Channelopathies in Idiopathic Epilepsy
Open Access
- 1 April 2007
- journal article
- review article
- Published by Elsevier BV in Neurotherapeutics
- Vol. 4 (2), 295-304
- https://doi.org/10.1016/j.nurt.2007.01.009
Abstract
No abstract availableKeywords
This publication has 110 references indexed in Scilit:
- SCN1A Mutation Mosaicism in a Family with Severe Myoclonic Epilepsy in InfancyEpilepsia, 2006
- Increased Sensitivity of the Neuronal Nicotinic Receptor α2 Subunit Causes Familial Epilepsy with Nocturnal Wandering and Ictal FearAmerican Journal of Human Genetics, 2006
- Infantile seizures and other epileptic phenotypes in a Chinese family with a missense mutation of KCNQ2European Journal of Pediatrics, 2006
- Genetic dissection of the common epilepsiesCurrent Opinion in Neurology, 2006
- Somatic and germline mosaicisms in Severe Myoclonic Epilepsy of InfancyBiochemical and Biophysical Research Communications, 2006
- The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficitsNeurobiology of Disease, 2005
- Variations on an inhibitory theme: phasic and tonic activation of GABAA receptorsNature Reviews Neuroscience, 2005
- Seizure phenotypes of a family with missense mutations in SCN2APediatric Neurology, 2004
- Complete Loss of the Cytoplasmic Carboxyl Terminus of the KCNQ2 Potassium Channel: A Novel Mutation in a Large Czech Pedigree with Benign Neonatal Convulsions or Other Epileptic PhenotypesEpilepsia, 2004
- Epilepsies in twins: Genetics of the major epilepsy syndromesAnnals of Neurology, 1998