about
Screening of conventional anticonvulsants in a genetic mouse model of epilepsy.Initial Treatment for Nonsyndromic Early-Life Epilepsy: An Unexpected Consensus.Cardiovascular safety of low-dose fenfluramine in Dravet syndrome: a review of its benefit-risk profile in a new patient population.The Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Epilepsy in Paediatric Patients.Models for discovery of targeted therapy in genetic epileptic encephalopathies.The synthetic neuroactive steroid SGE-516 reduces seizure burden and improves survival in a Dravet syndrome mouse model.Quality of life and comorbidities associated with Dravet syndrome severity: a multinational cohort survey.Progress in Understanding and Treating SCN2A-Mediated Disorders.Preclinical Animal Models for Dravet Syndrome: Seizure Phenotypes, Comorbidities and Drug Screening.Mutations in SCN3A cause early infantile epileptic encephalopathy
P2860
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P2860
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Treatment of Dravet Syndrome.
@en
type
label
Treatment of Dravet Syndrome.
@en
prefLabel
Treatment of Dravet Syndrome.
@en
P2860
P356
P1476
Treatment of Dravet Syndrome.
@en
P2093
Elaine C Wirrell
P2860
P356
10.1017/CJN.2016.249
P478
43 Suppl 3
P577
2016-06-01T00:00:00Z