スポンサーリンク
Department Of Cellular Physiology Graduate School Of Medicine Dentistry And Pharmaceutical Sciences | 論文
- PJ-015 Novel SCN5A Mutations Associated with Japanese Brugada Syndrome Patients(Arrhythmia, basic(04)(A),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
- Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome : pathological mutations and polymorphisms
- Analysis of Ictal EEGs of Epilepsy Associated with Tuberous Sclerosis
- Relationship between severity of epilepsy and developmental outcome in Angelman syndrome
- Is phenotype difference in severe myoclonic epilepsy in infancy related to SCN1A mutations?
- Paroxysmal movement disorders in severe myoclonic epilepsy in infancy
- IN B10 Paroxysmal movement disorder and severe myoclonic epilepsy in infancy
- Clinical and electroencephalographic characteristics of children with febrile seizures plus
- A population-based neuroepidemiological survey of West syndrome in Okayama Prefecture, Japan
- Long-Term Follow-Up of Childhood Epilepsy Associated with Tuberous Sclerosis
- A Cdk5 Inhibitor Enhances the Induction of Insulin Secretion by Exendin-4 Both in Vitro and in Vivo
- Nationwide survey (incidence, clinical course, prognosis) of Rasmussen's encephalitis