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Pharmacological characterization of an antisense knockdown zebrafish model of Dravet syndrome: inhibition of epileptic seizures by the serotonin agonist fenfluramineThe genetics of auricular development and malformation: new findings in model systems driving future directions for microtia research.Seizure Reduction with Fluoxetine in Dravet Syndrome.Analysis of endocannabinoid signaling elements and related proteins in lymphocytes of patients with Dravet syndromeBest practice guidelines for the use of next-generation sequencing applications in genome diagnostics: a national collaborative study of Dutch genome diagnostic laboratories.Actual insights into the clinical management of febrile seizures.Pharmacological considerations in the use of stiripentol for the treatment of epilepsy.The Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Epilepsy in Paediatric Patients.Co-occurring malformations of cortical development and SCN1A gene mutations.Paradoxical proepileptic response to NMDA receptor blockade linked to cortical interneuron defect in stargazer miceSomatosensory reflex seizures in a child with epilepsy related to novel SCN1A mutation.Tetrodotoxin, a Candidate Drug for Nav1.1-Induced Mechanical Pain?
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Dravet syndrome: the main issues.
@en
type
label
Dravet syndrome: the main issues.
@en
prefLabel
Dravet syndrome: the main issues.
@en
P1476
Dravet syndrome: the main issues.
@en
P2093
Renzo Guerrini
P356
10.1016/J.EJPN.2012.04.006
P478
16 Suppl 1
P577
2012-06-15T00:00:00Z