IV D6 How SCN1A mutations contribute to Dravet syndrome : a comparison of clinical and EEG features between Dravet syndrome with and without SCN1A mutations
スポンサーリンク
概要
- 論文の詳細を見る
- 日本てんかん学会の論文
- 2002-09-11
著者
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Hirose Shinichi
Department Of Pediatrics Faculty Of Medicine Fukuoka University
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Hirose Shinichi
福岡大学 医学部小児科
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Oguni Hirokazu
The Department of Pediatrics, Tokyo Women's Medical University
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Awaya Yutaka
The Department of Pediatrics, Seibo International Catholic Hospital
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Osawa Makiko
The Department of Pediatrics, Tokyo Women's Medical University
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Fukuma Goryu
The Department of Pediatrics, School of Medicine, Fukuoka University
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Hirose Shinichi
The Department of Pediatrics, School of Medicine, Fukuoka University
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Mitsudome Akihisa
The Department of Pediatrics, School of Medicine, Fukuoka University
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Kaneko Sunao
The Department of Neuropsychiatry, School of Medicine, Hirosaki University
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Kaneko Sunao
Department Of Neuropsychiatry School Of Medicine Hirosaki University
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Fukuma Goryu
Department Of Pediatrics School Of Medicine Fukuoka University
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Hirose Shinichi
Department Of Pediatrics School Of Medicine Fukuoka University
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Oguni Hirokazu
Department Of Pediatrics School Of Medicine Tokyo Women's Medical University
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Ogata Hiroko
Department Of Pediatrics Tokyo Women's University
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Oosawa Makiko
Department Of Pediatrics Tokyo Women's Medical University
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Oguni Hirokazu
Department Of Pediatrics Tokyo Women's Medical Cillege
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Saito Kayoko
Department Of Neuropsychiatry School Of Medicine Hirosaki University
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Osawa Makiko
Department Of Pediatrics Tpkyo Woman's Medical College
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Osawa Makiko
Department Of Pediatrics Tokyo Woman's Medical University
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Shiraishi Hideyuki
Department Of Pediatrics Kyoto University Faculty Of Medicine
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Awaya Yutaka
Department of Pediatrics, Seibo International Catholic Hospital
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