1. Mitochondrial myopathy with autophagic vacuoles in patients with the m.8344A>G mutation. Issue 8 (4th April 2013) Authors: Yuan, Jun-Hui; Sakiyama, Yusuke; Higuchi, Itsuro; Inamori, Yukie; Higuchi, Yujiro; Hashiguchi, Akihiro; Higashi, Keiko; Yoshimura, Akiko; Takashima, Hiroshi Journal: Journal of clinical pathology Issue: Volume 66:Issue 8(2013) Page Start: 659 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Multicenter questionnaire survey for sporadic inclusion body myositis in Japan. Issue 1 (December 2016) Authors: Suzuki, Naoki; Mori-Yoshimura, Madoka; Yamashita, Satoshi; Nakano, Satoshi; Murata, Ken-ya; Inamori, Yukie; Matsui, Naoko; Kimura, En; Kusaka, Hirofumi; Kondo, Tomoyoshi; Higuchi, Itsuro; Kaji, Ryuji; Tateyama, Maki; Izumi, Rumiko; Ono, Hiroya; Kato, Masaaki; Warita, Hitoshi; Takahashi, Toshiaki;... Journal: Orphanet journal of rare diseases Issue: Volume 11:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Novel mutations identified in patients with a mild phenotype of Ullrich congenital muscular dystrophy through targeted next‐generation sequencing. Issue 4 (26th August 2013) Authors: Yuan, Jun‐Hui; Higuchi, Itsuro; Sakiyama, Yusuke; Inamori, Yukie; Matsuura, Eiji; Higuchi, Yujiro; Yoshimura, Akiko; Saigo, Ryuji; Hashiguchi, Akihiro; Higashi, Keiko; Arimura, Kimiyoshi; Takashima, Hiroshi Journal: Neurology and clinical neuroscience Issue: Volume 1:Issue 4(2013:Jul.) Page Start: 148 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗