スポンサーリンク
Department of Pediatrics, Faculty of Medicine, Fukuoka University | 論文
- Reperfusion Injury as a Complication Associated with Peripherally Inserted Central Catheters
- A Case of West Syndrome Associated with Neonatal Hypoglycemic Brain Injury
- 最近15年間に当科で経験した乳児脳腫瘍の予後と晩期障害
- A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions
- Mutations of Neuronal Voltage-gated Na^+ Channel α1 Subunit Gene SCN1A in Core Severe Myoclonic Epilepsy in Infancy (SMEI) and in Borderline SMEI (SMEB)
- II F10 A case of parietal lobe epilepsy with ictal smile
- Mutation screening of AP3M2 in Japanese epilepsy patients
- Ictal Midline Epileptiform Discharges in Benign Familial Neonatal Convulsions
- Genetics of Idiopathic Epilepsies
- The genetics of febrile seizures and related epilepsy syndromes
- IV B13 Sodium channel genes in patients following febrile seizures plus
- Genetics of epilepsy : current status and perspectives
- Molecular Genetics of Human Familial Epilepsy Syndromes
- Electroclinical Picture of Autosomal Dominant Nocturnal Frontal Lobe Epilepsy in a Japanese Family
- The effectiveness of clonazepam on the Rolandic discharges
- Japanese monozygotic twins with Rett syndrome
- F-waves in neonates : increased spinal anterior horn motor neuron excitability
- Bone lesions in elderly patients with multiple myeloma : a multicenter study by the Society for Geriatric Hematology
- Genome-wide identification of febrile seizure and related epilepsy phenotype loci
- Severe hyperbilirubinemia in a 10-year-old girl with a combined disorder of hereditary spherocytosis and Gilbert syndrome