Epileptogenic channelopathies: experimental models of human pathologies.
about
Phenytoin inhibits the persistent sodium current in neocortical neurons by modifying its inactivation propertiesTemporal and topographic alterations in expression of the alpha3 isoform of Na+, K(+)-ATPase in the rat freeze lesion model of microgyria and epileptogenesisGenetics and epilepsy.Decreased hyperpolarization-activated currents in layer 5 pyramidal neurons enhances excitability in focal cortical dysplasia.Epilepsy as a neurodevelopmental disorder.Genomic organization, expression, and phylogenetic analysis of Ca2+ channel beta4 genes in 13 vertebrate species.A functional null mutation of SCN1B in a patient with Dravet syndrome.Early life stress as an influence on limbic epilepsy: an hypothesis whose time has come?Double Trouble? Potential for Hyperexcitability Following Both Channelopathic up- and Downregulation of I(h) in Epilepsy.Blood DNA methylation pattern is altered in mesial temporal lobe epilepsyThe genetics of Dravet syndrome.Dravet syndrome: insights from in vitro experimental models.Na+ channelopathies and epilepsy: recent advances and new perspectives.Dysfunctional HCN ion channels in neurological diseases.Genetic loss of HCN1 channels is exciting, but is it epileptic?Self-limited hyperexcitability: functional effect of a familial hemiplegic migraine mutation of the Nav1.1 (SCN1A) Na+ channel.A century of achievements.Remapping and mutation analysis of benign adult familial myoclonic epilepsy in a Japanese pedigree.
P2860
Q28485346-812BFD4B-AD82-4671-9AD2-6C3B5006738BQ28572675-FB491077-17E4-49B6-966D-9F85F2A96623Q30473411-2C86EE53-83C5-4797-9FA0-5FE785EF914DQ35543912-B261D5B4-85E5-4195-9E9D-749EFC0549D2Q35838099-E493BFD4-0CDF-420A-A180-B6B6521F9006Q36956228-B9164F74-FC8F-4293-9A12-AE93635B7858Q37359854-1EA2CA3E-E3A5-41A0-B0F6-5C700F3AB1ADQ37388479-D7909459-6E6C-4787-997D-BDD58CF7A935Q37596976-C8916102-F38C-4B1E-BBF1-CE560959BC4AQ37690173-8669A937-B640-4E43-947A-3C7789520990Q37861258-B1413628-A184-42D2-BC74-61085E60E2FAQ37861268-0FF1CB75-ED43-4D5D-8369-C1A14CEDF707Q37960093-028BAF5B-BB4B-4690-858E-42797917A397Q38389906-057A90C0-1894-4233-914C-8C9C7B90654DQ39553828-EF9BF746-2F8E-4B9C-97B1-3C6AC971C237Q39960558-5BB769A3-38D0-4BC9-A399-F2885C48711AQ47298956-DCDAB381-632E-443B-9A2E-326E65B13126Q50262946-712BBD17-739F-4C11-8CBC-355ECCE7FC42
P2860
Epileptogenic channelopathies: experimental models of human pathologies.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Epileptogenic channelopathies: experimental models of human pathologies.
@en
type
label
Epileptogenic channelopathies: experimental models of human pathologies.
@en
prefLabel
Epileptogenic channelopathies: experimental models of human pathologies.
@en
P2860
P1433
P1476
Epileptogenic channelopathies: experimental models of human pathologies
@en
P2093
Giuliano Avanzini
Silvana Franceschetti
P2860
P356
10.1111/J.1528-1167.2007.01067.X
P478
48 Suppl 2
P577
2007-01-01T00:00:00Z