1) 麻生幸三郎:神経細胞の移動障害とてんかん.脳と発達 29:129-133, 1997
2) Barkovich AJ, Kuzniecky RI, Jackson GD, et al:A developmental and genetic classification for malformations of cortical development. Neurology 65:1873-1887, 2005
3) Honavar M, Meldrum BS:Epilepsy. In:Graham DI, Landtos FL eds. Greenfield's Neuropathology, 7th ed. Arnold, London. pp905-908, 2002
4) Jansen A, Andermann E:Genetics of polymicrogyria syndromes. J Med Genet 42:369-378, 2005
5) Kuzniecky R, Andermann F, Guerrini R:Congenital bilateral perisylvian syndrome:Study of 31 patients. The CBPS multicenter collaborative study. Lancet 341:608-612, 1993
6) Lyseng-Williamson KA:Sitagliptin. Drugs 67:2231-2256, 2007
7) Maeda T, Akaishi M, Shimizu M, et al:The subclassification of schizencephaly and its clinical characterization. Brain Dev 31:694-701, 2009
8) 松田希,松田俊枝,本間真理,他:Congenital bilateral perisylvian syndromeの成人軽症例.神経内科 68:513-514, 2008
9) 松田一巳,八木和一:トピラマート(KW-6485)の症候性局在関連性てんかんに対する第Ⅲ相臨床試験―プラセボを対照とした二重盲検並行群間比較試験.新薬と臨牀56:1385-1403, 2007
10) 三原忠紘,松田一巳:脳の働きをうかがい知る外科てんかん学入門.創造出版,pp57-72, 2008
11) Sebire G, Husson B, Dusser A, et al:Congenital unilateral perisylvian syndrome:Radiological basis and clinical correlations. J Neurol Neurosurg Psychiatry 61:52-56, 1996
12) Sejima H, Takusa Y, Kimura M, et al:A variant case of congenital bilateral perisylvian syndrome with asymmetric findings on neuroimaging and septum pellucidum defect. Brain Dev 23:131-134, 2001
13) Shorvon S:Handbook of Epilepsy Treatment. Second Edition. Blackwell Publishing, Oxford, pp60-113, 2005