Results 181 to 186 of about 8,423 (186)

Electroencephalographic features of patients with SCN1A-positive Dravet syndrome

Brain and Development, 2015
Ching-Shiang Chi, Ching-Shiang Chi
exaly  

Nonfunctional SCN1A Is Common in Severe Myoclonic Epilepsy of Infancy

Epilepsia, 2006
Iori Ohmori, Alfred L George, Kristopher M Kahlig   +2 more
exaly  

Clinical spectrum of SCN1A mutations

Epilepsia, 2009
Antonio Gambardella, Carla Marini
exaly  

The SCN1A Mutation Database: Updating Information and Analysis of the Relationships among Genotype, Functional Alteration, and Phenotype

Human Mutation, 2015
Wei-Ping Liao, Xiaorong Liu, Yue-Sheng Long   +2 more
exaly  

Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome.

Brain, 2012
exaly  

Panayiotopoulos syndrome: Probable genetic origin, but not in SCN1A

European Journal of Paediatric Neurology, 2011
exaly