic and hormonal factors modulate spreading depression and transient hemiparesis in mouse models of familial hemiplegic migraine type 1.CaV 2.1 ablation in cortical interneurons selectively impairs fast-spiking basket cells and causes generalized seizures.Childhood absence epilepsy: genes, channels, neurons and networks.Dominant-negative effect of SCN5A N-terminal mutations through the interaction of Na(v)1.5 α-subunitsCellular and network mechanisms of spike-wave seizures.The genetic relationship between epilepsy and hemiplegic migraineGenetic testing in the epilepsies--report of the ILAE Genetics CommissionUnraveling monogenic channelopathies and their implications for complex polygenic diseaseParoxysmal dyskinesias in miceDoes epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?GABAA Receptor Expression in the Forebrain of Ataxic Rolling Nagoya MiceA genetic interaction network model of a complex neurological disease.Transcriptome analysis of neonatal larvae after hyperthermia-induced seizures in the contractile silkworm, Bombyx mori.The neuronal channelopathies.Genetics of migraine: possible links to neurophysiological abnormalities.Migraine genetics.Polymorphisms of the SCN1A gene in children and adolescents with primary headache and idiopathic or cryptogenic epilepsy: is there a linkage?Genetics and function of neocortical GABAergic interneurons in neurodevelopmental disordersLarge Genomic Deletions in CACNA1A Cause Episodic Ataxia Type 2Abnormal excitability and episodic low-frequency oscillations in the cerebral cortex of the tottering mouse.Idiopathic generalized epilepsy and hypokalemic periodic paralysis in a family of South Indian descent.Persistent abnormality detected in the non-ictal electroencephalogram in primary generalised epilepsy.Genomic aberrations of the CACNA2D1 gene in three patients with epilepsy and intellectual disabilityGenetics of photosensitivity (photoparoxysmal response): a review.Advances in imaging ultrastructure yield new insights into presynaptic biologyDysgraphia as a Mild Expression of Dystonia in Children with Absence EpilepsyMolecular basis of Mendelian idiopathic epilepsies.
P2860
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P2860
Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.
description
2001 nî lūn-bûn
@nan
2001 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.
@ast
Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.
@en
Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.
@nl
type
label
Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.
@ast
Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.
@en
Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.
@nl
prefLabel
Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.
@ast
Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.
@en
Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.
@nl
P2093
P1433
P1476
Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.
@en
P2093
A Jouvenceau
A Spauschus
D M Kullmann
L H Eunson
S M Zuberi
P304
P356
10.1016/S0140-6736(01)05971-2
P407
P577
2001-09-01T00:00:00Z