Severe myoclonic epilepsy of infants (Dravet syndrome): natural history and neuropsychological findings.
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Low-dose fenfluramine in the treatment of neurologic disorders: experience in Dravet syndromeA Novel Long-term, Multi-Channel and Non-invasive Electrophysiology Platform for Zebrafish.Psychosocial aspects of epilepsy: a wider approachOn the multiple roles of the voltage gated sodium channel β1 subunit in genetic diseasesA novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disordersClinical review of genetic epileptic encephalopathiesEpilepsy and Autism.Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females.Curing epilepsy: progress and future directionsLarge-scale structural alteration of brain in epileptic children with SCN1A mutationImpaired excitability of somatostatin- and parvalbumin-expressing cortical interneurons in a mouse model of Dravet syndromeStiripentol : in severe myoclonic epilepsy of infancy (dravet syndrome).Encephalopathy in children with Dravet syndrome is not a pure consequence of epilepsyDravet 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.Na(V)1.1 channels are critical for intercellular communication in the suprachiasmatic nucleus and for normal circadian rhythmsPharmacotherapy for Dravet Syndrome.Cognitive Deficits Associated with Nav1.1 Alterations: Involvement of Neuronal Firing Dynamics and OscillationsAutistic-like behaviour in Scn1a+/- mice and rescue by enhanced GABA-mediated neurotransmission.Epileptic encephalopathies in adults and childhood.When should clinicians order genetic testing for Dravet syndrome?Focal Scn1a knockdown induces cognitive impairment without seizures.Upregulation of Haploinsufficient Gene Expression in the Brain by Targeting a Long Non-coding RNA Improves Seizure Phenotype in a Model of Dravet Syndrome.Temperature-dependent changes in neuronal dynamics in a patient with an SCN1A mutation and hyperthermia induced seizuresHuperzine A Provides Robust and Sustained Protection against Induced Seizures in Scn1a Mutant Mice.A functional null mutation of SCN1B in a patient with Dravet syndrome.Comorbidities in pediatric epilepsy: beyond "just'' treating the seizures.SCN1A Gene Mutation and Adaptive Functioning in 18 Vietnamese Children with Dravet Syndrome.Patient considerations in the management of focal seizures in children and adolescents.Cognitive and behavioral characteristics of children with Dravet syndrome: an overview.Cognitive development in children with Dravet syndrome.Dravet syndrome and SCN1A gene mutation related-epilepsies: cognitive impairment and its determinants.Current therapeutic procedures in Dravet syndrome."Epileptic encephalopathy" of infancy and childhood: electro-clinical pictures and recent understandingsNa+ channelopathies and epilepsy: recent advances and new perspectives."Electro-clinical syndromes" with onset in paediatric age: the highlights of the clinical-EEG, genetic and therapeutic advances.SCN1A mutations in Dravet syndrome: impact of interneuron dysfunction on neural networks and cognitive outcome.Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders.Dravet syndrome--from epileptic encephalopathy to channelopathy.Untangling the dravet syndrome seizure network: the changing face of a rare genetic epilepsy
P2860
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P2860
Severe myoclonic epilepsy of infants (Dravet syndrome): natural history and neuropsychological findings.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh-hant
name
Severe myoclonic epilepsy of i ...... d neuropsychological findings.
@en
Severe myoclonic epilepsy of infants
@nl
type
label
Severe myoclonic epilepsy of i ...... d neuropsychological findings.
@en
Severe myoclonic epilepsy of infants
@nl
prefLabel
Severe myoclonic epilepsy of i ...... d neuropsychological findings.
@en
Severe myoclonic epilepsy of infants
@nl
P2093
P1433
P1476
Severe myoclonic epilepsy of i ...... d neuropsychological findings.
@en
P2093
Catherine Cassé-Perrot
Charlotte Dravet
Markus Wolff
P2860
P356
10.1111/J.1528-1167.2006.00688.X
P478
47 Suppl 2
P577
2006-01-01T00:00:00Z