浜崎 雄平 | Department of Pediatrics, Saga Medical School
スポンサーリンク
概要
Department of Pediatrics, Saga Medical School | 論文
- Mutations of Neuronal Voltage-gated Na^+ Channel α1 Subunit Gene SCN1A in Core Severe Myoclonic Epilepsy in Infancy (SMEI) and in Borderline SMEI (SMEB)
- Detection of immunodeficiencies and persistent infections by urinary neopterin measurement
- Classic Rett syndrome in a boy with R133C mutation of MECP2
- Autoimmune Neutropenia of Infancy with Multiple Brain Abscesses during the Course of Human Herpesvirus-6 Infection
- Extensive white matter involvement in hemorrhagic shock and encephalopathy syndrome