スポンサーリンク
福岡大学 医学部小児科 | 論文
- 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)
- 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 D6 How SCN1A mutations contribute to Dravet syndrome : a comparison of clinical and EEG features between Dravet syndrome with and without SCN1A mutations
- 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
- 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
- 消化管のビタミンD不応により新生児低Ca血症が遷延したと考えられた正期産不当軽量児の一例
- ウレアーゼ処理・GC/MS分析法による4-ヒドロキシ酪酸尿症の化学診断
- D-20 4-ヒドロキシ酪酸尿症(SSADH欠損症)の兄弟例
- 髄液より特異DNAが検出され, interleukin-6が高値を示したマイコプラズマ脳炎の1小児例
- E-18 急速進行性に脳萎縮を呈したEpilepsia Partialis Continua(EPC)の1例
- I-7 Myoclonic astatic epilepsy of early childhood (MAE) の脳波学的検討 : parietalθ(Doose) rhythmsの診断的意義
- F-12 Zonisamide(ZNS)による発汗減少から熱射病(Heat stroke)を呈した一例