スポンサーリンク
Department of Pediatrics, School of Medicine, Fukuoka University | 論文
- 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
- 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
- Molecular Genetics of Human Familial Epilepsy Syndromes
- Genetic abnormalities underlying 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
- Long-Term Outcome of Treatment With Protocols AL841, AL851, and ALHR88 in Children With Acute Lymphoblastic Leukemia: Results Obtained by the Kyushu-Yamaguchi Children's Cancer Study Group
- Symptomatic Chiari Malformation and Associated Pathophysiology in Pediatric and Adult Patients without Myelodysplasia
- 術後口蓋裂児における裂型によることばの発達の差異
- OE-414 How TNFα Receptor Polyorphism Affect the State of Kawasaki Disease?(Congenital heart disease/Kawasaki's disease(01)(M),Oral Presentation(English),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
- Fc Gamma IIIa Receptor 158V/F Polymorphism and Kawasaki Disease(Congenital Heart Disease/Kawasaki's Disease 1 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Non-invasive Evaluation of Face and Motion Perception in Humans