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European Consortium on the Genetics of Idiopathic Generalized Epilepsy | 論文
- Evidence for Linkage between Juvenile Myoclonic Epilepsy-Related Idiopathic Generalized Epilepsy and 6p11-12 in Dutch Families
- Exploration of a Putative Susceptibility Locus for Idiopathic Generalized Epilepsy on Chromosome 8p12
- Autosomal Recessive Idiopathic Epilepsy in an Inbred Family from Turkey : Identification of a Putative Locus on Chromosome 9q32-33
- Lack of SCN1A Mutations in Familial Febrile Seizures
- No Evidence of a Major Locus for Benign Familial Infantile Convulsions on Chromosome 19q12-q13.1
- Ictal Perfusion Changes During Occipital Lobe Seizures in Infancy : Report of Two Serial Ictal Observations
- Single-photon emission computed tomography : ictal perfusion in childhood epilepsies
- Topiramate Pharmacokinetics in Children with Epilepsy Aged from 6 Months to 4 Years
- The Nonmalformed Hemisphere Is Secondarily Impaired in Young Children with Hemimegalencephaly : A Pre- and Postsurgery Study with SPECT and EEG
- Monozygous Twin Brothers Discordant for Photosensitive Epilepsy : First Report of Possible Visual Priming in Humans
- Univerricht-Lundborg Disease : Underdiagnosed in the Netherlands
- Dravet syndrome : Early clinical manifestations and cognitive outcome in 37 Italian patients
- Replication Analysis of a Putative Susceptibility Locus (EGI) for Idiopathic Generalized Epilepsy on Chromosome 8q24
- Ictal EEG patterns in epilepsy with centro-temporal spikes