1. 5‐Aminolevulinic acid can ameliorate language dysfunction of patients with ATR‐X syndrome. (16th January 2020) Authors: Wada, Takahito; Suzuki, Shuichi; Shioda, Norifumi Journal: Congenital anomalies Issue: Volume 60:Number 5(2020) Page Start: 147 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Analysis of triptan use during pregnancy in Japan: A case series. (13th January 2022) Authors: Yamaguchi, Yuko; Yamada, Takahiro; Goto, Mikako; Kawasaki, Hidenori; Wada, Takahito; Ikeda‐Sakai, Yasuko; Saito, Yoshiyuki; Hayashi, Masahiro; Tanaka, Shiro; Takahashi, Ryosuke; Nakayama, Takeo; Murashima, Atsuko; Kosugi, Shinji Journal: Congenital anomalies Issue: Volume 62:Number 2(2022) Page Start: 78 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Corrigendum to 'Novel gait training using a dual-belt treadmill in older adults: a randomized controlled trial' [Archives of Gerontology and Geriatrics 98 Jan-Feb (2021) 104573]. (March 2022) Authors: Wakida, Masanori; Mori, Kimihiko; Kubota, Ryo; Kuwabara, Takayuki; Mano, Naoto; Wada, Takahito; Taguchi, Meguru; Ohata, Koji; Yamada, Shigehito; Hase, Kimitaka Journal: Archives of gerontology and geriatrics Issue: Volume 99(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Current status and legal/ethical problems in the research use of the tissues of aborted human fetuses in Japan. (14th August 2020) Authors: Kawasaki, Hidenori; Yamada, Takahiro; Wada, Takahito; Kosugi, Shinji Journal: Congenital anomalies Issue: Volume 60:Number 6(2020) Page Start: 166 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Deletion of UBE3A in brothers with Angelman syndrome at the breakpoint with an inversion at 15q11.2. Issue 11 (6th August 2014) Authors: Kuroda, Yukiko; Ohashi, Ikuko; Saito, Toshiyuki; Nagai, Jun‐Ichi; Ida, Kazumi; Naruto, Takuya; Wada, Takahito; Kurosawa, Kenji Journal: American journal of medical genetics Issue: Volume 164:Issue 11(2014.) Page Start: 2873 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Delineation of the KIAA2022 mutation phenotype: Two patients with X‐linked intellectual disability and distinctive features. (21st April 2015) Authors: Kuroda, Yukiko; Ohashi, Ikuko; Naruto, Takuya; Ida, Kazumi; Enomoto, Yumi; Saito, Toshiyuki; Nagai, Jun‐ichi; Wada, Takahito; Kurosawa, Kenji Journal: American journal of medical genetics Issue: Volume 167:Number 6(2015:Jun.) Page Start: 1349 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Effect of ATRX and G‐Quadruplex Formation by the VNTR Sequence on α‐Globin Gene Expression. (20th April 2016) Authors: Li, Yue; Syed, Junetha; Suzuki, Yuki; Asamitsu, Sefan; Shioda, Norifumi; Wada, Takahito; Sugiyama, Hiroshi Journal: Chembiochem Issue: Volume 17:Number 10(2016) Page Start: 928 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Japanese familial case of myoclonus–dystonia syndrome with a splicing mutation in SGCE. Issue 2 (April 2015) Authors: Wada, Takahito; Takano, Kyoko; Tsurusaki, Yoshinori; Miyake, Noriko; Nakashima, Mitsuko; Saitsu, Hirotomo; Matsumoto, Naomichi; Osaka, Hitoshi Journal: Pediatrics international Issue: Volume 57:Issue 2(2015) Page Start: 324 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Novel gait training using a dual-belt treadmill in older adults: A randomized controlled trial. (January 2022) Authors: Wakida, Masanori; Mori, Kimihiko; Kubota, Ryo; Kuwabara, Takayuki; Mano, Naoto; Wada, Takahito; Taguchi, Meguru; Ohata, Koji; Yamada, Shigehito; Hase, Kimitaka Journal: Archives of gerontology and geriatrics Issue: Volume 98(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Phenotypic Spectrum of COL4A1 Mutations: Porencephaly to Schizencephaly. Issue 1 (7th December 2012) Authors: Yoneda, Yuriko; Haginoya, Kazuhiro; Kato, Mitsuhiro; Osaka, Hitoshi; Yokochi, Kenji; Arai, Hiroshi; Kakita, Akiyoshi; Yamamoto, Takamichi; Otsuki, Yoshiro; Shimizu, Shin‐ichi; Wada, Takahito; Koyama, Norihisa; Mino, Yoichi; Kondo, Noriko; Takahashi, Satoru; Hirabayashi, Shinichi; Takanashi, Jun‐i... Journal: Annals of neurology Issue: Volume 73:Issue 1(2013:Jan.) Page Start: 48 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗