A long-term follow-up study of Dravet syndrome up to adulthood.
about
Sudden unexpected death in a mouse model of Dravet syndrome.Neuroimaging and neuropathology of Dravet syndrome.Tau reduction prevents disease in a mouse model of Dravet syndromeDravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology.Severe Myoclonic Epilepsy in Infancy - Adult Phenotype with Bradykinesia, Hypomimia, and Perseverative Behavior: Report of Five Cases.Maturation of EEG oscillations in children with sodium channel mutations.Pharmacotherapy for Dravet Syndrome.Adult Phenotypes in Angelman- and Rett-Like Syndromes.Focal Scn1a knockdown induces cognitive impairment without seizures.Electroencephalogram of age-dependent epileptic encephalopathies in infancy and early childhood.Huperzine A Provides Robust and Sustained Protection against Induced Seizures in Scn1a Mutant Mice.Audit of use of stiripentol in adults with Dravet syndromeSCN1A Gene Mutation and Adaptive Functioning in 18 Vietnamese Children with Dravet Syndrome.GABRA1 and STXBP1: novel genetic causes of Dravet syndrome.Electroencephalographic characteristics of Dravet syndrome.Cognitive and behavioral characteristics of children with Dravet syndrome: an overview.Cognitive development in children with Dravet syndrome.Dravet syndrome: the long-term outcome.SCN1A mutations in Dravet syndrome: impact of interneuron dysfunction on neural networks and cognitive outcome.Dravet syndrome: seizure control and gait in adults with different SCN1A mutations.The ketogenic diet in Dravet syndrome.Stiripentol in Dravet syndrome: results of a retrospective U.S. study.The SCN1A gene variants and epileptic encephalopathies.Cardiovascular safety of low-dose fenfluramine in Dravet syndrome: a review of its benefit-risk profile in a new patient population.Stiripentol and vigabatrin current roles in the treatment of epilepsy.Co-occurring malformations of cortical development and SCN1A gene mutations.Dravet syndrome--considerable delay in making the diagnosis.Dravet syndrome: new potential genetic modifiers, imaging abnormalities, and ictal findings.Variability of EEG-fMRI findings in patients with SCN1A-positive Dravet syndrome.Electroencephalographic features in dravet syndrome: five-year follow-up study in 22 patients.Transition to adult life in the monogenic epilepsies.Successful use of fenfluramine as an add-on treatment for Dravet syndrome.Five-year extended follow-up status of 10 patients with Dravet syndrome treated with fenfluramine.A prospective open-label trial of a CBD/THC cannabis oil in dravet syndrome
P2860
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P2860
A long-term follow-up study of Dravet syndrome up to adulthood.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh-hant
name
A long-term follow-up study of Dravet syndrome up to adulthood.
@en
A long-term follow-up study of Dravet syndrome up to adulthood.
@nl
type
label
A long-term follow-up study of Dravet syndrome up to adulthood.
@en
A long-term follow-up study of Dravet syndrome up to adulthood.
@nl
prefLabel
A long-term follow-up study of Dravet syndrome up to adulthood.
@en
A long-term follow-up study of Dravet syndrome up to adulthood.
@nl
P2093
P1433
P1476
A long-term follow-up study of Dravet syndrome up to adulthood.
@en
P2093
Harumi Yoshinaga
Katsuhiro Kobayashi
Mari Akiyama
Yoko Ohtsuka
P304
P356
10.1111/J.1528-1167.2009.02466.X
P577
2009-12-22T00:00:00Z