about
Genetic epilepsy syndromes without structural brain abnormalities: clinical features and experimental modelsRole of voltage-gated calcium channels in epilepsy.Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus.A balanced chromosomal translocation disrupting ARHGEF9 is associated with epilepsy, anxiety, aggression, and mental retardation.Nocturnal frontal lobe epilepsy with paroxysmal arousals due to CHRNA2 loss of functionFamilial hemiplegic migraine.Osteopenia due to enhanced cathepsin K release by BK channel ablation in osteoclasts.Genetics of epilepsy: The testimony of twins in the molecular eraGenetically complex epilepsies, copy number variants and syndrome constellations.A novel GABRG2 mutation, p.R136*, in a family with GEFS+ and extended phenotypes.Ion channel pharmacology.Functional properties and differential neuromodulation of Na(v)1.6 channels.Candidate genes for idiopathic epilepsy in four dog breeds.Idiopathic generalized epilepsy and hypokalemic periodic paralysis in a family of South Indian descent.Finding Channels.No relation between EFHC2 gene polymorphism and Idiopathic generalized epilepsyModel systems for studying cellular mechanisms of SCN1A-related epilepsy.Challenges in the design and conduct of therapeutic trials in channel disorders.A polygenic heterogeneity model for common epilepsies with complex genetics.Epilepsy, E/I Balance and GABA(A) Receptor Plasticity.A review of potassium channels in bipolar disorder.Genetic variations and associated pathophysiology in the management of epilepsy.Chipping away at the common epilepsies with complex genetics: the 15q13.3 microdeletion shows the way.Forty years from markers to genes.Genetically encoded optical sensors for monitoring of intracellular chloride and chloride-selective channel activity.Development of individualized medicine for epilepsy based on genetic information.Targeting voltage-gated calcium channels in neurological and psychiatric diseases.Functional modulation of voltage-dependent sodium channel expression by wild type and mutated C121W-β1 subunit.Prevalence of Epilepsy among Cataract Patients.Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures.KCNT1 mutations in ADNFLE and MMPSI: a new driver in the etiology and pathophysiology of early-onset epileptic syndromes.A Subset of Dogs with Presumptive Idiopathic Epilepsy Show Hippocampal Asymmetry: A Volumetric Comparison with Non-Epileptic Dogs Using MRI.Nocturnal frontal lobe epilepsy.First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy.A Longitudinal Study of Survival in Belgian Shepherds with Genetic EpilepsySleep Related Epilepsy and Pharmacotherapy: An InsightMissense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy
P2860
Q26861471-36B67FD7-2437-4889-832F-6CEB1B93266FQ30427731-DD1FFCCD-B43E-4A92-8ED7-496024178C68Q30498134-80CC72F7-51D4-4478-B31F-05AA8BA7D471Q30538580-563D0AD7-45F8-4751-A334-D5A86AAE76EEQ30642893-0E63FC75-8929-4EA8-B7C6-17D0A1BE5665Q33280531-80A936A5-AAB9-4D04-91B0-BFDD383FA5A0Q33939383-37547D8E-70C5-4F26-8B49-3CC4ACFF9842Q34198753-E0DA30A6-70F1-4798-A9C0-E861F3CFA52BQ34334100-6F0B39D3-0C76-4142-83DB-1280926308F3Q34464870-969F474C-5008-40A7-9054-B5A78B4ABD3DQ34613758-4481AD88-AAE1-4029-9AB8-98F466DABC73Q34791973-CC34951D-678C-4434-A1D5-61F9084D7C8BQ35035419-0F553540-F16D-4EE9-ACFB-E912E9EE0DB1Q35373045-278E845A-6DE4-4508-9B45-BEB72EF555FBQ36301315-D8D49DF1-FD0F-44BF-9AC1-2610EE344CBEQ36612676-C0D2745C-3FB6-4955-9439-8F06AA5860ECQ36760270-246B6F11-E1ED-44FD-8A82-A786020E0F64Q36774698-88126B3E-8AC4-4F57-8E18-65DBA3A7E827Q36845174-6173DC39-0586-4E20-B11F-5A135E21B1B3Q36852883-C62A048D-6D46-4865-9732-8811196B2CA4Q36917377-8E55100D-E444-4749-818C-8B33EC7824AAQ36925220-7BE3F4DC-EE79-4A16-BA8C-4904C37C9E6FQ37149241-0CA180BE-FCFE-472F-B172-AE025BBACAAFQ37220081-8466C529-559B-450A-9177-8BCEAFD4FA39Q37670661-117DA58C-B8E7-4808-979E-B49354F30D9BQ38178326-FDA532D9-3BB0-43AF-A084-0F2B80C6FC62Q38626606-B36BCA90-D332-4B65-BDDA-AB3AC75F8F7AQ39166783-61DCD1E0-E05E-4D7A-BF86-EC73445D1460Q43064770-79595E01-867D-49C5-97A4-6FB0EBF7D260Q43166554-630ECF5A-1311-4A42-8058-7C2844873912Q45022179-7F44E34D-61E5-4AEF-A277-E6D16D11E7BAQ47109647-61A01275-0A15-494F-9023-47D852012530Q48133335-480A3A30-3DBF-40D5-9A75-FF0C7734A3BFQ51819010-C7E64064-B43E-41B6-B25B-7E07A06953CCQ56639393-8D112164-A5FC-4217-A0AB-DBFF5A24EF97Q57490979-157F4B4D-0ED6-4496-B5A5-A31847B52127Q57767434-A3DF26A2-B25D-4002-B825-6C94F590C7B5
P2860
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
Channelopathies in idiopathic epilepsy.
@ast
Channelopathies in idiopathic epilepsy.
@en
type
label
Channelopathies in idiopathic epilepsy.
@ast
Channelopathies in idiopathic epilepsy.
@en
prefLabel
Channelopathies in idiopathic epilepsy.
@ast
Channelopathies in idiopathic epilepsy.
@en
P2860
P50
P1433
P1476
Channelopathies in idiopathic epilepsy.
@en
P2093
John C Mulley
Leanne M Dibbens
P2860
P2888
P304
P356
10.1016/J.NURT.2007.01.009
P577
2007-04-01T00:00:00Z
P5875
P6179
1017769091