1. Antibodies against peptides of NMDA-type GluR in cerebrospinal fluid of patients with epileptic spasms. (November 2016) Authors: Mori, Tatsuo; Takahashi, Yukitoshi; Araya, Nami; Oboshi, Taikan; Watanabe, Hirokazu; Tsukamoto, Kazuki; Yamaguchi, Tokito; Yoshitomi, Shinsaku; Nasu, Hirosato; Ikeda, Hiroko; Otani, Hideyuki; Imai, Katsumi; Shigematsu, Hideo; Inoue, Yushi Journal: European journal of paediatric neurology Issue: Volume 20:Number 6(2016:Nov.) Page Start: 865 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Individualized Phenytoin Therapy for Japanese Pediatric Patients With Epilepsy Based on CYP2C9 and CYP2C19 Genotypes. Issue 2 (April 2015) Authors: Yamamoto, Yoshiaki; Takahashi, Yukitoshi; Imai, Katsumi; Miyakawa, Kou; Ikeda, Hiroko; Ueda, Yuki; Yamaguchi, Tokito; Nasu, Hirosato; Ohtani, Hideyuki; Shigematsu, Hideo; Kagawa, Yoshiyuki; Inoue, Yushi Journal: Therapeutic drug monitoring Issue: Volume 37:Issue 2(2015:Apr.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Somatic mosaic deletions involving SCN1A cause Dravet syndrome. Issue 3 (17th January 2018) Authors: Nakayama, Tojo; Ishii, Atsushi; Yoshida, Takeshi; Nasu, Hirosato; Shimojima, Keiko; Yamamoto, Toshiyuki; Kure, Shigeo; Hirose, Shinichi Journal: American journal of medical genetics Issue: Volume 176:Issue 3(2018) Page Start: 657 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗