Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome.
about
Febrile Seizures and Febrile Seizure Syndromes: An Updated Overview of Old and Current KnowledgeCommunity structure analysis of transcriptional networks reveals distinct molecular pathways for early- and late-onset temporal lobe epilepsy with childhood febrile seizuresA variant of KCC2 from patients with febrile seizures impairs neuronal Cl- extrusion and dendritic spine formationNext-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairmentAssociation of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism.Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform.Short-lasting unilateral neuralgiform headache attacks with ispilateral facial flushing is a new variant of paroxysmal extreme pain disorder.Atypical benign partial epilepsy of childhood with acquired neurocognitive, lexical semantic, and autistic spectrum disorder.Genetic Variants Identified from Epilepsy of Unknown Etiology in Chinese Children by Targeted Exome Sequencing.Dravet Syndrome: Diagnosis and Long-Term Course.Dravet syndrome and its mimics: Beyond SCN1A.Not all SCN1A epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotypeEarly onset epileptic encephalopathy caused by de novo SCN8A mutations.Comparison and optimization of in silico algorithms for predicting the pathogenicity of sodium channel variants in epilepsy.The Na1.7 Channel Subtype as an Antinociceptive Target for Spider Toxins in Adult Dorsal Root Ganglia Neurons
P2860
Q26772260-60748ED5-4E12-47C5-A5C9-EEB7C7F2ED2FQ27305647-2AC95067-B397-4B86-9960-7B71D54A2DFEQ28116504-572A6587-61BB-4853-99F0-838AF095CA5DQ33601252-26F71F2A-C7BA-468D-86A5-48FFEF4A4C71Q33790438-DD850CFB-6852-4758-BF25-D69BD663E691Q35079979-F40B57E5-A3D4-40E1-A870-CD5FFABFF683Q35554540-2A534B89-9B8F-415B-99EE-428E4347194CQ37143592-4AD45533-4D06-4434-9670-C98BE54BB2B0Q37579472-30CC9DB4-66B9-462D-BEB5-D61E10A374E5Q38855478-BC0804E1-6D6B-48D0-9CF3-9D1820C2CFA6Q40040294-7D206A6E-46BA-4482-B2E3-1B4BDCBB6834Q41543515-B9AC24B1-B53C-49C5-A3FF-086811A1CF46Q45736221-A43FE86B-439E-4D7D-A688-A437FE398BB9Q47840577-FCF91B49-183C-42D3-A975-4B374CC10177Q58764681-EEF0C003-7B1C-44AE-AC63-952A594F8FA8
P2860
Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh-hant
name
Role of the sodium channel SCN ...... ures plus and Dravet syndrome.
@en
Role of the sodium channel SCN ...... ures plus and Dravet syndrome.
@nl
type
label
Role of the sodium channel SCN ...... ures plus and Dravet syndrome.
@en
Role of the sodium channel SCN ...... ures plus and Dravet syndrome.
@nl
prefLabel
Role of the sodium channel SCN ...... ures plus and Dravet syndrome.
@en
Role of the sodium channel SCN ...... ures plus and Dravet syndrome.
@nl
P2093
P2860
P50
P356
P1433
P1476
Role of the sodium channel SCN ...... ures plus and Dravet syndrome.
@en
P2093
Andrew Bleasel
Bree Hodgson
Elaine C Wirrell
Eva Andermann
John C Mulley
Kevin Farrell
Leanne M Dibbens
Lynette Sadleir
Mark Mackay
Michael Harbord
P2860
P304
P356
10.1111/EPI.12323
P577
2013-07-29T00:00:00Z