[home]
[thesaurus]
Click Here to return To Results
Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006
See this aricle in Pubmed
Article Abstract
No abstract available for this article
Related Tags
(click to filter results - removes previous filter)
ataxia
cerebellar ataxia,children
children
chromosomal abnormality
chromosome 2
cognition
developmental retardation
Dravet syndrome
familial
fever
gene mutation
genetic neurologic disorders
intellectual deficit
mortality
myoclonic jerks
myoclonus
myoclonus,epilepsy
prognosis
psychomotor retardation
pyramidal tract dysfunction
review article
SCN1A gene
seizure
seizure,children
seizure,familial
seizure,febrile
seizure,intractable
seizure,neonatal
seizure,tonic-clonic
sodium channel dysfunction
status epilepticus
Click Here to return To Results