Quantitative analysis and EEG markers of KCNT1 epilepsy of infancy with migrating focal seizures

Clinical and molecular characterization ofKCNT1-related severe early-onset epilepsy

(2017) Amy McTague et al.   NEUROLOGY

Ineffective quinidine therapy in early onset epileptic encephalopathy withKCNT1mutation

(2016) Pin Fee Chong et al.   ANNALS OF NEUROLOGY

Dynamic changes of depolarizing GABA in a computational model of epileptogenic brain: Insight for Dravet syndrome

(2016) P. Kurbatova et al.   EXPERIMENTAL NEUROLOGY

KCNT1mutations in seizure disorders: the phenotypic spectrum and functional effects

(2016) Chiao Xin Lim et al.   JOURNAL OF MEDICAL GENETICS

Computational models of epileptiform activity

(2016) Fabrice Wendling et al.   JOURNAL OF NEUROSCIENCE METHODS

Characterization of two de novo KCNT1 mutations in children with malignant migrating partial seizures in infancy

(2016) Francesca Rizzo et al.   MOLECULAR AND CELLULAR NEUROSCIENCE

Quinidine in the treatment of KCNT1-positive epilepsies

(2015) Mohamad A Mikati et al.   ANNALS OF NEUROLOGY

The Classical Pathways of Occipital Lobe Epileptic Propagation Revised in the Light of White Matter Dissection

(2015) Francesco Latini et al.   BEHAVIOURAL NEUROLOGY

Characteristic Features of the Interictal EEG Background in 2 Patients With Malignant Migrating Partial Epilepsy in Infancy

(2015) Olga Selioutski et al.   JOURNAL OF CLINICAL NEUROPHYSIOLOGY

Differential distribution of the sodium-activated potassium channels slick and slack in mouse brain

(2015) Sandra Rizzi et al.   JOURNAL OF COMPARATIVE NEUROLOGY

Targeted treatment of migrating partial seizures of infancy with quinidine

(2014) David Bearden et al.   ANNALS OF NEUROLOGY

KCNT1gain of function in 2 epilepsy phenotypes is reversed by quinidine

(2014) Carol J. Milligan et al.   ANNALS OF NEUROLOGY

The Neonatal Connectome During Preterm Brain Development

(2014) Martijn P. van den Heuvel et al.   CEREBRAL CORTEX

Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis

(2014) H. C. Martin et al.   HUMAN MOLECULAR GENETICS

Recommandations françaises sur l’électroencéphalogramme

(2014) N. André-Obadia et al.   NEUROPHYSIOLOGIE CLINIQUE-CLINICAL NEUROPHYSIOLOGY

Human Slack Potassium Channel Mutations Increase Positive Cooperativity between Individual Channels

(2014) Grace E. Kim et al.   Cell Reports

Migrating partial seizures of infancy: expansion of the electroclinical, radiological and pathological disease spectrum

(2013) Amy McTague et al.   BRAIN

Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy

(2012) Sarah E Heron et al.   NATURE GENETICS

De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy

(2012) Giulia Barcia et al.   NATURE GENETICS

Focal seizure propagation in the intracranial EEG

(2010) Sigmund Jenssen et al.   EPILEPSY RESEARCH

Cortical and subcortical networks in human secondarily generalized tonic–clonic seizures

(2009) H. Blumenfeld et al.   BRAIN

Malignant migrating partial seizures in infancy: An epilepsy syndrome of unknown etiology

(2009) Giangennaro Coppola   EPILEPSIA

From EEG signals to brain connectivity: A model-based evaluation of interdependence measures

(2009) Fabrice Wendling et al.   JOURNAL OF NEUROSCIENCE METHODS

Epileptogenicity of brain structures in human temporal lobe epilepsy: a quantified study from intracerebral EEG

(2008) Fabrice Bartolomei et al.   BRAIN

Migrating Focal Seizures in Infancy: Analysis of the Electroclinical Patterns in 17 Patients

(2008) Roberto Horacio Caraballo et al.   JOURNAL OF CHILD NEUROLOGY