Katrien Smets

ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology

The state of artificial intelligence-based FDA-approved medical devices and algorithms: an online database

Benchmarking the stability of human detergent-solubilised voltage-gated sodium channels for structural studies using eel as a reference

Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome

Therapeutic potential of NaV1.1 activators

Multimodal wrist-worn devices for seizure detection and advancing research: Focus on the Empatica wristbands

Na_V1.1 channels and epilepsy

Selective spider toxins reveal a role for the Nav1.1 channel in mechanical pain

Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005–2009

Converging cellular themes for the hereditary spastic paraplegias

PHF8, a gene associated with cleft lip/palate and mental retardation, encodes for an Nε-dimethyl lysine demethylase

Parental mosaicism can cause recurrent transmission ofSCN1A mutations associated with severe myoclonic epilepsy of infancy

novoSNP, a novel computational tool for sequence variation discovery

Autosomal dominant nocturnal frontal lobe epilepsy

Dynamics and functions of lipid droplets

Na_V1.7 Gain-of-Function Mutations as a Continuum: A1632E Displays Physiological Changes Associated with Erythromelalgia and Paroxysmal Extreme Pain Disorder Mutations and Produces Symptoms of Both Disorders

Cellular and Molecular Mechanisms of Pain

Genome-Wide Copy Number Variation in Epilepsy: Novel Susceptibility Loci in Idiopathic Generalized and Focal Epilepsies

Sodium channelSCN1Aand epilepsy: Mutations and mechanisms

Mapping short DNA sequencing reads and calling variants using mapping quality scores

The hitchhiker’s guide to the voltage-gated sodium channel galaxy

Impaired excitability of somatostatin- and parvalbumin-expressing cortical interneurons in a mouse model of Dravet syndrome

Pharmacology of the Na _v 1.1 domain IV voltage sensor reveals coupling between inactivation gating processes

Na_v1.1 Modulation by a Novel Triazole Compound Attenuates Epileptic Seizures in Rodents

Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development

Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48)

De novoSCN1Amutations are a major cause of severe myoclonic epilepsy of infancy

TheSCN1Avariant database: a novel research and diagnostic tool

Automated non-EEG based seizure detection: Do users have a say?