1. Bilateral striatal lesions in a family with mitochondrial 14459G>A mutation. Issue 6 (28th October 2014) Authors: Nishijima, Haruo; Tomiyama, Masahiko; Nishi‐ie, Yurie; Funamizu, Yukihisa; Miki, Yasuo; Kurihara, Ai‐ichiro; Goto, Yu‐ichi Journal: Neurology and clinical neuroscience Issue: Volume 2:Issue 6(2014:Nov.) Page Start: 213 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Concise Review: Heteroplasmic Mitochondrial DNA Mutations and Mitochondrial Diseases: Toward iPSC‐Based Disease Modeling, Drug Discovery, and Regenerative Therapeutics. (13th February 2016) Authors: Hatakeyama, Hideyuki; Goto, Yu‐ichi Journal: Stem cells Issue: Volume 34:Number 4(2016:Apr.) Page Start: 801 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. COX6A2 variants cause a muscle‐specific cytochrome c oxidase deficiency. Issue 2 (2nd July 2019) Authors: Inoue, Michio; Uchino, Shumpei; Iida, Aritoshi; Noguchi, Satoru; Hayashi, Shinichiro; Takahashi, Tsutomu; Fujii, Katsunori; Komaki, Hirofumi; Takeshita, Eri; Nonaka, Ikuya; Okada, Yukinori; Yoshizawa, Takuya; Van Lommel, Leentje; Schuit, Frans; Goto, Yu‐ichi; Mimaki, Masakazu; Nishino, Ichizo Journal: Annals of neurology Issue: Volume 86:Issue 2(2019) Page Start: 193 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. ECHS1 Mutations Cause Combined Respiratory Chain Deficiency Resulting in Leigh Syndrome. Issue 2 (February 2015) Authors: Sakai, Chika; Yamaguchi, Seiji; Sasaki, Masayuki; Miyamoto, Yusaku; Matsushima, Yuichi; Goto, Yu‐ichi Journal: Human mutation Issue: Volume 36:Issue 2(2015:Feb.) Page Start: 232 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Higd1a improves respiratory function in the models of mitochondrial disorder. Issue 1 (10th December 2019) Authors: Nagao, Takemasa; Shintani, Yasunori; Hayashi, Takaharu; Kioka, Hidetaka; Kato, Hisakazu; Nishida, Yuya; Yamazaki, Satoru; Tsukamoto, Osamu; Yashirogi, Shohei; Yazawa, Issei; Asano, Yoshihiro; Shinzawa‐Itoh, Kyoko; Imamura, Hiromi; Suzuki, Takeo; Suzuki, Tsutomu; Goto, Yu‐ichi; Takashima, Seiji Journal: FASEB journal Issue: Volume 34:Issue 1(2020) Page Start: 1859 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Identification of two novel Shank3 transcripts in the developing mouse neocortex. (14th November 2013) Authors: Waga, Chikako; Asano, Hirotsugu; Sanagi, Tomomi; Suzuki, Eri; Nakamura, Yasuko; Tsuchiya, Akiko; Itoh, Masayuki; Goto, Yu‐ichi; Kohsaka, Shinichi; Uchino, Shigeo Journal: Journal of neurochemistry Issue: Volume 128:Number 2(2014:Jan.) Page Start: 280 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Isolated mitochondrial stroke‐like episodes in an elderly patient with the MT‐ND3 gene mutation. Issue 4 (17th March 2015) Authors: Mukai, Masako; Sugaya, Keizo; Ozawa, Tadashi; Goto, Yu‐ichi; Yagishita, Akira; Matsubara, Shiro; Bokuda, Kota; Miyakoshi, Akinori; Nakano, Imaharu Journal: Neurology and clinical neuroscience Issue: Volume 3:Issue 4(2015) Page Start: 153 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Magnetic resonance imaging findings in Leigh syndrome with a novel compound heterozygous SURF1 gene mutation. Issue 1 (17th December 2015) Authors: Kim, Younhee; Koide, Reiji; Isozaki, Eiji; Goto, Yu‐ichi Journal: Neurology and clinical neuroscience Issue: Volume 4:Issue 1(2016:Jan.) Page Start: 34 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Mitochondrial Complex III Deficiency Caused by a Homozygous UQCRC2 Mutation Presenting with Neonatal‐Onset Recurrent Metabolic Decompensation. Issue 3 (29th January 2013) Authors: Miyake, Noriko; Yano, Shoji; Sakai, Chika; Hatakeyama, Hideyuki; Matsushima, Yuichi; Shiina, Masaaki; Watanabe, Yoriko; Bartley, James; Abdenur, Jose E.; Wang, Raymond Y.; Chang, Richard; Tsurusaki, Yoshinori; Doi, Hiroshi; Nakashima, Mitsuko; Saitsu, Hirotomo; Ogata, Kazuhiro; Goto, Yu‐ichi; Mat... Journal: Human mutation Issue: Volume 34:Issue 3(2013:Mar.) Page Start: 446 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Nervonic acid level in cerebrospinal fluid is a candidate biomarker for depressive and manic symptoms: A pilot study. Issue 4 (18th February 2021) Authors: Kageyama, Yuki; Deguchi, Yasuhiko; Hattori, Kotaro; Yoshida, Sumiko; Goto, Yu‐ichi; Inoue, Koki; Kato, Tadafumi Journal: Brain and behavior Issue: Volume 11:Issue 4(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗