Autosomal dominant nocturnal frontal lobe epilepsy : a genotypic comparative study of Japanese and Korean families carrying the CHRNA4 Ser284Leu mutation
スポンサーリンク
概要
- 論文の詳細を見る
- 2011-08-01
著者
-
Hirose Shinichi
Department Of Pediatrics School Of Medicine Fukuoka University
-
Hirose Shinichi
Department Of Biomolecular Engineering Graduate School Of Bioscience And Biotechnology Tokyo Institu
-
Kurahashi Hirokazu
Department Of Pediatrics Nagoya University Graduate School Of Medicine
-
Cho Yong-won
Department Of Neurology Dongsan Medical Center Keimyung University
-
MAKITA Yoshio
Education Center, Asahikawa Medical College
-
Hwang Su-kyeong
Department Of Pediatrics School Of Medicine Fukuoka University
-
Makita Yoshio
Education Center Asahikawa Medical University
-
Kurahashi Hirokazu
Department Of Pediatric Neurology Aichi Prefectural Colony Central Hospital
-
Hirose Shinichi
Department of Pediatrics, School of Medicine, Fukuoka University
関連論文
- 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)
- 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