Nature Search

Mutations of DEPDC5 cause autosomal dominant focal epilepsies

Stéphanie Baulac and colleagues report the identification of mutations in the DEPDC5 gene that cause focal epilepsies.

Saeko Ishida
Fabienne Picard
Stéphanie Baulac
Research31 Mar 2013
Nature Genetics

Volume: 45, P: 552-555
First genetic evidence of GABA_A receptor dysfunction in epilepsy: a mutation in the γ2-subunit gene

Stéphanie Baulac
Gilles Huberfeld
Eric LeGuern
Research01 May 2001
Nature Genetics

Volume: 28, P: 46-48
De novo mutations in HCN1 cause early infantile epileptic encephalopathy

Christel Depienne, Eric LeGuern and colleagues report the identification of 5 de novo missense mutations in HCN1 in individuals with early-onset epileptic encephalopathy. Functional studies confirmed the pathogenic nature of these mutations.

Caroline Nava
Carine Dalle
Christel Depienne
Research20 Apr 2014
Nature Genetics

Volume: 46, P: 640-645
Functional ultrasound imaging of the brain

A new method called functional ultrasound (fUS) is reported that allows imaging of transient changes in blood volume in the whole rat brain with a spatiotemporal resolution not attained by other functional brain imaging modalities.

Emilie Macé
Gabriel Montaldo
Mickael Tanter
Research03 Jul 2011
Nature Methods

Volume: 8, P: 662-664
Glutamatergic pre-ictal discharges emerge at the transition to seizure in human epilepsy

Brief and synchronous inter-ictal events can occur between seizures. Using human tissue samples and electroencephalography, this study shows that the transition from pre-ictal discharge to ictal discharge involves distinct temporal and spatial characteristics as well as glutamatergic mechanisms.

Gilles Huberfeld
Liset Menendez de la Prida
Richard Miles
Research03 Apr 2011
Nature Neuroscience

Volume: 14, P: 627-634
Voluntary control of intracortical oscillations for reconfiguration of network activity

Juliana Corlier
Mario Valderrama
Michel Le Van Quyen
ResearchOpen Access03 Nov 2016
Scientific Reports

Volume: 6, P: 1-15
Cognitive dissonance resolution depends on episodic memory

Mariam Chammat
Imen El Karoui
Lionel Naccache
ResearchOpen Access23 Jan 2017
Scientific Reports

Volume: 7, P: 1-10

Quick links

Search

Mutations of DEPDC5 cause autosomal dominant focal epilepsies

First genetic evidence of GABA_A receptor dysfunction in epilepsy: a mutation in the γ2-subunit gene

De novo mutations in HCN1 cause early infantile epileptic encephalopathy

Functional ultrasound imaging of the brain

Glutamatergic pre-ictal discharges emerge at the transition to seizure in human epilepsy

Voluntary control of intracortical oscillations for reconfiguration of network activity

Cognitive dissonance resolution depends on episodic memory

Search

Quick links

Search

Filter By:

Mutations of DEPDC5 cause autosomal dominant focal epilepsies

First genetic evidence of GABAA receptor dysfunction in epilepsy: a mutation in the γ2-subunit gene

De novo mutations in HCN1 cause early infantile epileptic encephalopathy

Functional ultrasound imaging of the brain

Glutamatergic pre-ictal discharges emerge at the transition to seizure in human epilepsy

Voluntary control of intracortical oscillations for reconfiguration of network activity

Cognitive dissonance resolution depends on episodic memory

Search

Quick links

First genetic evidence of GABA_A receptor dysfunction in epilepsy: a mutation in the γ2-subunit gene