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Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions.
Ono S, Yoshiura K, Kinoshita A, Kikuchi T, Nakane Y, Kato N, Sadamatsu M, Konishi T, Nagamitsu S, Matsuura M, Yasuda A, Komine M, Kanai K, Inoue T, Osamura T, Saito K, Hirose S, Koide H, Tomita H, Ozawa H, Niikawa N, Kurotaki N. Ono S, et al. Among authors: sadamatsu m. J Hum Genet. 2012 May;57(5):338-41. doi: 10.1038/jhg.2012.23. Epub 2012 Mar 8. J Hum Genet. 2012. PMID: 22399141
Comparison of pervasive developmental disorder and schizophrenia by the Japanese version of the National Adult Reading Test.
Ota T, Iida J, Sawada M, Suehiro Y, Kishimoto N, Tanaka S, Nagauchi K, Nakanishi Y, Yamamuro K, Negoro H, Iwasaka H, Sadamatsu M, Kishimoto T. Ota T, et al. Among authors: sadamatsu m. Int J Psychiatry Clin Pract. 2013 Feb;17(1):10-5. doi: 10.3109/13651501.2011.653380. Epub 2012 Feb 15. Int J Psychiatry Clin Pract. 2013. PMID: 22335467
Demyelination in the juvenile period, but not in adulthood, leads to long-lasting cognitive impairment and deficient social interaction in mice.
Makinodan M, Yamauchi T, Tatsumi K, Okuda H, Takeda T, Kiuchi K, Sadamatsu M, Wanaka A, Kishimoto T. Makinodan M, et al. Among authors: sadamatsu m. Prog Neuropsychopharmacol Biol Psychiatry. 2009 Aug 31;33(6):978-85. doi: 10.1016/j.pnpbp.2009.05.006. Epub 2009 May 14. Prog Neuropsychopharmacol Biol Psychiatry. 2009. PMID: 19446597
37 results