Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?
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Characterization of a de novo SCN8A mutation in a patient with epileptic encephalopathyChannelopathiesCognitive impairment in childhood onset epilepsy: up-to-date information about its causesGenetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndromeAxon initial segment dysfunction in a mouse model of genetic epilepsy with febrile seizures plus.Mapping genetic modifiers of survival in a mouse model of Dravet syndrome.Knock-in model of Dravet syndrome reveals a constitutive and conditional reduction in sodium current.A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndromeGenetic testing in the epilepsies--report of the ILAE Genetics CommissionLarge-scale structural alteration of brain in epileptic children with SCN1A mutationLack of replication of association between scn1a SNP and febrile seizures.Role of the axonal initial segment in psychiatric disorders: function, dysfunction, and interventionA new locus on chromosome 22q13.31 linked to recessive genetic epilepsy with febrile seizures plus (GEFS+) in a Tunisian consanguineous familyDravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology.Rare copy number variants are an important cause of epileptic encephalopathies.Genetics of temporal lobe epilepsy: a review.Vagus nerve stimulation for genetic epilepsy with febrile seizures plus (GEFS+) accompanying seizures with impaired consciousnessEpileptic encephalopathies in adults and childhood.Novel GABRG2 mutations cause familial febrile seizuresGenetic forms of epilepsies and other paroxysmal disordersChipping away at the common epilepsies with complex genetics: the 15q13.3 microdeletion shows the way.Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+.Severe epilepsy syndromes of early childhood: the link between genetics and pathophysiology with a focus on SCN1A mutations.NaV1.1 channels and epilepsy.Axon initial segment dysfunction in epilepsy.Sodium channel SCN1A and epilepsy: mutations and mechanisms.Blinders, phenotype, and fashionable genetic analysis: a critical examination of the current state of epilepsy genetic studies.The sleep manifestations of frontal lobe epilepsy."Epileptic encephalopathy" of infancy and childhood: electro-clinical pictures and recent understandingsPharmacogenomics and epilepsy: the road ahead.SCN1A mutations in Dravet syndrome: impact of interneuron dysfunction on neural networks and cognitive outcome.Sodium channels and the neurobiology of epilepsy.Fever and fever-related epilepsies.The genetics of the epilepsies.Diagnostic Approach to Genetic Causes of Early-Onset Epileptic Encephalopathy.Helping Families Cope with the Severe Stress of Dravet Syndrome.Modeling Dravet syndrome using induced pluripotent stem cells (iPSCs) and directly converted neurons.The role of genetic testing in epilepsy diagnosis and management.Familial aggregation of focal seizure semiology in the Epilepsy Phenome/Genome Project.SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures
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Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?
description
article científic
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article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 08 February 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?
@en
Dravet syndrome or genetic
@nl
type
label
Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?
@en
Dravet syndrome or genetic
@nl
prefLabel
Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?
@en
Dravet syndrome or genetic
@nl
P1476
Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?
@en
P2093
Floor E Jansen
Ingrid E Scheffer
P304
P356
10.1016/J.BRAINDEV.2009.01.001
P577
2009-02-08T00:00:00Z